Method of producing derivatives of cyclic amine or their acid-additive salts

专利摘要:
Cyclic amine derivatives of the formula <IMAGE> in which A, B, E, G, R, R1, R2, m and n are as defined in Claim 1, their enantiomers, their diastereomers, their N-oxides and their acid addition salts have useful pharmacological properties, in particular a bradycardic action. The novel compounds can be prepared by processes known per se.
公开号:SU1561823A3
申请号:SU884355736
申请日:1988-05-24
公开日:1990-04-30
发明作者:Хейдер Иоахим；Псиошь Манфред；Бомхард Андреас；Хауель Норберт；Нарр Бертольд；Нолл Клаус；Лиллие Кристиан；Кобингер Вальтер；Деммген Юрген
申请人:Др.Карл Томэ Гмбх (Фирма)；
IPC主号:

专利说明:

batching refers to the production of cyclic amine derivatives of the formula
CHN-E B
/ №g} t
SNHB-ЈХН2) C)
de a
-sn "-sn"
at
E
R
R group -CH, or
a -CH2, CH2CI2-, -CO or -CHiCO- group, with the x carbon atom bound to the phenyl prom; unbranched alkylene with i 3 carbon atoms8 unsubstituted or substituted by alkyl with 1-3 carbon atoms; alkylene with 1-6 carbon atoms; , iKa lower alkyl or lower alkox group, or together, they form a methylenedioxy group; naphthyl or naphthyloxy, unsubstituted or mono- FPI disubstituted by lower alkyl or alkoxy, benziloksig group, drilled, thienyl, chndo- lil, pyridyl, unsubstituted or substituted by lower alkyl, isoquinolyl, substituted with two lower alkoxy Rupp, benzoPe furyl or unsubstituted benzoG tienil9 or substituted by lower alkoxyl or methylsulfoxyloxy, or phenyl, substituted by nitro, amino, acetylamino, lower alkyl or lower alkoxy, phenyl, substituted by two lower alkoxy groups or one methylenedioxy group, a fekoxy group substituted by a lower alkyl or a lower alkoxy group, a phenoxy group 3 substituted by a single methylenedioxy group or two lower alkyl or alkoxy groups or two halogen atoms, an anilino group substituted by two lower alkyl or alkoxy groups, a substituted one atom, another alkyl, when In means the group-CRj or -CO-,
0
five
0
five
0
five
0
five
m is 19 2., 3.4, b or 6; n is 0, 1, 2 or 3, and the sum m + n should be 3,4,5 or 6,
or their acid addition salts, which have the property of reducing the heart rate and reducing the need for heart rate.
The purpose of the invention is to develop, on the basis of known methods, a method for obtaining new compounds with valuable pharmacological properties with improved activity.
The invention is illustrated by the following winners.
Example 1. 2- (N- (3- (naphthyl-2) -propyl) -piperidyl-3) -methyl 3 hydrochloride 6 3 7 dimethoxy 1-oxo 1,2,3 94-TeTparHflt30-H3oxHHojxHHa.
A mixture of i g (3.2 mml) 2- (piperidyl 3 methyl) -L37-dimethoxy-1 oxo-1E2,3.4-tetrahydro-isoquinoline, 5 ml dimethyl sulfoxide 5 0 S5 g (0} 36 mmol potassium carbonate and 0.75 g (3.66 mmol) of 2- (3-chloropropyl) naphthblin is heated to 120 ° C for Jh.The reaction mixture is poured onto ice-water and shaken with 50 ml of ethyl acetate of three times, respectively. The combined organic phases are washed 2 M sodium hydroxide solution and water, dried over magnesium sulfate, concentrated in vacuo and the resulting residue is purified on silica gel (0.063 - 0S2 mm using 1% ethanol in methylene chloride). loride). The hydrochloride is dissolved in acetone, the hydrochloride is added with the addition of a hydrochloric acid and crystallized out with HS acetone.
Yield 0.74 g (4% of theoretical), so pl. 179-181 ° C.
Calculated,%: C, 70.77; H, 7.37; N 5.50; C1 6.96.
Found,%: C, 70.47; H 7.40; N 5.47; CI 7.06.
Example 2C Dihydrochloride 2- (N- (2- (4-aminophenyl) ethyl) piperidyl-3) methyl 5,6-dimethoxy-1-oxo-1,3-dihydrosoindole.
2.1 g of 978 mmol) 2 ™ (N- (2- (4- nor grophenyl) -ethyl) -piperidyl-3) me, 6-dimethoxy-1-oxo-1,3 cyhydro ™ ieoindole is dissolved in 50 ml of glacial acetic acid and with stirring, 0.4 ply (8.22 mmol) of hydrazine hydrate and a small amount of Rene nickel are added. Addition of 0.2 ml of hydrazine hydrate and correspondingly a small amount of Rene nickel is repeated three times after 60 minutes. The catalyst is removed from the catalyst, washed with methanol, the filtrate is dried under magnesium sulfate, concentrated in vacuo, and the resulting residue is purified on alumina (neutral, activity 11) with methylene chloride and then increasing amounts of ethanol.
Yield 1.8 g (91.8% of theory), 1 g is dissolved in acetone and dihydrochloride is added by addition of hydrochloric acid ether.
Output 1.02 g (86.4% of theoretical, in terms of base), so pl. 232 235 ° C.
Calculated,%: C 59.72; H 6.89; N 8.71; C1 14.69.
Found,%: C 59.54; H 7.08; N 8.56; C1 14.45.
EXAMPLE 3 2- (M- (2- (4-acetates) Absorbed from catalyst, concentrated and purified on a silica gel column using tylene chloride and methanol as eluene. Hydrochloric acid was extracted with hydrochloric acid and extracted from acetone.
Output 0.50 g (11% of theoretical 10 anyone), so pl. 204-20b ° C.
Calculated,%: C, 64.85; H 7.6 N 6.05; C1 7.66.
Found,%: C 64.88; H 7.76; N 5, ultrasound; C1 7.5b.
15 R value, 0.69 (silica gel, chloride chloride and methanol in a ratio of 10: 1; ammonia atmosphere).
PRI me R 5. Hydrochloride 2 (4- (naphthyl-2-hydroxy) -butyl) -pyrrole 20 3) methyl-6,7-dimethyl-1-oxo-1,2 tetrahydro from oquinoline.
Prepared from 2- (pyrrolidyl-3-m 6,7-dimethyl-1-oxo-1,2,3,4-tetra-ro-isoquinoline and 2- (4-bromo-butyl
thirty
min-phenyl) -ethyl) -piperidyl-3) -methyl-25 naphthalene as in Example 1. 5,6-dimethoxy-1-ox-1,3-dihydro-isoindole.
K 819 mg (2 mmol) 2- (H- (2- (4-amino-phenyl) -ethyl) -pyleridyl- 3) methyl 5, b-dimethoxy-1-roKco-1, 3-dihydro- isoindole in 10 ml of methylene chloride, after adding -0.3 ml (2.2 mmol) of triethylamine, 0.16 ml (2.2 mmol) of acetyl chloride was added dropwise. Thereby, the reaction temperature rises to 30 ° C. Stir for 30 minutes at room temperature, shake twice with water, dry the organic phase over magnesium sulfate and concentrate in vacuo. The residue is crystallized from acetone.
The output of 66Q mg (73.2% of theoretical), so pl, 195-196 ° C,
Calculated,%: C 69.16; H 7.37; N 9.31.
Found,%: C 69.33; H 7.11; N 9.16.
PRI me R 4. Hydrochloride 3- (N- (3- (furyl-2) -propyl) -piperidyl-3) - methyl-7,8-dimethoxy-2-oxo-1,3,4,5 - tetrahydro-2H-3-benzazepine,
3.2 g (0.010 mol) of 3- (piperidshg-3) -methyl-7,8-dimethoxy-2-oxo-t, 3,4, 5-tetragilro-2H 3-benzazepine in those
Output 3 (J% of theoretical, 133-136 ° -C.
Calculated,%: C, 67.02; H 6.9 N 5.21; Cl 14.86.
Found,%: C 67.26; H 7.03 N 5.36; C1 14.89.
Example 6. Hydrochloride 2 (2-methyl- (naphth-1) -methyl) -pyrodil-3) -methyl-6,7-dimethyl-1-ox about 35 1,2,3,4-tetrahydro-isoquinoline .
Prepared from 2-Spirrolidyl-Z-m 6,7-dimethyl-1-oxo-1,2,3,4-tetra-ro-isoquinoline and 1-chloromethyl-2-m naphthalene as in Example 1.
40
The output of 32.5% of theoretical so pl. 142-144 ° C.
Calculated: C, 69.34; H 7.6 N 5.77; C1 7.37.
45 Found: C 69.59; H 7.63; N 5.72; C1 7.89. PRI me R 7
50
Hydrobromide 2 (2- (5-methyl-6-methoxy-naphthyl 2) pyrrolidyl-3) methyl-6,7-dimethyl oxo-1,2,3,4-tetrahydro-from ochinol
Prepared from (pyrrolidylmethyl / -6,7-dimethyl-1-oxo-1,2,3 tetrahydro-isoquinoline and 2- (2-ethyl) -b-methyl-6-methoxy-naphthalene
The catalyst is filtered off with suction, concentrated and purified on a silica gel column using methylene chloride and methanol as eluent. The hydrochloride is isolated by the addition of simple ether hydrochloric acid and is crystallized from acetone.
Output 0.50 g (11% of theoretical), so pl. 204-20b ° C.
Calculated,%: C, 64.85; H 7.62; , N 6.05; C1 7.66.
Found,%: C 64.88; H 7.76; N 5, ultrasound; C1 7.5b.
R, 0.69 (silica gel, methylene chloride, and methanol in a ratio of 10: 1; ammonia atmosphere).
PRI me R 5. Hydrochloride 2 (N- (4- (naphthyl-2-hydroxy) -butyl) -pyrrolidyl-3) -methyl-6,7-dimethyl-1-oxo-1,2,3, 4- tetrahydro-from oquinoline.
Prepared from 2- (pyrrolidyl-3-methyl) 6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (4-bromo-butyloxy naphthalene as in Example 1.
naphthalene analogously to example 1.
Output 3 (J% of theoretical, mp. 133-136 ° -C.
Calculated,%: C, 67.02; H 6.92; N 5.21; Cl 14.86.
Found,%: C 67.26; H 7.03; N 5.36; C1 14.89.
Example 6: (2-Methyl- (naphth-1) -methyl) -pyrrolidyl-3) -methyl-6,7-dimethyl-1-ox-o-1,2,3,4-tetrahydro-isoquinoline hydrochloride.
Prepared from 2-Spirrolidyl-3-methyl) -6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloromethyl-2-methyl naphthalene analogously to Example 1.
Output 32.5% of theoretical, so pl. 142-144 ° C.
Calculated: C, 69.34; H 7.69; N 5.77; C1 7.37.
Found,%: C 69.59; H 7.63; N 5.72; C1 7.89. PRI me R 7
Hydrobromide 2Ј (N (2- (5-methyl-6-methoxy-naphthyl 2) ethyl) pyrrolidyl- 3) methyl-6,7-dimethyl ° 1 - oxo-1,2,3,4-tetrahydro from oquinoline .
Prepared from (pyrrolidyl-3-methyl / -6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (2-bromo-ethyl) -b-methyl-6-methoxy- naphthalene knowing
for 2 days, hydrogenation is carried out with 5g as in Example 1.
in 100 ml of absolute ethanol in when Yield 19% of theoretical, so pl,
In the absence of 1.3 g (.0.010 mol) of 3-furyl2-propanol and 1 g of Rene nickel at
230-232 ° C.
Calculated,%: C, 67.02; H 6.93; N 5.21; Br 14.86.
temperature 80 С and pressure 5 bar.
 Yield 19% of theoretical, etc.
230-232 ° C.
Calculated,%: C, 67.02; H 6.93; N 5.21; Br 14.86.
Found,%: C 67.10; H 7.12; N 5.33; Br 15.01.
Example Hydrochloride 2 $ N- (2, - (naphthyl-2) -ethyl) -pyrrolidyl-3) me-, 7-dimethoxy-1 oxo-71,2,3,4 tetrahydro-Ioquinoline.
Prepared from 2- (pyrrolidyl-J-methyl) 6,7-dimethoxy-1-oxo-1,2,3,4-tetra-hydro-isoquinoline and 2- (2-bromoethyl,) - naphthalene as in Example 1.
The output of 7.8% of theoretical, so pl. 219,221 ° C.
Calculated (xH40),%: C 67.39; H 7.07; N 5.61; C1 7.10.
Found,%: C 67.21; H 7.23; N 5.57; C1 7.63.
EXAMPLE 2-J4N- (2- (6-methoxy-naphthyl-2) -ethyl) -pyrrolidyl-3) methyl-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro hydrochloride isoquinoline.
Prepared from 2- (pyrrolidyl-3-me-, 7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline, and 2- (. 2-bromo-ethyl) -6-methoxy-naphthalene analogously to Example 1.
Output 39.2% of theoretical1, so pl. 224-226 ° C.
Calculated (x H2OJ,%: C 65.84; H 7.05; N 5.29; C1 7.05; N;
Found,%: C 66.08; H 7.13; N 5.39; C1 6.77.
Example 10. Hydrochloride (Y- (3-naphthyl 2-hydroxy) propyl) -piperidyl-2) ethyl-6,7-methylenedioxy-1-oxy-1,2,3,4-tetrahydro-isoquinoline .
Prepared from 2- (piperidyl-2) -etchg 6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (3-chloro-nponoKCHj-naphthalene, as in Example 1.
The output of 21.2% of theoretical, so pl. 85-875С.
Calculated (x H20)%: C, 66.59; H 6.89; N 5, 6.5J.
Found, 7 ,: С 66.77; H 6.89; N 4.95; C1 6.74.
PRI mme R 11. Hydrochloride 2- 2- (No.- (2- (6-methoxy-naphthyl-2) -ethyl) -pyridyl-2) -ethyl-6,7 methylenedioxy-1-oxo-1 , 2,3,4-tetrahydro-isoquinoline.
Ethyl 1 -6., 7-methylenedioxy-1-oxo-1,2,3 4-tetrahydro-isoquinoline and 2 (2-bromo ethyl) -6-methoxy-naphthalene are obtained from (piperidyl-2) analogously to Example 1.
EXAMPLE 12 2-CM (. 2- (naphthyl-1) -ethyl) -piperidyl-3-methyl 3, 7-dimethoxy-1-oxo-1,2,3,4-hydrochloride hydrochloride isoquinoline.
Prepared from 2- (gosheridyl-3) -methyl-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2-ethyl-Saphyl-1) benzene-sulphonic acid ester analogously to Example 1.
Yield 26.9% of the theoretical. 220-2254,
Calculated,%: C, 67.89; H 7.27; . 5.46; C1 6.91.
Found,%: C 67.75; H 6.92; N 5.56; C1 7.00 „
PRI me R 13. Hydrochloride 2- (N- (2- (naphthyl-2) -ethyl) -pilyl-3) -methyl; -6,7-methylenedioxy-1-oxo-1,2 , 3, 4-tetrahydro-iooquinoline.
Prepared from 2- (piperidyl-3) -methyl-6,7-methylenedioxy 1-goxo-1,2,3, 4-tetrahydro-isoquinoline and 2-ethyl- (naphthyl-2) ester of benzenesulfonic acid as in example 1.
The output of 27.9% of theoretical, so pl. 128-130 ° C.
Calculated, (xH40),%: from 67.66; H 6.69; N 5.63; C1 7.13.
Found,%: C 67.64; H 6.70; N 5.76; C1 7.35
And p). 14. Hydrochloride 2 - (, H- (2- (5-methyl-6-label of sinanethyl-2).-E-tyl) - piperidyl-3) -methylT-6,7- methylenedio C-1-oxo-1,2,3,4-tetrahydroisoquinoline.
Prepared from 2- (piperidyl-3) -methyl-1-b, 7-methylenedioxy-t-oKco-1,2,3, 4-tetrahydro-isoquinoline and 2- (.2-bromo-ethyl) -5-methyl -6-methoxy-naphthalene analogously to example 1.
The output of 51.2% of theoretical, so pl. 128-131 ° C.
Calculated,%: C 68.88; H 6.74; N 5.34; C1 6.77.
Found%: C 68.90 j H 6.61; N 5.30; C1 7.05.
Example 15. 2- (N- ((2-methyl naphthyl-1) -methyl) -piperidyl-3) -methyl-6,7-dimethoxy-1-oxo-1,2,3, 4-tetrahydro-isoquinoline hydrochloride .
Prepared from 2-Spiperidyl-3) -me-, 7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloromethyl-2-methyl-naphthalene as in Example 1.
The output of 57.9% of theoretical, so pl. 212 214 ° C.
Calculated (xH40),%: C 67.63; H 7.63; N 5.44; C1 6, a8.
Found,%: C 67.46} H, 7.56; N 5.54; C1 6.67.
EXAMPLE 16 2- (N (4 (naphthyl-2 oxy) -butyl) -piperidyl 3) -methyl-6,7-dimethoxy-1-oxo-1,2,3 4 ™ tetrahydroisohiiioline hydrochloride .
Prepared from 2 chpkperidil 3 methi 6,7-dimethoxy 1 oxo 1,2,3,4 tetrahydroisoquinoline and 2- (4-bromo blu) si-naphthalene as in Example 1
Output 4b, 3 / o from theoretical, Toll. 80-84 ° L.
Calculated (x HgO),%: C, 66.83; H 7.41; N 5.03; CI 6.36.
Find%: C 66.79; H 7.22; N 4.90; Ci 6.64,
Example 17. Hydrochloride (2- (6-methoxy-naphthyl-2) -ethyl) - liperyl-3) methyl 6, / dimethoxy-1 ° oxo-1,2,3,4-tetrahydro-isoquinoline.
Receives from I Xpiperidyl-3) meth, 7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2 (ethyl) -6 methoxy naphthalene analogously to example 1.
The output of 2.8% of theoretical, t, pl. ,
Calculated, (x NaO h HC1 x x CH3COCH),%: C 64.01; H 7.65; N 4.52; C1 5.72.
Found,%: C 64.26; H 7.70; N 4.62; Ci 5.49.
Example 18. 18. (N- (2- (6 Methoxy-naphthyl 2) -ethyl) pilyridyl-3. Propyl 6.7 methylenedioxy-1-oxo 1,2,3,4-tetrahydro-isoquinoline.
Propyl-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (.2-bromoethyl) -6-methoxy-naphthalene are prepared from (piperidyl-3) ™ and 2- (2-bromoethyl) -6-methoxy-naphthalene as in Example 1
Exit 36.8 from theoretical, so pl. 118-121 ° C.
Calculated,%: C, 74.37; H 7.25; N 5.60.
Found,%: C 74.60; H 7.43; N 5.65.
Example 19. (N- (2- (naphthyl-1) -ztil) -piperidyl-3) hydrochloride-propyl-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline.
Prepared from 2-CЈ- (p peridyl 3) propyl, 7 methylenedioxy 1 hydroxy 1,2,354-tetrahydroisoquinoline and 2 ethyl (naphtha 1) benzenesulfonic acid ester as in Example 1.
yyhod 20.8% of theoretical, so pl. 195-197 ° C.
five
0
five
0
five
0
five
0
five
Calculated,%: C 71.07; H 6.95; N 5.53; CI b, C9.
Found,%: C 71.30; H 6.95; N 5.65; C1 6.80;
Example 20. Hydrochloride (N-2 (5-methyl-6-methoxy- (naphthyl-2) ethyl) -piperidyl-2) ethyl-6,7-dimethoxy-1 oxo-1,2,3, 4-tetrahydro-isoquinoline.
Prepared from (piperidyl-2-, 7-dimethoxy-1-oxo-1, 2,3,4-tetrahydro-isoquinoline and 2- (2-bromoethyl J-5-methyl-b-methoxy-naphthalene analogously to example 1 .
Bypass 3J, 6% of the theoretical, t „ll. 95-100 ° C.
Calculated Dx 1/2 H20),%: C 68SJ8; K 7.52; N 4.98; Cl 6.30
Found,%: C 68.14; H 7.43; N 4.92; C1 6.77.
Example21. 2-j (N- (3- (naphthl 2) -oxy) propyl) -hexa-hydro-azepinyl-3) hydrochloride-methyl-6,7-dimethoxy-1-oxo-1j2s J, 4-tetrahydro isoquinoline a
Prepared from 2- (.hexahydroazepenyl-3) -methyl-6,7-dimethoxy-1-oxo-152,3,4-tetrahydro-isoquinoline and 2- (3-chloropropoxy) naphthalene, as in Example 1.
Output 16.1% of theoretical, so pl. 86-88 ° C.
Calculated (x),%: C, 66.83; H 7.42; N 5.03; Cl 6.36.
Found,%: about 66.90; H 7.40; N 5.26; Cl 6.87.
EXAMPLE 22 2 (M- (2- (5-Methyl-6-methoxy-naphthyl-2) -ethyl) hexahydro-azepinyl-3, -methyl-6,7-dimethoxy-1-oxo -1, /, 3,4-tetrahydro-isoquinoline.
Receiving: from 2- X hexahydroazepi-), 7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (2-bromoethyl) 5-methyl-6-methoxy-naphthane similar to example 1.
Exit 43, / from theoretical, so pl. 125-127 ° C.
Calculated,%: C, 74.39; H 7.80; N 5.42.
Found,%: C 74.01; H 7.82; N 5.35,
Example 23. 2- (N- (2 methyl- (naphthyl-1) -methyl; -hexahydro-azepinyl-3; -methyl-6,7-dimethoxy-1-OXO-1,2,3,4) hydrochloride -tetrahydro isoquino-lin.
Prepared from 2- (hexahydro-azepinyl-3) -methyl-6,7-dimethox-1-oxoI156182312
1,2,3,4-tetrahydro-isoquinoline and 1-Prepared from 2- (hexahydro-azepichloromethyl-2-methyl naphthalene analogues - nyl-3) methyl | 6,7-methylenedioxy-1 example 1.
. The output of 67.5% of theoretical, so pl. 128 130B
Calculated (Dx 2H20),%: C, 66.10; H 7.58; N 5.13; C1 6.5i.
Found,%: C 66.24; H 7.44; N 5.23; C1 6.85.
II p and mep 24 f 2- {Fm- (4- (naphthyl-2-hydroxy) -butyl) -hexahydro-azepinyl-3) methyl-6,7-dimethoxy-1-oxo-1,2 hydrochloride , 3,4-tetrahydro-isoquinoline.
ten
oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (2-bromoethyl) -6-methoxy-naphthalene as in example 1 of
Output 34.1% of theoretical, so pl. 147-149 ° C.
Calculated, (x),%: C 68.62, H 7.10; N 5.33; C1 6.75.
Found,%: C 68.88; H 6.98; N 5.41; C1 6.78.
PRI me R 28. Hydrochloride 2- (M- (2 (5-methyl-6-methoxy-naphthyl-2) -ethyl)
It is obtained from / - (hexahydro-azepi-15 hexahydro-azepinyl-3) -metl lb, 7nyl-3) methyl-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (4-bromo-butyloxy) -naphthalene analog is exemplary of example 1.
Yield 26% of theoretical
Calculated,%: C, 69.22; H 7.80; N 5.04; Ci 6.38o
Found,%: C 70.01; H 7.70; N 5, 5; C1 6.48 „
Example 25. Hydrochloride 2- (N- 25 (2- (naphthyl-1) ethyl) hexahydroazepinyl-3) -metsh-6,7-methylenedioxy 1-oxo-1,2,3,4-tetrahydro from oquinoline.
Prepared from 2-Ј (hexahydroazepinyl-3) methyl-6,7-methylenedioxy-1 oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (2-benzenesulfonyl-oxy-ethyl) naphthalene in a similar way Example 1. 1 Output 15.4% of theoretical, t, pl. 236-238 ° C.
Calculated U 1/2 NgO),%: C 6U, 40; H 6.82; N 5.58; C1 7.06.
Found,%: C 69.07; H 6.74; N 6.13; C1 7.29.
methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline.
Prepared from 2- (hexahydro-azepinyl-3) -methyl-6,7-methylenedioxy-1-2o-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (. 2-bromoethyl) -5- methyl 6-methoxy-naphthalene analogously to example 1,
Output 36.1% of theoretical, so pl. 112-114 ° C.
Calculated (x H20),%: C 67.07; H 7.08; N 5.04; Cl 6, J8.
Found,%: C 67.13; H 7.15; N 4, V7; C1 6.56.,
Note 29. Hydrochloride (N- (3- (, 3,4-methylenedioxy-phenoxy) -propyl) -piperidyl-3) -ethyl-6,7-dimethoxy-1-oxo-1,2,3,4- tetrahydro-isoquinoline.
Prepared from 2- (piperidyl-3) - i, 7-dimethoxy-1-ca co-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-3- (3,4-methylenedioxy-phenoxy) - propane as in example 1.
The output of 35.5% of theoretical,
thirty
35
Example 26. Hydrobromide 2- (N- 40 mp: 97-100 C. (2- (naphtch2) ethyl) -hexahydro-azepi) Calculated,%: C 59.09; H, 7.28; neur -3) -methyl -6 s 7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline „
Prepared from 2- Ј (hexahydro-azepyl-nyl-3) -methyl-6.7 methylenedioxy-1- 45 oxo-1,2,3,4-those of trahydro-isoquinoline and 2- (2-bromo-ethyl; -naphthalene analogously to the example one.
The output of 31.6% of theoretical, so pl. 100 102 ° Ci.50
Calculated,%: C 64.80; H 6.18; N 5.21; Br 14.86.
Found,%: C 65.02; H 6.07; N 5, memory; Vg.14.78.
N 4.62; C1 6.65.
Found,%: C 58.97; H 7.36; N 4.66; C1 6.52.
PRI me R 30. Hydrochloride (N- (2 (3,4-dimethoxy-phenyl) ethyl) -pyridyl-3) ethyl-6,7-dimethoxy-1-oxo-1, 2, 3,4-tetrahydro-isoquinoline.
Prepared from 2- (piperidyl-3) -ethyl 6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-bromo-2- (3,4-dimethoxy-phenyl; -ethane similar to example 1.
Output 35.9% of theoretical,
Appro. 27. Hydrochloride 2- (N-.55 mp. 103-105 C. (2- (6-methoxy-naphthyl-2) -ethyl) -hexa) Calculated,%: C 62.60; H 7 , 79; hydroazepinyl-3) -methyl-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydroisoquinoline.
N 5.21; C1 6.83o
Found,%: C 62.41; H 7.82; N 5.09; C1 7.19.
Nile-3) methyl | 6,7-methylenedioxy-1
oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (2-bromoethyl) -6-methoxy-naphthalene as in example 1 of
Output 34.1% of theoretical, so pl. 147-149 ° C.
Calculated, (x),%: C 68.62, H 7.10; N 5.33; C1 6.75.
Found,%: C 68.88; H 6.98; N 5.41; C1 6.78.
PRI me R 28. Hydrochloride 2- (M- (2 (5-methyl-6-methoxy-naphthyl-2) -ethyl) 5
methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline.
Prepared from 2- (hexahydro-azepinyl-3) -methyl-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2 - (. 2-bromoethyl) -5-methyl 6-methoxy-naphthalene analogously to example 1,
Output 36.1% of theoretical, so pl. 112-114 ° C.
Calculated (x H20),%: C 67.07; H 7.08; N 5.04; Cl 6, J8.
Found,%: C 67.13; H 7.15; N 4, V7; C1 6.56.,
Note 29. Hydrochloride (N- (3- (, 3,4-methylenedioxy-phenoxy) -propyl) -piperidyl-3) -ethyl-6,7-dimethoxy-1-oxo-1,2,3,4- tetrahydro-isoquinoline.
Prepared from 2- (piperidyl-3) - i, 7-dimethoxy-1-ca co-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-3- (3,4-methylenedioxy-phenoxy) - propane as in example 1.
The output of 35.5% of theoretical,
0
five
mp. 97-100 C. Calculated,%: C 59.09; H 7.28;
N 4.62; C1 6.65.
Found,%: C 58.97; H 7.36; N 4.66; C1 6.52.
PRI me R 30. Hydrochloride (N- (2 (3,4-dimethoxy-phenyl) -ethyl) -pyridyl-3) ethyl-6,7-dimethoxy-1-oxo-1, 2,3 , 4-tetrahydro-isoquinoline.
Prepared from 2- (piperidyl-3) -ethyl 6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-bromo-2- (3,4-dimethoxy-phenyl; -ethane similar to example 1.
Output 35.9% of theoretical,
m.p. 103-105 C. Calculated,%: C 62.60; H 7.79;
m.p. 103-105 C. Calculated,%: C 62.60; H 7.7
N 5.21; C1 6.83o
Found,%: C 62.41; H 7.82; N 5.09; C1 7.19.
Example 31. Hydrochloride (N- (2- (3,4-dimethoxy-phenyl) -ethyl) -piperidyl 3) propyl-6,7-dimethoxy 1 oxo-1,2,3 j4-tetrahydro isoquinone.
Prepared from 2- Gz- (gacheridil-3) -
- | | propyl-6,7-dimethoxy- 1 oxo 1,2,3,4 tetrahydro-isoquinoline and 1-bromo 2 (3,4-dimethoxy-phenyl) -ethane is similar to Example 1.
The output of 32.6% of theoretical, so pl, 102 106 ° C.
Calculated,%: C 63.20 | H 7.86; N 5.08; C1 b, 43 „
Found,%: C 63, memory; And 7, PP; N 4.86; Cl 6S13.
Example 32, Hydrochloride (M- (3- (3,4-methylenedioxy phenoxy) -propyl) -piperidyl-3) -proppsh3b, methoxy 1 oxo-1,2,3,4-tetrahydro- from quinoline but.
Prepared from 2- 3- (piperidyl-3) prop-6,7-dimetok si-1-oxo 1,2,3 „4 tetrahydro-isoquinoline and 1-chloro-3 (3,4-methylenedioxyphenoxy) -prolane, similarly example 1.
The output of 29.7% of theoretical, so pl.
97 100 ° C0
C, 61.63; H 7.31;
Calculated,%: 4.96; C1 6.47. Found,%: C 61.94; H 7.46;
N
5.16; Cl 6.4b.
Example 33. 2- (N (3,4-dimethoxy-benzyl) piperidyl 3) hydrochloride-methyl-6,7-dimethoxy-1-oxo-1,2,394-tetrahydro-isoquinoline
Prepared from 2 - (. Piperidl-3-methyl,) 6, 7-dimethoxy-1-oxo-1,2,3,4-tetra-hydro-isoquinoline and 3,4-dimethoxy-benzyl bromide analogously to example 1 „
The output of 53.3% of theoretical, so pl. 127-132pS
Calculated,%: C, 63.58; H 7.18; N 5.70; C1 7.220
Found,%: C 63.30; H 7.22;
N 5.52; C1 7.14.
PRI me R 34. Hydrochloride 2-G (M- (3- (4-Mec with and phenyl) -propyl) -piperidil-3,) -methyl-6, 7-dimethoxy-1-oxo - 1,2,3,4-tetrahydro-isoquinoline.
Prepared from 2 (piperndyl-3 methyl) 1 6,7-dimethoxy-1-oxo-1,2,3,4-tetra-hydro-isoquinoline and 1-bromo-3- (tox-phenyl) -propane as in Example 1 .
Output 42% of theoretical, so pl. 229-2L ° C.
Calculated by / „. C, 66.31; H 7.63; N 5.73; C1 7.25 „
ten
15
Found,%: C 66.27; H 7.64; N 5.65; C1 7.33.
PRI me R 35. Hydrochloride (H- (3- (3-methyl phenoxy) propyl) piperidyl-2) -ethyl-6,7-dimethoxy 1-oxo-1,2, J, 4-tetrahydro isoquinoline.
Prepared from (piperidyl-2) - ethyl-6,7-dimethoxy-1-oxo-11,2,3,4-tetrahydro-isoquinoline and 1-chloro-3- (3-methyl-phenoxy) -propane analogously to example 1 .
The output of 52.4% of theoretical, so pl. 142-144 ° C
- Calculated, 7.: C, 66.85; H 7.81; N 5.57; (L 7.05
Found,%: C 6b, 73; H 7.68; N 5.53; C1 6.94
PRI me R 36. 7H hydrochloride) CN- (2- (J, 4 d11 methoxy phenyl; -ethyl; - piperidyl-2; - tshH-6,7-dimethoxy-1 oxo-1,2,3, 4-tetrahydro-isoquinoline.
Get chz (pkperidil-2) -, 7-dnmethoxy-1-gokso 1 a2,3; 4 4 tetrahydro-isoquinoline and And-bromo-2 (3,4-dig-tethoxy-phenyl) -ethane analogously to example 1.
Output 47.3% of theory, so pl. 150 - 155 ° C.
Calculated,%: C 64.72; H 7 „68 $ N 5.39; CI 6.82.
Found,%: C 64.4U; H 7.83; N 5.27; From 6.90.
Litter 37. Hydrochloride (JN- (3-benzyloxy-propyl) -piperidyl- -) -ethyl-6,7-dimethoxy-1-oxo 1,2,, 39 4-heterogydro-isohich.chol on .
Prepared from 2- 2- (piperidyl-2), 7-dimethoxy-170Ccc-1,2,3 S4-tetrahydro-isoquinoline and 1-chloro-3-benzyloxy-propane as in Example 1.
Ryhod, 5b, 3% of theoretical, mp, 116-120 ° C.
Calculated,%: C, 66.85; N 5.57; C1 7.05.
Found,%: C, 66.60; C 7, N 5.25 ;; Ci 7.25.
PRI me R 38. Hydrochloride (L (4- (4-mstoxy phenyl) -bushy-piperidyl-2) -ethyl 6,7-dimethoc-1-oxo-1,2,3,4- tetrahydro-isoquinoline,
Prepared from 2-2 (. Piperidyl 2) -, 7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-bromo-4- (4-methoxy-haenyl) -butane in analogy to Example 1 .
Output 42.8 "from the theoretical, so pl. 107-1 i: ° C.
0
five
0
five
0
five
H 7.81; , 75;
ten
15
Calculated,%: C 67, .36; H 7.99; N 5.42; C1 6.86;
Found,%: C 67,16; H 8.05; N 3.35; C1 7.34.5
Example39. (N-3- (3,5-dimethoxy-phenoxy) propyl) -piperidyl-2) ethyl-6,7-dimethoxy ™ 1-oxo-1,2,3,4-tetrahydro-isoquinoline hydrochloride.
Prepared from (piperidyl 2) -, 7 dimethoxy 1 oxo-1,2,3,4-tetrahydro-iooquinoline and 17 chloro-3 (3.5 dimethoxyphenoxy) propane as in Example 1.
The output of 56.3% of theoretical 9 t. P. 127-132 C.
Calculated,%: C, 61.41; H 7.64; N 5.10; C1 6.46o
Found,%: C 61.56; H 7.65; N 5928; C1 6.89.
PRI me R 40 about Hydrochloride (N-3- (3,4-methylenedio-fenok s) -propyl) piperidyl-2) -ethyl-6,7-dimethoxy-1-oxo 1,2, 3,4-tetrahydro-isoquinoline .25
Prepared from (piperidyl-2) -, 7-dimethoxy-1-oxo 1,2,3., 4-tetra agidroisoquinoline and 1-chloro-3- (3,4-methylenedioxyphenoxy) propane analogously to example 1 .
Output 49% of theoretical, so pl. 118-120 ° C.
Calculated,%: C 63.09; H 7.00; N 5.26; C1 6.65
Found,%: C 62.90; H 7.04; N 5.46; C1 6.79.
20
thirty
35
(3,4-methylenedioxy-phenyl) -prop as in Example 1.
Output L0% of theoretical, 236 - 238 ° C.
Calculated,%: C 64.46; H 7 N 5.57; C1 7.04.
-Found,%: C 64.30; H 6.97 N 5.59; C1 7.08.
PRI me R 43. Hydrochloride (.3- (.3,4-methylenedioxy phenoxy) saw) -piperidyl-3) methyl-6,7-di-C1-oxo-1,2,3,4 -tetrahydro-nz nolina.
Prepared from 2- (cyperidic-2). , 7 dimethoxy-1-oxo 1, 2.3 tetrahydro-isoquinoline and 1-chloro (. 3,4-methylenedioxyphenoxy) -prop as in Example 1,
Yield 46.2% of theoretical t „pl. 149 153 ° C.
Calculated,%: C 60.38; H 6 N 5.21; C1 6.60.
Found,%; C 60.30; H 6.93 N 5.29; oCl 6.37.
PRI me R 44. Hydrochloride (3- (2,6-dnmethyl-phenoxy) -propyl peridyl-3) -methyl-6,7-dimethoxy oxo-1,2,3,4 tetrahydro-isoquine
Prepared from 2- (piperidyl 3, 7-dimetho si-1-oxo-1, 2.3 tetrahydro-isoquinoline and 1-chloro 6-dimethyl phenoxy) -propane analogue to example 1.
Output 55.3% of the theoretical so pl. 131-135 ° C.
Calculated, 7: С 66.85; H 7 N 5.57; C1 7.05.
Found,%: C 66.88; H 7.95
PRI me R 41. 2- (M- (3 (3,5-dimethoxy-phenoxy) propyl) -piperidyl-3) hydrochloride-methyl-6,7-dimethoxy 1-oxo-1, 2.3 , 4-tetrahydro-isoquino- 40 N 5.5.9; C1 6.85. Kca, PRI me R 45. Hydrochloride
Prepared from 2- (piperidyl-3) -me-, 7-dimethoxy, 17 OXo -1,2,3,4-tetrahydro-isoquinoline and 1-hlrr-3- (3,5-dimetsxy-phenox ") - propane ana- 45 is logical to example 1.
(4- (2,4-dichloro-phenoxy) -butyl t readyl-3) -methyl | -6,7-dimethoxy1, 2,3,4-tetrahydro-isoquinoline
Prepared from 2- (piperidyl-3) tyl-6,7-dimethoxy-1-oxo-1,2, tetrahydro-isoquinoline and 1-chloro (2,4-dichloro-phenoxy) -butane as in Example 1.
The output of 37.5% of theoretical, so pl. 98-102 ° C.
Calculated,%: C, 62.85; H 7.35; N 5.24; C1 6,630.
Found,%: C 62.81; H 7.41; N 5.10; C1 6.75.
PRI me R 42. 2- (N- (3- (3,4-methylenedioxy-phenyl) -propyl) -piperidyl-3) -methyl-6,7-dimethoxy-1-oxo-1,2 hydrochloride , 3,4-tetrahydro-isoquinoline
Prepared from 2- (piperidyl-2) -methyl-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquin-rlin and 1-chloro-3
five
five
0
0
five
(3,4-methylenedioxy-phenyl) -propane analogously to example 1.
Output L0% of theoretical, so pl. 236 - 238 ° С.
Calculated,%: C 64.46; H 7.01; N 5.57; C1 7.04.
-Found,%: C 64.30; H 6.97; N 5.59; C1 7.08.
PRI me R 43. Hydrochloride (.3- (.3,4-methylenedioxy phenoxy) propyl) -piperidyl-3) methyl-6,7-dimethoxy-1-oxo-1,2,3, 4-tetrahydro-nzoquinoline.
Prepared from 2- (cyperidic-2) me. , 7 dimethoxy-1-oxo 1, 2,3,4-tetrahydro-isoquinoline and 1-chloro-3- (.3,4-methylenedioxyphenoxy) propane as in Example 1,
Output 46.2% of theoretical, t „pl. 149 153 ° C.
Calculated,%: C 60.38; H 6.94; N 5.21; C1 6.60.
Found,%; C 60.30; H 6.93; N 5.29; OCl 6.37.
PRI me R 44. Hydrochloride 2 ™ JXN- (3- (2,6-dnmethyl-phenoxy) -propyl) -i-. peridyl-3) -methyl-6,7-dimethoxy-1-oxo-1,2,3,4 tetrahydro-isoquinoline.
Prepared from 2- (piperidyl 3) -methyl-6, 7-dimethoc-1-oxo-1, 2,3,4-tetrahydro-isoquinoline and 1-chloro-3- (2, 6-dimethyl-phenoxy) -propane similar to example 1.
The output of 55.3% of theoretical, so pl. 131-135 ° C.
Calculated, 7: С 66.85; H 7.81; N 5.57; C1 7.05.
Found,%: C 66.88; H 7.95;
N 5.5.9; C1 6.85. PRI me R 45. Hydrochloride
(4- (2,4-dichlorophenoxy) -butyl tiperidyl-3) methyl | -6,7-dimethoxy-oxo-1,2,3,4-tetrahydro-isoquinoline.
Prepared from 2- (piperidyl-3) -methyl-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-4- (2,4-dichlorophenoxy) - butane as in example 1.
The output of 54.1% of theoretical, so pl. 125 - 128 ° C.
Calculated,%: C 58.12; H 6.32; N 5.02; C1 19.06.
Found,%: C 58.21; H 6.38; N 5.08; C1 18.85.
PRI me R 46. 2- (N- (2- (3,4-dimethoxy-phenyl) ethyl) piperi-,) - methyl-6,7-dimethoxy-1-oxo-1,2, hydrochloride, hydrochloride 3,4-tetrahydro-isoquinoline.
171
Prepared from 2-Ј (piperidyl-3) -methyl 6,7-dimethoxy-1-oxo-1,2,3,4-heter. - hydro-isoquinoline and (3,4-di-methoxy-phenyl) -ethane in the same way example 1.
The output of 57.5% of theoretical, so pl. 118 - 121 ° C.
Calculated,%: C 64.2T; H 7.38; N 5.55.
Found,%: C 64E18; H 7.36; N 5.19.
PRI me R 47. Hydrochloride (N (3- (3,4-dimetho c-phenoc b)) propyl.) - piperidinyl-3; -metnl-6,7-dimethoxy-1-OXO-1,2 , 3,4-tetrahydro-isoquinoglin a.
Prepared from 2- (pieridil-3) -me-; , 7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-3- (3,4-dimethoxy-Lenoxy) propane as in Example 1.
The output of 62.5% of theoretical, so pl. 112 - 115 ° C.
Calculated,%: C 60.80; H 7.47; N 5.24.
Found,%: C 6Q, 65; H 7.69; N 5, .27.
Example 48. 2- (.N (3- (3,4 dimethoxy-phenoxy) propyl) hydrochloride.) - piperidyl-3) methyl 6,7-methylenedioxy-1-oxo-1,2,3,4 tetrahydro-isoquino lina.
Prepared from 2- (piperidyl-3) -me-, 7-mg-dialenedioxy-1 oxo-1,2,3, 4-tetrahydro-isoquinoline and 1-chloro-3- (3,4-dimethoxy-phenoxy-propane, in analogy to example one.
Yield 60% of theoretical, mp 97–100 ° C.
Calculated,%: C 60.38; H 6.94; N 5.40; Cl 6.6U.
Found .: / “: C 60.20; H 6.97; N 5.2.1; C1 6.83 /
II p and me 4U. 2- (m (2- (4-methoxy-phenyl) -ethyl) -piperidyl-3) methyl-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline hydrochloride.
Prepared from 2- (piperidyl-3) methyl-6,7-methylenedioxy-1-oxo-1,2,3, 4-tetrahydro-isoquinoline and 1-chloro-2- (4-methoxy-phenyl-ethane example 1.
Output 71.4% of theoretical, so pl. 195 - 197 ° C.
Calculated,%: C, 62.94; H.6.97; N 5.87; C1 7.73.
Found,%: C 62.90; H 6.98; N 5.68; C1 8.04.



ten
20
25
1823

thirty
35
40
45
0
five
18
PRI me R 50. Hydrochloride 2- (N- (2- (3,4-dimethoxy-phenyl.) - ethyl.) - piperidyl-3) -methyl-6,7-dimethyl-1-ocean o-1,2,3,4-tetragchdro-isoquinoline and 1-bromo-2- (3,4-dimethoxy-phenyl) -ethane as in Example 1.
The output of 41.9% of theoretical, so pl. 13Z - 134 ° C.
Calculated,%: C, 63.57; H 8.10; N 5.4U; C1 6, V5.
Found,%: C 63.70; H 8.26; N 5.45; C1 7.13.
Pr immer51 „Hydrochloride 2 (N- (3-, (4-methoxy-phenoc si) propyl) -pyridyl-3-methyl-6,7-dimethyl-1-oxo-1,2,3,4- tetrahndro isoquinoline.
Prepared from 2- (piperidyl-3) -methyl-6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloro 3 - (4-methoxy-phenoxy ) -propane analogously to example 1.
The output of 57.8% of theoretical, etc. 144-146 ° C.
Calculated,%; C 68.55; H 7.88; N 5.92; C1 7.49.
Found, 7: С 68.45; H 7.80; N 6.11; C1 7.33.
PRI me R 52. Hydrochloride 2- (N- (.3- (3-methoxy.i-phenoxy,) propyl) -piperidyl-3) -methyl-6,7-methylenedioxy-1-oxo -1,2,3,4-tetrahydro-isoquinoline.
Prepared from 2- (piperidyl-3) -methyl-6,7-methylenedioxy-1-oxo-1,2,3, 4-tetrahydro-isoquinoline and 1-chloro-3- (3-methoxy-phenoxy) -propane similar to example 1.
Output 32.5% of theoretical, so pl. 142 - Ub ° C.
Calculated,%: C 60.58; H 6.95; N 5.52; C1 6.99.
Found, Z: C 60.42; H 6.92;
N 5.50; C1 7.18.

PRI me R 53. Hydrochloride-2 (N- (3- (3-methyl-phenoxy) -propyl} -piperidyl-3) -methyl-6,7-methylenediaxy-1-oxo-1,2 , 3,4-tetrahydro-isoquinoline.
Prepared from 2-Xpiperidyl-3) -methyl-6.7 methylenedioxy-1-oxo-J, 2,3, 4-tetrahydro-isoquinoline and 3- (Tyl-phenoxy) -1-chloropropane analogously to Example 1.
The output of 31.6% of theoretical, t. Mp. 178 - 180 ° C.
Calculated,%: C 63.59; H 6.97; N 5.70; C1 7.22.
Found,%: C 63.59; H 6.92; N 5.86; C1 7.50.
Example54. 2-H N-3- (4-methoxy-1H-methyl-phenyl amino) -propyl dihydrochloride, -propyl, -piperidyl-3) -methylP 6,7-dimeth oxy-1-oxo 1, 2,3,4- tetrahydroisoquinoline.
Prepared from 2- (piperidyl-3) -methyl) -6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-3 - (. 4-methoxy-M- methyl-phenylamino) -propane analogously to example 1.
The output of 52.5% of theoretical, so pl. 180 - 183 ° C.
Calculated,%: C 60.64; H 7.45; N 7.58; C1 12.79.
Found,%: C 60.50; H 7.35; N 7.56; C1 12.87.
PRI me R 55. 2-Ј3 dihydrochloride (I - (, 3-pyridyl-4-propyl) -piperidyl-J) -propyl-6 7 dimethoxy-1-oxo 1,2,3,4- tetrahydro-isoquinoline.
Prepared from (piperidyl-3) -propyl-b, 7-dimethoxy 1-oxo-1,2,3,4-tetrahydro-isoquinoline, and 4 (3 chloropropyl) -pyridine in the same way as in 1.
Output 48% of theoretical, tp 85 - 96 ° C (amorphous.).
Calculated,%: C 57.84; H 7.73; N 7.49; C1 12.65.
Found,%: C 57.71; H 7.91; N 7.35; C1 13.04.
Example 56. Dihydrochloride monohydrate (. (B, 7 dimethoc-isoquinolyl 4) ethyl) piperidine 3) propyl 1-6,7-dimethoxy 1 oxo-1,2,3,4 tetrahydro-isoquinoline.
Prepared from (pyridyl-3) -propyl-6, 7-dimethoxy-1-oxo-1, 2,3,4-tetrahydro-isoquinoline and 4- (2-chloro-ethyl) -6,7-dimethyl-oxy- and s oh, as in example 1.
Output 34% of theoretical, so pl. 162-171 ° C (. Amorphous).
Calculated,%: C 60.17; H 7.10; N 6.57; C1 11.10.
Found,%: C 59.85; H 7.00; N 6.86; C1 11.04.
PRI me R 57. Dihydrochloride monohydrate (11- (2- (2-methyl-pyri dil-6) -ethyl) -piperidyl-3) propyl} - 7,8-dimethoxy-2-oxo- 1,3,4,5-tetrahydro-2H-3-benzazepine.
Prepared from 3-3- (piperidyl-3) -prpyl) -7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and (6-methyl-pyridyl-2) -ethyl ester of 2-benzylsulfonic acid in dimethyl
0
Q
five
five
sulfoxide with potassium carbonate at 120 ° C as in Example 1.
Yield 29% of theoretical, so pl. 105 - 113 ° C (amorphous).
Calculated,%: C 60.42; H 7.78; N 7.55.
Found,%: C 60.68; H 7.50; N 7.42.
PRI me R 58. Hydrochloride (M- (2- (6-methoxy-naphthyl 2.) ethyl,) - hyperidyl 2) -H-7,8-dimethoxy-2-oxo-1,3, 4, L-tetrahydro-2H-3-benzazepine.
Prepared from 3-Ј2- (piperidyl-2) -, 8-dimethoxy-2-oxo-19 3,4,5-tetrahydro-2H-3-benzazepine and 2 (.6-methoxy-naphthyl-2) ethyl bromide in the same way example 1.
Output 20% of theoretical, so pl. 158 - 160 ° С.
Calculated,%: C, 69.48; H 7.47; N 5.06; C1 6.41
Found,%: C 69.40; H 7.56; N 5.17; C1 6.62o
PRI me R L9. 3- - (N- (2- (5-methyl-6-methoxy-naphthyl 2) - ethyl) piperidyl-2) hydrochloride, 8-dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H -3- benzazepine.
Prepared from (piperidyl-2) -, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2 - (. 5-methyl 6-methoxy-naphthyl-2) ethyl bromide in the same way as in example one.
Bypass 28% of the theoretical, so pl. 140 - 143 ° C.
Calculated,%: C, 69.88; H 7.64; N 4.94; and 6.25.
Found,%: C 69.06; H 7.57; N 4.84; C1 6.44.
Example 60. Hydrochloride (M- (2- (naphthyl-1 oxy) -ethyl) -piperidyl-2) -ethyl-7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro 2H- 3-benzazepine.
Prepared from (piperidyl-2) -, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2- (naphthyl-1-oxy) ethyl bromide in analogy to Example 1.
The output of 27% of theoretical, so pl. 146 - 148 ° C.
Calculated,%: C 69.06; H 7.29; N 5.20; C1 6.58.
Found,%: C 69.00; H 7.07; . N 5.31; C1 6.68o
PRI me R 61. Hydrochloride (L-C2 - (. Naphthyl-1-ethyl) -piperidyl-2) -
, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro 2H-3-benzazepine.
Prepared from 3-Ј2 (liperidyl 2,) -, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H 3-benzazepine and 2 - (. Naph til-1) -ethyl bromide in analogy to example 1.
Yield 24% of theoretical, mp 148-150 ° C.
Calculated,%: C 71.18; H 7.51; N 5.36; C1 6.78.
Found,%: C 70.92; H 7.44; N 5.57; C1 7.06.
PRI me R 62. Hydrochloride-3- 2- (M- (4-naphthyl 2 oxy) -butyl.) -Piperidyl-2) ethyl J-7,8-dimethoxy-2-oxo 1, 3,4,5-tetrahydro 2H-benzazepine „
Prepared from (piperidyl 2) -ethylP - /, 8-dimethoxy 2 oxo-1j 3, tetrahydro-2H 3-benzazepine and 4- (naph tyl-2-oxy) -butyl bromide analogously to example 1.
The output of 39% of theoretical, tll 112 - 114 ° C.
Calculated,%: C 69.88; H 7.64; N 4.64; C1 6.25.
Found,% j C 69.69; H 7.53; N 4.82; C1 6.52
EXAMPLE 63, 3- L2- (N- (2- (naphthyl-2) -ethyl) -p paridyl-2) -ethyl-7,8-dimethoxy-2-oxo-1,3 hydrochloride, 4, 5-tetrahydro-2H-3-6enzazepine.
Prepared from 3- .- (. Piperidyl-2.) -7,8-dimethoxy-2 oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2 (.naphyl-2) -ethyl bromide in the same way example 1.
Yield 41% of theoretical, mp 120-122 ° C.
Calculated,%: C 71.18; H 7.51; N 5.36; C1 6.78,
Found,%: C 71.10; H 7.31; N 5.40; C1 7.05.
Example 64 Hydrochloride (N- ((2-methyl-naphthyl-1; -piperidyl-2) -, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benazepine.
Prepared from (pileridyl-2) - ethylC-7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3 benzazepine and 1-chloro methyl-2-methyl-nai) talin as in Example 1 .
Yield 24% of theory, mp 144-146 ° C.
Calculated,%: C 71.18; H 7.51; N 5.36; C1 6.78.
Found,%: C 70.93; H /, 38; N 5.48; C1 6,890
five
0
0
five
0
five
0
five
PRI me R 65. 3- (N- (2- (naphthyl-2) -ethyl) hexahydro-ase-pn-3-yl) -methyl-7,8-dimethoxy-2-oxo-hydrochloride -1,3,4,5-tetrahydro-2H-3-benzazepine.
Prepared from 3- (hexahydro-azepin-3-yl) methyl-7,8-dimethoxy-2-oxo-1, 3,4,5 tetrahydro-2H-3-benzazepine and 2- (naphthyl-2) ethyl bromide similarly example 1.
Output 58% of theoretical, so pl. 204 - 205 ° С.
C, 71.18; H 7.52;
N
7.10;
Calculated% 5.36; C1 6.78.
Found,%; C, 71.41; H 7.51; N 5.35; C1 6.50o
PRI me R 66. Hydrochloride (, N- (2- (naphthyl-2) -ethyl) -piperidyl-3) -me-, 8-dimethoxy-2-oxo-1,3E4,5-tetrahydro-2H -3-benzazepine.
Prepared from 3-Ј (piperidyl-3) -methyl-7.8 dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2- (naph-5-tyl-2) ethyl bromide in the same way example 1.
The output 35X from theoretical, so pl, 239 - 240 ° C.
Calculated,%: C, 70.78; H 7.33; N 5.50; C1 6.96.
Found,%: (J 70.70; H M 5.46; C1 7.16.
PRI me R 67. ((Naphthyl-2J methyl) -piperidyl-3) -methyl | -7,8-dime
.one
toxi-2-oxo-1,3,4,5-tetrahydro-2H-3-, benzazepine.
Prepared from 3- (piperidyl-3) -me-, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2-bromomethyl-naphthalene analogously to example 1.
The output of 27% of theoretical, so pl. 176 - 177 ° C.
Calculated,%: C 75.95; H 7.47; N 6, M
Found,%: C 76.11; H 7S28; N 6.10.
Example 68. Hydrochloride 3- Ј (N- (4-naphthyl yl-2-oxi-butyl) -piperidyl-3) methyl-7,8-dimethoxy-2-oxo-1,3,4, 5-tetrahydro -2H-3-benzazepine.
Prepared from 3 {(piperidyl-3) -me-g, 8-dimethoxy-2 oxo-1,3,4,5 -...-tetrahydro-2H-3-benzazepine and 4- (naphthyl-2-hydroxy) - butyl bromide as in example 1.
The output of 24% of theoretical, so pl. 196 - 197 ° C.
Calculated,%: C 69.48} H, 7.47;% N, 5.06; C1 6.41 „
Found,%: C 69.30; H 7.36; N 4.99; C1 6.56.
Example 69. Hydrochloride 3 (M- (4- (naphthyl 1) -ethyl) -piperidyl-3) -me-, 8-dimethoxy-2 oxo-1,3,4,5-tetrahydro-2H -3-benzazepine.
Prepared from 3- (piperidyl 3) -methyl-7.8 dimethoxy 2-oxo-1,3,4,5-tetrahydro 2H-3-benzazepine and 2- (. Naphthyl-1) -tilbromic in the same manner as in Example 1.
Output 18% of theoretical, t.mi. 230 - 231 ° C.
Calculated,%: C, 70.78; H 7S33; N 5.50; C1 6,960
Found%: (J 7Q, 71; H 7.07; N 5.67; C1 6.99,
Example 70. 3- | T (N- (2- (naphthyl-1-hydroxy) ethyl) -piperidyl 3) -methyl-7 hydrochloride; 8-dimethoxy-2 oxo-1, 3, 4,5-tetrahydro 2H -3-benzazepine.
Prepared from 3- (piperidyl 3) -methyl-7,8-dimethoxy-2 oxo-1,3,4,5-tetrahydro-2H-3 benzazepine and 2 (naphthyl-1-oxy) ethyl bromide analogously to the example one.
Output 40% of theoretical, so pl. 214 - 215 ° C.
Calculated,%: C 68.62; H 7.10; N 5.34; C1 6.75.
Found,%: C 68.40; H 7.10; N 5.21; .C1 6.77.
EXAMPLE 71: 3- ((2-methyl-naphthyl-1) -methyl) -piperidyl-3) -methyl 7 s 8-dimethoxy-2 oxo-1, 3.4, 5-tetrahydro hydrochloride 2H-3 benzene zepin.
Receiving from 3- (piperidyl-3) -methyl-7,8-dimethoxy-2-OXO-1,3,4,5-tetrahydro-2H-3 benzazepine and 1-chloromethyl-2 methyl naphthalene analogously to the example one.
Yield 67% of theory, i.e. 242 - 243 ° C.
Calculated, 7.1 ° C 70.78; H 7.33; N 5.50; C1 6E96 /
iso,%: C 70,50; H 7.22; N 5.34; C1 6.89.
Example 72. J-Ј (N- (2- (6-methoxy-naphthyl-2) -ethyl) -piperidyl-3) hydrochloride, methyl-7,8-dimethoxy-2-oxo-1,3, 4,5-tetrahydro-2H-3-benzazepine.
Prepared from 3- (piperidyl-3) -methyl-, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2- (b-methoxy-naphthyl-2) ethyl bromide similar to example 1.
Output 50% of theoretical, so pl. 156 - 157 ° С.
Calculated,%: C, 74.07; H 7.62; N 5.57.
Found,%: C 73.90; H 7.55; N 5.64.
PRI me R 73. 3- (N- (2- (5-methyl-6-methoxy-naphth-2-yl) -ethyl) -piperidyl-3) -methyl-, 8-dimer hydrochloride; toxi-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine.
Prepared from 3- (piperidyl-3) -me-, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3 benzazepine and 2- (5-methyl-6 methoxy-naphth-2- silt,) ethyl bromide analogously to example 1.
Output 53% of theoretical, so pl. 240 - 241 ° C.
Calculated,%: C, 69.48; .H, 7.47; m 5.06; C1 6.41,
Found X: C 69.58; H 7.48; N 5.00; C1 6.54.
PRI me R 74. 2-Ј (N- (2- (3,4-dimethoxy-phenyl) ethyl) hydroxychloride-1-pyridyl-3-methyl-5,6-dimethoxy-1-oxo-hydrochloride 1,3-dihydro-isoindole.
Prepared from 2-piperidyl-3) -methyl-5,6-dimethoxy-1,3-dihydro-isoinol and 2- (3,4-dimethoxy-phenyl) ethyl bromide in the same way as in Example 1. 68% of theoretical, t .pl. 225 - 226 ° C.
Calculated,%: C 63.60; H 7.18; N 5.20; C1 7.22.
Found,%: С 33.61; H 7.30; N 5.70; C1 7.44e
PRI me R 75. 2- (N- (2- (6-methoxy-naphthyl-2-ethyl piperidyl-3) hydrochloride) methyl - 5,6-dimethoxy-1-oxo-1,3-hydrochloride dihydro-isoindole.
Prepared from 2- (piperidyl-3) -me-, 6-dimethoxy-1 oxo-1,3-dihydro-isoindole and 2 (b-methoxy-naphthyl-2) ethyl bromide, as in Example 1.
Output 75% of theoretical, so pl.
234 - 236 ° C.
Calculated,%: C 68.16; H 6.90; N 5.48; C1 6.94.
Found,%: C 68.10; H 7.10; N 5.39; C1 7.10.
PRI me R 76. (2- (Naphthyl-1-hydroxy) -ethyl) -piperidyl-3) methyl-5-dimethoxy-1-oxo-1,3-dihydro-isoindole hydrochloride.
Prepared from 2- (piperidyl-3) -me-, 6-dimethoxy-1-oxo-1,3 dihydro-isoindole and 2 (naphthyl-1-oxy) - ethyl bromide analogously to example 1,
Output 60% of theoretical, so pl. 150 - 152 ° C.
Calculated,%: C 67.66; H 6.69; N 5.63; C1 7.13.
Found,%: C 67.50; H 6.76; N 5.74; C1 7.54 „
Example 77 „2- {FM- (2- (4-Methylphenyl) -ethyl) -piperidyl-3) -methyl 5, b-dimethoxy 1 oxo-1, 3-dihydro-isoindol.
Prepared from 2-Ј (piperidyl-3) me-, b dimethoxy 1-oxo-isoindole and 2- (4-methyl-phenyl) -ethyl bromide analogously to example 1.
Output 57% of theoretical, so pl. 134 - 13b ° С ..
Calculated,%: C 73.50j H N 6.86.
Found,%: C 73.40; H 8.04; N 7.06 „
Example 78, 2-G {Mn.- (2- (3-labels, si-phenyl) -ethyl) -piperidil-3,) methyl-5,6-dimethoxy-1-ox-1,3-dihydrochloride hydrochloride isoindole.
Prepared from 2- (piperidyl-3-me-, 6-dimethoxy-1-oxo-isoindole and 2 - (, 3-methoxy-phenyl) -ethyl bromide analogously to example 1.
Output 54% of theoretical, t „pl. 226 - 228 ° С „
Calculated,%; C 65.28; H 7.01; N 6.09; C1 7.71.
Found,%: C 65.30 j H, 7.37; N 5.91; C1 7.61.
Example 79. 2- (.N- (2 - (. 5-methyl-6-methoxy-naphthyl) 2) ethyl) piperidyl-3 hydrochloride.) - metihG {5,6-dimethoxy-1-oxo-1,3- dihydro-isoindole.
Prepared from 2-G (piperidyl-3) -methylT-5,6-dimethoxy 1-oxo 1,3-dihydro-isoindole and 2- (5-methyl-6-methoxy-naphthyl-2) ethyl bromide similar to example 1.
Exit 38% of theoretical, so pl.
214- 216 ° C.
Calculated, U: C 68.62; H 7.10; N 5.33; C1 6.75,
Found,%: C 68.94; H 7.23; N 4.98; C1 6.61
Example 80 2- (N- (2- (4-nitrophenyl) ethyl ethylpiperidyl) hydrochloride
3) -methyl 5,6-dimethox-1-oxo 1,3 dihydro-from oindole.
Prepared from 2- (. Piperidyl-3) -me-, 6-dimethoxy-1-oxo-1,3-dihydro-isoindole and 2- (4-nigrophenyl) -
ethyl bromide as in example 1.
Output 79% of theoretical, so pl.
215-218 ° C.
Calculated,%: C 60.56; H 6.35; . N 8.83; C1 7.45.
Found 7; C 60.41; H 6.26; N “, 84; C1 7.62.
Example 81. 3- (CH # (2- (thienyl-2) -ethyl) -piperidyl-3) -methyl-7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H- hydrochloride 3-benzazepine.
Prepared from 3- (piperidyl-3) -methyl 1-7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro 2H-3-benzazepine and 2- (2-bromoethyl) -thiophene analogously to the example one.
 -Exit 43% of theoretical, tpl 232 - 236 ° C.
Calculated,%; C 61 „99; And 7.15; N 6.02; C1 7.62; S 6.89.
Found,%: C 61.90; H 7.06; N 5.78; C1 7.96; S 6.84.
PRI me R 82. 3- (N (2- (thienyl 3) -ethyl) piperidyl-3-methyl-8-dimetok-2 oxo-1,3,4,5-tetrahydro-2H 3 benzazepine hydrochloride,
Prepared from 3- (Xpiperidyl-3) -methyl 3-7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-bazazepine and 3- (2-bromoethyl) -thiophene ana .pogic example 1.
Output 36% of theoretical, sintering at 75 - 80 С, melting at 225 - 230 ° С „
Calculated,%: C 61S99; H 7.15; N 6.02; C1 7.62; S 6.8U.
Found 2 L 62.00; H 7.08; N 5.98; C1 8.43; S 6.62.
Example of 3-Ј (N (. 4- (. Thienyl-2) -butyl) -piperidyl-3) hydrochloride - me-, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3 is benzazepic.
Prepared from 3-Hpiperidyl-3) -methyl-7,8-dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H 3 benzazepine and 2- (4 bromobutyl) -thiophene analogously to example 1.
Yield 68% of theoretical, mp 190-196 ° C.
Calculated,%: C 63.33; H 7.56; N 5.68; C1 7.19; S 6.50.
Found,%: C 63.18; H 7.72; N 5.72; C1 7.29; S 6.59.
PRI me R 84. (2- (Benzo) H | furyl 2) -ethyl) -piperidyl-3) methyl 3 7 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro hydrochloride -2H-3-benzazepine,
Prepared from 3- (pilerydil-3). thyl) -7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H 3 benzazepine and 2- (2bromoethyl) -benzo | b-furan, similarly
example 1.
Yield 22% of theoretical, mp above 216 ° C (decomposition).
Calculated,%: C H 7.07;
N 5, s.
Found,%: C 67.14; H 7.36; N 5.53. .
Example 85. 3-JXN- (2-benzo VJ thienyl-3)) - piperidyl 3) -methyl-7.8 dimethoxy-2 oxo-1,3,4, 5-tetrahydro 2H 3-benzazepine hydrochloride.
Prepared from 3-Xpiperndyl-3) -methyl-7,8-dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 3 - (. 2-bromoethyl) benzo-thiophene analogously to example 1
Output 73% of theoretical, tnl. 70 - 75 ° C (decomposition).
Calculated,%: C, 65.29; H 6.85; N 5.44.
Found,%: C 65.10; H 6.87; N 5.73.
PRI me R 86. 3-Ј (n (, 2- (4-methoxy-benzo b, thienyl-3) ethyl-piperidyl-3) -methyl-7,8-dime-to-2-oxo hydrochloride 1,3,4,5-tetrahydro 2n 3-benzazepine.
Prepared from 3- Ј (piperidyl 3) -methyl-7,8-dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 3- (2-chloroethyl) -4-methoxy-benzo bj thiophene as in example 1.
Yield 25% of theory, mp, 85 - 105 ° C (decomposition).
Calculated,%: C, 63.96; H 6.84; N 5.14; Cl b, 50; S 5.88.
Found% "C 63.95; H 6.85; N 4.99; C1 6.53; S 5.75.
Example 87. 3- (N- (6-methylsulfonyloxy- (benzo) thienyl-3) ethyl) -piperidyl-3) hydrochloride 7.8-dimethoxy 2-oxo-1,3,4, 5 tetrahydro 2H-3-benzazepine.
, Obtained from -3-Hpiperidyl 3) me-, 8-dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 3,2- (methylsulfonyloxy) ethyl 6 methylsulfonyloxy-benzo JV thiophene analogously to example 1.
Yield 55% of theoretical, tpl 90 ° C (decomposition).
Calculated,%: C 37.18; H 6.12; N 4.60; C1 5.82; S 10,53.
Found,%: C 57.25; H 6.14; N 4.50; C1 5.97; S 10.36.
PRI me R 88. Hydrochloride 3 - {Xy- (5- (thienyl-2) -pentyl) -piperidyl-3) -methyl 7,8-dimethoxy-2-oxo-1,3,
4,5-tetrahydro-2H-.3-benz azepine,
Prepared from 3- (piperidyl-3) -methyl-, 8-dimetok si-2-oxo-1, 3,4,5-tetrahydro-2H-3-benzazepine and 2-1.5-methylsulfonyloxypentyl) -thiophene by analogy with example 1.
Output 39% of theoretical, tp 177 ° С „
Calculated,%: C, 63.95; H 7.75 | N 5.52; C1 6.99; S 6.32.
Found,%: C 63.70; H 7.92; N 5.40; C1 7.24; S b, 62.
PRI me R 89. Hydrochloroyl, 3- | (H- (2- (furyl-2) ethyl) -piperidyl-3) methyl-7,8-dimethoxy 2-oxo-1,3,4, 5tetrahydro-2H 3-benzazepine.
Prepared from 3- (piperidyl-3) -methyl-7.8 dimethoxy 2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2- (2-methyl lionyloxyethyl) furan as in Example 1.
Output 44% of theoretical, tpl 205 - 215 ° C.
Calculated,%: C 64.20; H 7.41 | N 6.24; C1 7.90.
Found%: C 64.00; H 7.45; N 6.00; C1 7.80.
PRI me R 90. 3- (H- (3- (furyl-2) -propyl) -piperidyl-3) -methyl-, 8-dimethoxy-2-oxo-1,3, 4,5- hydrochloride hydrochloride tetrahydro-2H-3-benzazepine.
Prepared from 3-Hliperidyl-3) -methyl-7,8-dsh "1-methoxy-2-oxo-1, 3,4,5-tetrahydro-2H-3-benzazepine and 3- (furyl-2) -propionic aldehyde as in example 4.
Output 11% of theoretical, tp 201 - 206 ° C.
Calculated,%: C, 64.85; H 7.62; N 6.05; C1 7.66.
Found,%: C 64.88; H 7.76; N 5.93; C1 7.55.
 Example 91. 3- Ј (N- (6-1thienyl-2) -hexyl) -piperidyl 3) -7.8-dimethoxy-2-oxo 1,3, 455-tetrahydro-2H-3-benzazepine hydrochloride.
Prepared from 3- (piperidyl-3) -methyl-7, 8-dimetok sy 2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 2- (6-methylsulfonyloxyhexyl) -thiophene analogously to example 1 .
Output 27% of theoretical, mp 160 ° С „
Calculated / 5: C, 64.39; H 8, GO; N 5.40; C1 6.79.
Found,%: C 64.55; H 7.90; N 5.23; C1 7.00.
29
PRI me R 92. Hydrochloride-3- (N- (3- (indolyl-3) -propyl) -piperidyl-3) methyl-7,8-dimethoxy-2-oxo-1,3, 4,5 tetrahydro-2H-3-benzazepine. Prepared from 3- (piperidyl 3) -me, 8-dimethoxy 2-oxo-1,3,4,5 tetrahydro-2H-3-benzazepine and 3- (3-methylsulfonyloxypropyl) -indole in analogy with example 1.
Yield 19% of theoretical, t.p. 80 ° C (decomposition).
Calculated,%: C 60.42; H 6.30; N 6.45.
Found,%: C 60,32; H 6.47; N 6.67.
PRI me R 93. Hydrochloride 3- Ј (H- (2-g (indolyl-3) -ethyl) -piperidyl) methyl-7.8 dimethoxy-2-oxo-1,3,4,5 - tetrahydro-2H-3-benzazepine.
Prepared from 2-(piperidyl-3) -me-, 8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 3- (2-methylsulfonyloxyethyl) indole as in Example 1 .
Yield 23% of theoretical, tp 80 ° C (decomposition).
Calculated, 7: С 65.53; H 6.42; N 7.69.
Found,%: C 65.33; H 6.55; N 7.80.
PRI me R 94. Dihydrochloride-3-L7- (3- (4 methoxy-M-methyl phenylamino-propyl) -piperid-Ztil) -methyl-7,8-methylenedioxy-2-oxo-1,3, 4,5-tetrahydro-2H-3-benzazepine.
Prepared from 3- (piperidyl-3-methyl) 7,8-methylenedioxy-2-oxo-1, J, 4,5-tet rahydro-2H-3-benzazepine and 1-chloro-3- (4-methoxy-no. - methyl-phenylamino) -prop in analogy to example 1.
The output of 24.2% of theoretical, so pl. 219 - 221 ° C.
Calculated,%: C 58.94; H 7.25; N 7.61.
Found,%: C 59.08; H 7.45; N 7.75.
Example 95: 2- (N- (3- (6-methoxy-naphthyl-2-hydroxy) propyl) -azacyclo-3-3) methyl-6.7 dimethoxy-1-oxo-hydrochloride 1,2,3,4-tetrahydroisoquinoline.
Prepared from 2- (azacyclooctyl-3) -methyl-6,7-dimethoxy-1-oxo-1,2,3,4 tetrahydro-isoquinoline and 2- (3-chloropropoxy) -6-methoxy-naphthalene analogously to example 1 „
The output of 24.4% of theoretical, so pl. 176 - 178 ° С „
ten
15
20
25
.

h
.
) 35
- - - 40
- -
30 C 67.96; H 7.43;
thirty
45
50
55
Calculated,% N 4.80; C1 6.08;
Found,%: C 67.74; H 7.29; N 4.71; C1 6.23.
PRI me R 96. Hydrochloride 3- Ј (L- (3- (indolyl-3) -pyrrolidyl 3) -me-, 8-dimethyl-2-oxo-1,3,4,5-tetrahydro 2H-3-benzazepine.
Derived from 3- (pyrrolidyl-3) -methyl-7,8-dimethyl-2-oxo-1,2,3,4-tet4-rahydro-2E-3-benzazepine and 3- (3-ben-, zolsulfonyloxy- propyl) -indole as in example 1.
. Output 62% of the theoretical, mp, 106 - 108 ° C.
Calculated,%: C 69.47; H 7.91; N 8.68; C1 7.32.
Found,%: C 69.57; H 7.80; N 8.67; C1 8.51.
Take R-97. 3- (P- (3- (6-methoxy-naphthyl-2-oxy) -propyl) -hexahydroazepine-3) methyl -1, 2,3,4-tetrahydro-2-oxo- 2H-3-benzazepine.
Prepared from 3- (hexahydro-azepi-nyl-3) metip -1,2,3,4-tetrahydro-2-oxo 2H 5-benzazepine and 2- (3-chloropropoxy) -6-methoxy-nzphthalene similar to example 1.
Output 45% of theoretical, so pl. 109 - 111ES.
Calculated,%: C 72.50; H 7.74; N 5.12.
Found,%: C 72.35; H 7.68; N 4.93.
Example 98. 3- (N- (3- (b-methoxy-naphthyl 2-hydroxy) propyl) -hexagicro azepinyl-3) hydrochloride 1, J, 4, 5-tetrahydro-7,8-methylenedioxy-2- oxo-2H-3-benzazepine.
Prepared from 3- (hexahydro-azepi-nyl-3) -methyl -1, 3,4,5-tetrahydro-7,8-methylenedioxy-2-oxo-2H-3-benzazepine and 2- (3-chloropropoxy) -6-methoxy-naphthalene analogously to example 1.
The output of 68.1% of theoretical, so pl. 104 - 10 ° C.
Calculated (x 2H20),%: C 65.46; H 7.38; N 4.79; Cl b, 06.
Found,%: C 65.60; H 7.25; N 5.01; C1 6.43.
Example 99. 2- (No. (3- (6-methoxy-naphthyl-2-hydroxy) -propyl) -hexahydro-azepinyl-3) hydrochloride methyl 6,7-methylenedioxy-1-oxo-1,2,3 , 4-tetra-hydro-isoquinoline.
Prepared from L-Ј (hexahydro-azei-enyl-3) -methyl-6,7-methylenedioxy-1-ox-so-1,2,3,4-tetrahydro-isoquinoline and
2- (3-chloropropox) -6-methoxy naphthalene as in example 1.
Output 18.2% of theoretical, so pl. 65 - 67 ° С, 5
Calculated (x H20),% C 65.19; H 6, d8; N 4.90} C1 6.20.
Found,%: C 65.2Q; H 6.75; N 4.82; C1 6.54.
Example 100. 2-JQ 4N- (3- (.b-methoxy-naphthyl-2-hydroxy) -propyl) -hexahydro-azepinyl-3) hydromethyl, 7-dimethyl-1 oxo-1,2,3 hydrochloride , 4-tetrahydro-isoquinoline.
Prepared from 2-Xhexahydro-azepi-15-nyl-3) -methyl-6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 2- (3-chloro-propoxy) 6-methoxy- naphthalene analogously to example 1. Output 17.3% of theoretical, 20 so pl. 68 - 73 ° C.
Calculated, (x 2H40),%: C 67.06; H 7.93; N 4.46; C1 6.66.
Found 7.: C 67.05; H 7.73; N 4.88; C1 6,
Example 101 3- (N- (3-45,6-Dimethoxy-naphthyl-2-hydroxy) -propyl hexahydroazepinyl-3) methyl -1,3,4,5-tetrahydro-7,8-dimethoxy-2- OXO-2H-3-benzazepine .30
Prepared from (hexahyd. Ro-azepinyl-3} -methylP-1,3,4,5-tetrahydro-7,8-dimethoxy 2-oxo-2H ° -3 benazepine and 2- (3 chlorpropoxy) -5, 6-dimethoxy-naphthalene analogously to example 1. $$
The output of 52.4% of theoretical, so pl. 129 - 131 ° C.
Calculated,%: C, 70.81; H 7.69; N 4.86.
Found,%: C 70.66; H 7.84; 40
N 4.63.
Example 02 j 3- / JJIN- (3- (5,6-dimethoxy-naphthyl-2-hydroxy) -propyl) hydrochloride) hexahydro-aepeninyl-3) methyl-1,3,4,5-tetrahydro hydrochloride 7,8-dimethyl- 45 2 oxo-2H-3-benzazepine.
Prepared from 3- (hexahydro-azepinyl-3) -methyl -1,3,4,5-tetrahydro-7,8-dimethyl 2-oxo-2H-3-benzazepine and 2- (3-chloro-propoxy) 5,6-dimethoxy-naphtha 50-talin in analogy to example 2.
Output 47.5% of theoretical, so pl. 90-966С.
Calculated (x HgO),%: C 68.15; H 7.90; N 4.67; S1 5,9GG55
Found,%: C 67.93; H 6.94; N 5.05; C1 6.09.
Example 103. 2- N- (3- (5,6-dimethoxy-naphth-2-hydroxy) -propyl) -piperidyl-3, -Hydrochloride-1-oxo-1,2-hydrochloride, 3,4-tetrahydroisoquinoline.
Prepared from 2- (piperidyl-3) IU, 7-methylenedioxy 1-oxo-1,2,3, 4-tetrahydro-isoquinoline and 2- (3-chloro-propoxy) -5,6-dimethoxy-naphthalene analogously to example 1.
The output of 22.5% of theoretical, so pl. 93 - 98 ° C.
Calculated (x),%: C 63.42; H 6.69; N 4.77; C1 6.03.
Found,%: C 63.59; H 6.80; N 4.70; C1 6.28.
Example 104. 2-G (N- (3- (5,6-dimethoxy naphthyl-2-hydroxy) propyl) -pyrrolidyl-3) hydrochloride-methyl-6,7-methylenedioxy-1-bess-1,2,3 , 4-tetra-hydroisoquinoline.
Prepared from 2-pyrrolidyl-3) -methystine | -6,7-methylenedio si-1-oxo-1,2,3, 4-tetrahydro-isoquinone and 2- (3-chloropropoxy) -5,6- dimethoxy-naphthalene analogously to example 1.
The output of 22.5% of theoretical, so pl. 87 - 90 ° C.
Calculated (x H2O ;,%: C, 62.87; H, 6.50; N, 4.88; C1, 6.18.
Found,%: C 62.72; H 6.38; N 4.93; C1 6.30.
Example 105. 2-XN- (3- (5,6-dimethoxy-naphthyl-2-hydroxy) propyl) -piperidyl-3) methyl-6,7-dime-1-ok co-1,2,3 hydrochloride , 4-te of agidro-isoquinoline.
. Obtained from 2- (piperidyl-3) -methyl-6, 7-dimethyl-1-oxo-1, 2,3,4-tetrahydro-isoquinoline and 2- (3-chloropropoxy} -5,6-dimethoxy -naphthalene as in example 1.
The output of 21.3% of theoretical, so pl. 72 - 78 ° C.
Calculated (x H20),%: C 67.30; H 7.59; N 4.90; C1 6.21.
Found,%: C 67.44; H 7.74; N 5.06; C1 6.53.
Example 106. 2- Ј (, N- (3- (5,6-dimethoxy-naphthyl-2-hydroxy) propyl-hexahydro-azepinyl-3) -methyl-6,7-dimethyl-1-oxo-1 hydrochloride, 2,3,4-tetrahydro-isoquinoline.
Prepared from 2-Ј (hexahydro-azepinyl-3) -methyl-6,7-dimethyl-1-ocean-1,2,3,4-tetrahydro-isoquinoline and 2-. (3-chloropropoxy) -5,6-dimethoxy-naphthalene analogously to example 1.
Output 12% of theoretical, tp 84 - 90 ° C.
Calculated (x),%: C 67.73; H 7.73; N 4.78; Cl b, 06.
Found,%: C 67.64; H 7.81; N 4.94; C1 6.20.
Example 107. 2- (N- (3- (Indolyl-3) propyl) piperidyl 3) -methyl 5,6-dimethoxy-1-OXO-1,3-dihydro-isoindole x 1.3 benzenesulfate trigndrate .
Prepared from 2-jCHpiperidine 3.) -Methyl 5,6-dimethoxy-1-oxo-1, 3-dihydro-iso-indole and 3- (3-benzenesulfonyloxy-propyl) -indole in dimethylformamide and triethylamine analogously to Example 1.
Output 45% of theoretical, tp 87 - 89 ° C.
Calculated,%: C 58.51; H 6S54; N 5.68.
Found,%: C 58.66; H 6.43; N 5.34.
Example 108. Benzene sulphonate 2- (M- (3-indolyl-3) -propyl piperidyl-3) -methyl-6,7-dimethyl-oxo-1j2,3,4-tetrahydro-isoquinolic dihydrate.
 Prepared from 2- Hpiperidyl-3) -methyl-6,7-dimethyl 1-oxo-1 s 2,3,4 ™ tetrahydro-isoquinoline and 3- (3 Beisol sulfonyloxy-PrO-indole in dime-
tilformamide and triethylamine analogue- 30 Ram can be obtained the following
but example 10
Output 94 from the theoretical, m.p. 117 - 119 ° C.
Calculated,%: C, 65.46; H 7.27; N 6.73.
Found,%: C 65.51; H 6.91; N 6.72.
Example 109. 3- Ј (M- (3- (indolyl-3) -propyl) -hexahydro-azepini, p-3) -methyl-7,8-dimethoxy-2-oxo-1,3,4 monohydrate , 5-tetrahydro-2H-3-benzazepine.
Prepared from 3 - {(hexahydroazepenyl-3) -methyl1-7,8 ™ dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 3- (3-benzenesulfonyl-oxy propyl) indole in dimethylformamide and triethyl-amine as in example 1.
Output 49% of theoretical, so pl. 56 - 58 ° C.
Calculated, 7, C 70.98; H 8.14; N 8.27.
Found,%: C 71.08; H 8.10; N 8.16.
Example 110. -3-N-3- (indolyl-3) -propyl monohydrate-o-azepinyl-3) hexahyd-7,8-methylenedioxy 2-oxo-1,3,4,5-tetrahydro-2H- 3-benzazepine.
0
five
Prepared from 3- (hexahydro-azepinyl-3) -methyl-, 8-methylenedioxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and 3- (3-benzenesulfonyloxy) propyl) -indole as in example 1.
The output of 61.5% of theoretical, so pl. 62 -, 64 ° C.
Calculated,%: C, 70.84; H 7.59; N 8.55.
Found,%: G 70.73; H 7.59; N 8.42.
Example 111 2-G (H- (3- (cndolyl-3) -propyl) -pyrrol-5-di-3) -methyl-6,7-dimethyl-1-oxo-1,2s3s-Tecpari-iflpo-isoquinoline hydrochloride x 1.5 hydrate.
Prepared from 2- (pyrrolidyl-3) -methyl-7,8-dime-1-oxo-1,2,3,4-tetrahydro-isoquineline and 3- (3-benzene-sulfonyloxy-propyl) -indole similar to example 1.
Yield, 67% of theoretical, so pl. 117 - 120 ° C.
Calculated,%: C 67.69; H 7.78; N 8.77; C1 7.40.
Found,%: C 67562; H 7.80; N 8.72; C1 7.93.
Similar to the above example
five
0
five
0
compounds.
Hydrochloride 2-M- (3- (naphthyl-2-hydroxy) -propyl) -piperidyl-3) methyl-6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro hydrate isoquinoline, so pl. 152 - 154 ° С.
Calculated,%: C, 70.50; H 7.69; N 5.495 C1 6.93.
Found,%: C 70.31; H 7.52; N 5.49; C1 75yu.
Dihydoochlornd 2- (K- (3- (naphthyl-2) -propyl) -piperidyl-3) -methyl-6,7-dimethyl-1,2,3,4-tetrahydro-yloquinoline, m.p. 148 - 150 ° C.
Calculated,%: C 69.61; H 8.18; N 5.41; C1 13.70.
Found,%: C 69.46; H 8.32; N 5.26; C1 14.17.
2- (M- (3- (pyridyl 3) -propyl) -liperidyl-3) methyl-5,6-methylenedioxy-1-oxo-1,3-dihydro-iso-indole dihydrochloride, m.p. 165 to 167 ° C.
Calculated,%: C 59.22; H 6.27; N 9.00; C1 15.20.
Found, C 59.03; H 6.45; N 8.85; C1 15.06.
3- Ј (K (- (3- (pyridyl-3) -propyl) -pyrrolidyl-3) methyl 335156182336 dihydrochloride
7.8 dimethoxy-2-oxo-1 „3,4,5-tetramethyl-1-oxo-1, 2,3,4-tetrahydro-iso-hydro 2H-3-benz oazepine, m.p. 96 - quinoline, t „pl. 185 - 187 ° C. 98вС. 4 Calculated,%: C 75.52; H 7.82;
 Calculated,%: C 60.42; H 7.11; N = 5.87; C1 7.43. N 8.46; C1 14.28; Found,%: C 75.39; H 7.85;
Found, Z: C 60.35; H 7.46j N 5.82; Cl 7.52. N 8.43; C1 14,58. Dihydrochloride-2 (No.- (3 - (naphthyl-2 Dihydrochloride 2 (No.- (3- (H-ethyl-oxi) -propyl) piperidyl 3,) - methyl 3, 4-dimethyl-anilino ) -propyl) -piperi JQ 6.7 dimethyl-1,2,3,4-tetrahydro-iso-dyl-3) methyl 1 6.7 dimethoxy 1-oxoquinoline, m.p. 133 - 135 ° C. 1,2,3,4-tetrahydro-isoquinoline, so pl. Calculated U),%: C 68.30; 97 - 100ffC. H 6.87; N 5.31; C1 13.44;
Calculated,%: C, 61.63; H 8810 | Found,% ;. c 68.05; H 6.85;
N 7.18; Cl 12.12: I5 N, 5.23; Cl 13.03.
Found,% 2 C 61.52; H 8.15; Dihydrochloride 2-W- (3- (naphthyl-2
N 6.92; Cl 11.82, oxy) -propsh1; piperidyl-3) -metshG Dihydrochloride 2- (N- (3- (3-methyl-6 97-methylenedioxy-1,2,3,4-tetrahydrophenoxy) propyl) -piperidyl-3) -meso-quinoline, m.p. 130-132 ° C.
, 7-dimethoxy 1,2,3 (4 tetrahydrin-20 Calculated. U),%; C63.62; ro-isoquinoline, so pl. 100 - 103 ° C; H 6.62; N 5.11; C1 12.95.
Calculated, X: C, 61.23; H 7.99; Found,%: C 63.49; n 6.86; N.5.29; C1 13,39.N Cl 12.64.
Found,%: C 61.21; H 8.13; Dihydrochloride 2- (H- (2-methyl- (naphN 5,10; C1 13.15 s, 25 tyl-1) methyl; piperidyl-3) methyl Hydrochloride 2 (No.- (3- (naphthyl-2 o1c- 6.7 dimethoxy-1,2,3,4-tetrahydroxy) -propyl) -pyrrolidyl 3) methyl-6,7-isoquinoline, mp 210 - 212 C., dimethoxy-17oxo-1,2,394 -tetrahydro Calculated (xH40),%: C 65.05, isoquinoline, mp 78 - 80 ° Cn 7.53, N 5.23.
Calculated (x H /),%: C 65.83; 30 Found,%: C 65.23; H 7.78; H 7.04; N 5.29; C1 6.70, N 5.030
Found,%: C 65.79; H 7.00; 2- (H- (3- (naphthyl-2N 5 03 C1 6.99.-oxy) propyl) -piperidyl-3) hydrochloride Hydrochloride 2- (No.- (3- (naphtsh1-2 ok 6,7-methylenedioxy-1-oxo-1,2,3,4si) -propyl) pyrrolides-3) methyl-6,7-35 tetrahydro-isoquinoline, m.p. 104 - methylenedioxy-1toxo-1,2,3,4-tetra- - 06 C. hydro-isoquinoline, m.p. 78 - 80 ° С “Calculated (х,%: С 66.09;
Calculated (xH40), Z: C 65.56; H 6.69; N 5.31; C1 6.72. H 6.48; N 5.46; C1 6.91. Found,%: C 66.19; H 6, J4;
Found X: C 65.44; H 6.32; 40 N, 5.24; C1 7.22. N 5.38; C1 7.13, Hydrochloride 2- | j (N- (J-naphthyl-hydroxychloride 2- (L- (2-iaftil-2-si) propyl) -piperidyl-3; -methyl-6,7-ethyl ) -pyrrolidyl-3) -methyl-6,7-dime-dimethoxy-1-oxo-1,2,3,4-tetrahydrotoxy-1,2,3,4-tetrahydro-isoquinoline, isoquinoline, m.p. 191 - 193 ° C.
m.p. 239 - 241 ° С.45 - Calculated (x Н20,%: С 66.34;
Calculated (xH40),%: C 64.48; H 7.23; N 5.15; C1 6.53. H 7.44; N 5.37; C1 13.91. Found,%: C 66S59; H 7.19;
Found,%: C 64.30; H 7.34; N 5.03; Cl 6.65. N 5.52; Cl 13,69. Hydrochloride 2- (L- (3- (naphthyl-2 Hydrochloride 2- (K-2-methyl-naph-5Q oxy) propyl) -hexahydroazepine-3) -tyl-1) -methyl) -hexahydroazepinil -3) - methyl-6,7-dimethyl-1-oxo-1,2,3,4-methyl-6,7-dimethoxy-1,2,3,4-tetra-tetrahydro-isoquinoline, m.p. 191 - hydro-isoquinoline, so pl. 182-184 ° -C. 193-C.
Calculated (x HgO),%: C 65.56; Calculated,%: C, 73.42; H 7.75; H 7.70; N 5.09; Cl 12.900N 5.52; Cl 6 „U9o
Found, JS: C 65.52; H, 7.57; Found,%: C, 73.37; H 7.67;
N 5 32 C1 12 72. 5.5.2; C1 7.120
Hydrochloride 2-CHN-i-Snaftip-2) - Dihydrochloride 2- (N- (2- (5-methi 1-6-propyl) -piperidyl-3) -methyl-6,7-dimethoxy-naphthyl-2 ) -ethyl) -hexahydroG
37156182338
azepinyl-3-methyl-6,7-dimethoxy Dihydrochloride 2- (Y- (2- (3,4-dimeg
1,2,3,4-tetrahydroisoquinoline, m.p.toxy-phenyl) -ethyl) -iperidl-3) me (170-172 ° C., 7-methylenedioxy-1,2,3,4-tet-
Rahydro-isoquinoline, so pl. 150 Calculated (x HjO),%: C, 64.96; 154 ° C. H 7.4U; N 4.73; C1 11, U8. Calculated,%: C 60.01; H 7.34;
Found C, 65.11; H 7.62; N 5.39; C1 13.64. N 4.95; C1 11.84. Found,% i C 59, Y6; H 7.41;
The dihydrochloride salt 2- (H- (3 (4-methoxy yN 5.25; C1 13.430
phenoxy) propyl) piperidyl-3) methyl 2-hydrochloride (No.- (3- (4-methoxy6, 7-dimethoxy-1,2,3,4-tetrahydro-isophenoxy) propyl) -piperidyl-3) - methyl | .quinoline, so pl. 189-191 ° C „6,7-dimethoxy ™ 1,2,3,4-tetrahydro-isoCalculated,%: C9.44; H 7.76; quinoline, m.p. ; 82 185 ° C. N 5.13j-C1 12, EI. 15 - Calculated, / „g C 61.05; H 7.09;
Found,%: C 59.55; H 7, V9; N 5.48; C1 13, Sb. N 5.12; C1 12.61. Found,%: C 6.10; H 6.95;
Dihydrochloride salt 2- (K-CH2- (3,4-dime-N 5,68; C1 13bE.
toxy-phenyl) -ethyl) -piperidyl - 3) me-Gitsrohlornd (3- (4-methoxy-
, 7-dimethoxy-1,2,3,4-tetrahydrin-20Phenoxy) propl) -pyrrolidyl-3) - ° mer-isoquinoline, so pl. 175-176 ° C., 7 dimetoksk 1 -oxo-1, 2,3,4- ™
Calculated,%: C 60.66; H 7.35; tetrahydro-isoquinolic, so pl. 142 N 5S3J; Cl 13.49.144 ° C.
Found,%: C 60,58; H 7.56; Calculated,%: C 6JS60; H 7.18;
N 5.32; Cl 13.22.25N 5.71; Cl 7522.
2-pN- (3- (3-MeTOKCH) dihydrochloride Found: C, 63.75; H, 7.12;
phenoxy) -propyl) -piperidyl-3) metshG | -N 5,64; Cl 7.32.
6,7-methylenedioxy-1,2,3,4 tetrahydro-2 pN- (3- (6-Metoxn- (naphthyl-2isoquinoline, 178-181 ° C. C.-oxy) propyl) -pyrrolidyl-3) -6 , 7 diRascited,%: C 59.08; H 7562; 30methoxy-1-goxo-1,2,3, -tetrahydroN 5.30; C1 14.31. Isoquinoline, i.e. 1 2-144 ° C. /
Found 7 ": C 58.90; H, 7.50; Calculated,%: C, 71.41; K 7.19;
N 5.40; C1 14.15. N 5S55.
The dihydrochloride salt is 2- (H (3- (3-methoxy- Found:%: C / 1.14; H 7.16;
phenoxy) -propyl) -piperidyl-3) -methylJ- 35 5.53.
6,7-methylenedioxy-1, 2,3,4-tetrahydro-Dhydrochloride 2 (N- (3- (4-methoxyisoquinoline, tLSh. 169-171 ° C. Phenoxy) -propyl) -pyrrolidyl 3 -methyl Calculated %; C 57aOZ; H 7.36; 6,7-dimethoxy-1,2,3,4-tetrahydro-isoN 5.11; C1 13.86.quinoline, mp 248 - 250 ° C.
Found,%: C 56.91; H 7.26; 40 Calculated,%: C 60.81; H 7.46;
N 5.15; C1 13.68.N 5.46; C1 13.81.
Dihydrochloride 2- (M- (2- (3,4-dime- Found:%: C 6i, 7U; H 7.61;
toxy-phenyl-ethyl-yperidyl-3 -N 5.48; C1 13,840
methyl 1-6,7-dimethyl-1,2,3,4-tetrahydride; hydrochloride 2- (M- (3- (4-methoxy-isoquinoline, mp 140-142 ° C. D5Phenrxy) propyl) - pyrrolidyl-3, calculated 7 ": C 62.00; H 8.34; tyl | -6., 7 dimethyl-1-oxo-1, 2,3,4-tetN 5.27; C1 13.44. Rahydro-isoquinoline, mp 118-121 s.
Found,%: C 61.85; H b, 27; Calculated,%: C 68.03; H 7.69;
N 5.31; C1 13, J3.N 6S10; Cl 7.72.
Dihydrochloride 2- (M- (3- (4-methoxy-JQ Found, / ": C 67, EO; H 7.71;
phenoxy; -propyl) -piperidyl-3; -methyl -N 6.04; C1 /, 90 „
6,7-dimethyl-1,2, J, 4-tetrahydro-iso-hydrochloride 2- (S - (/ .- (3,4-dimethocninoosy-phenyl) -ethyl) pnrrolidyl 3) methyl} Output 88.3 % of theoretical, 6,7-dime, toxi 1-oxo-1,2,3,4-tetrat. pl. 170-172 ° C. sehydro-isoquinoline, so pl. 116 - 118 ° C.
Calculated,%: C 63.14; H 8.24; Calculated,%: C 63.60; H 7.19;
N 5, b5; C1 14.31. N 5.71; C1 7.22a
Found,%: C 63.09; II 8.33; Found: C 63.82; H 7.32;
N 5.82; C1 14.02. N, 5.60; C1 7.66.
39 v 156182340
Dihydrochloride 2- | CHM- (3- (4-methoxy-methyl 5,6-dimethyl-1, J-dihydro-iso-
phenoxy) propyl) -pyrrolidyl-3) -me-indole, m.p. 118 - 127 C (amorphous).
, 7-dimethyl 1,2,3,4-tetrahydro-Calculated, 7 ,: С 59.03; H 7.54;
isoquinoline, m.p. 243 - 246 S.N. 8.98; C1 22.73
Calculated,%: C, 64.85; H 7.95; Found, X: C 58.93; H 7.48;
N 5.82; C1 14.73: N 8.84; C1 22.92.
Found,%: C 64.88; H 7.92; 2- 2- (M- (3- (Pyridyl-4.) - propyl) piN 5.63; C1 14.80. Peridyl-2-ethyl-5 6-dimetsh1-1,3-dihydrochloride 2- (H- (2- (3,4-dime-w hydro-isoindole, mp. 135-148 ° C
toxy-phenyl) -ethyl) -pyrrolidyl-3) - (amorph.).
methyl-6.7 dimethoxy-1,2,3,4-tetra-Calculated,%: C 54.59; H 8.24;
hydro-isoquinoline, so pl. 240 - 242 C, N 7.63; C1 19.33.
Calculated,%: C 60.81; H 7.46; Found,%: C 54.48; H 8.26;
N 5.46; C1 13.8} .15 N G1 19.60.
Found,%; C, 60.64; H 7.61; Trihydrochloride trihydrate 2- (NN 5.31; C1 13.50. (1 "(pyridyl-4) -methyl) -piperidyl-3) 2- (N-methyl -5.6 dimethoxy 1,3 dihydro-hydrochloride hemihydrate iso-Pyridil-4) -propyl) -pyrrolidyl-Zyndol, so pl. 176 - 189 C (amorphous).
methyl 1-5,6-dimethyl-1-oxo-1, -digchd-20 Calculated,%: C 4U, 7b; H 7.21;
po-Hsiimiona, 119 - 122 ° C. -N 7.91; C1 20.03.
Calculated,%: C 62.02; H 7.24;
N 9.43; C1 15.92. Found,%: C 49.93; H 7.12;
Found C, 62.25; H 7.47; N 8.00; C1 20.44.
N 9.39; C1 15,90.25 Dihydrochloride lolhydrate 2- (N-monohydrate dihydrochloride (2- (b, 7-dimethoxy-isoquinolyl-4) (N- (3- (pyridyl-3) propyl) piperidyl ™ ethyl) -piperidyl-3) methyl 5 , 6-dime3) -propyl-5,6-dimethoxy-1-oxo-1,3 tyl-153-dihydro-isoindole, so pl. 222 dihydro-isoindole, so pl. 118 - 121 С „236 С (amorphous).
Calculated,%: C 59.08; H 7.43; 30 Calculated,%: C 62.22; H 7.20;
N 7.95; C1 13.41. N 7.50; C1 15.83
Found,%: C 59.02; H 7.23; Found,%: C 62.01; H 7.64; N 7.12; C1 13.27. N 7.08; C1 15.79
2-N Dihydrochloride monohydrate Hemihydrate trihydrochloride 2 (N (3- (pyridyl-3) yropyl) ™ piperidyl-3) 35 O (pyrcdyl-4) methyl.) - piperidyl - 0-methyl-5, 6-dimethoxy-1 oxo- 1,3 di-methyl 5,6-methylenedioxy-1,3 dihydhydro-isoindole, m.p. .ro isoindole,. 215-225 ° C
Calculated,%: C 59.08; H 7.43; (amorphous).
N 7.95; C1 13.41. Calculated,%: C 53.68; H 6.22;
Found,%: C 5U, 02; H 7.23; 40 N 8.94; C1 22.63 „
N 7.12; C1 13.27. Found,%: C 5J, 60; H 6.45;
(6,7-Dimethoxy-isoquino-N 8.65; C1 22.28.
) -ethyl) -piperidyl 3) -measures 1-5.6 Monohydrate of 2-T trihydrochloride (Ndimethoxy 1-oxo-1, 3 dihydro isoin (3 (pyridyl-4) propyl) -pyrrolidil ™ 3; dol, t mp 85 - 88 ° C.45 Methyl2-6,7-dimethyl-1,2,4-tetrahydrin Calculated,%: C 65.39; H 7.19; po isoquinoline „
N 7.88; Yield 6J% of theoretical,
Found,%: C 65,16; H 7.27; mp. 254-256 ° C.
N, 7.53 Calculated,%: C 58.71; H 7.8U;
2- 2- (L- (3- (Niridyl 4) -propyl) -50 N 8.56; Cl 21.6b0
piperidyl-2) -ethyl-5,6-dimethyl-1-ok; Found: C 58.53; H 7.72;
co-1,3-dihydro-isoindole, so pl. 103 —N 8} 25; C1 21.53.
104 ° C. Trihydrochloride dihydrate 2- (N Calculated,%: C 76.68; H 8.49; (1 (pyridyl 4) -methyl) piperidyl-3; N 10,73.55 methyl-6,7-dimethoxy-1, 2,3,4 tetra: Found,%: C 76.57; H 8.54; hydro-isoquinoline, mp 158 - 1 ° C
N 10.60. (Amorphous).
Semi hydrate of trihydrochloride 2 (N-Calculated, 7,: C 52.42; .H 7.27;
(3- (pyridyl-4) -propshO-pyrrolidyl-3) N 7.97; C1 20.18 „
Found,%: C 52.55; H 7.49; N 7.57; C1 20.25
Trihydrochloride (N- (3- (pyridyl-4) propyl; -piperidyl-2) -, 7-methylenedioxy-1,2,3,4-tetrahydro-isoquinoline) trihydrate, mp 108 119 ° C ( amorphous.
Calculated,%: C 52.58; H 7.41; N 7.36; C1 18.62o
Found 7.1 C 52.56; H 7.25; N 7.38; C1 19.49.
Dihydrochloride monohydrate 2 (N- (3- (pyridyl 3) -propyl) piperidyl-3) - methyl-6,7-methylenedioxy 1,2,3,4-tetrahydro-isoquinoline, so pl. 126 - 138 ° С (amorphous „).
Calculated,%: C 59.50; H 7.28; N 8.67; C1 14.64.
Found,%: C 59.57; H 7.29; N 8.49; C1 14.51.
1-hydroxychloride 2- jj (N- (3- (pyridyl-3) propsh-piperidyl-3) methyl-6,7-dimeti.n-1,2,3,4-tetrahydro-isoquinoline, mp 138 - 154 ° C (amorphous).
Calculated,%: C, 61.66; H 7.86; N 8.62; C1 21.84.
Found,%: C S, 53; H 8.00; N 8.64; U1 21.35.
Dihydrochloride monohydrate of 2- (N- (3- (pyr i dyl-4) -propyl) -pyrrolidyl-3.) - methyl-6,7-dimethyl 1 oxo 1,2,3,4-tetrahydro-isoquinoline, t .pl. 74 - 86 ° C (amorphous),
Calculated,%: C, 61.53; H 7.5J; N 8.97; C1 15.13,
Found 7; C 61.42; H 7.62; N 8.83; C1 15.05,
tetrahydro-isoquinblin, t „pl. 142 158 ° C (amorphous).
Calculated,%: C 56.78; H 6.83; N 8.63; C1 14.58,
Found,%: With 56,4.3; H 6.59; N 8.66; C1 14.62o
Dihydrochloride 2 (N- (2- (6,7-dime toxi-isoquinol-4) -ethyl) -piperidyl JQ 3) methyl-6,7-dimethyl-1-oxo-1,2,3 tetrahydro-isoquinoline m.p. 148 162 ° C (amorphous).
Calculated,%: C 64.27; H 7.01; N 7.49; C1 12.65.
15 -, Found,%: C 64.11; H 7.20; N 7.59; C1 12.89 „
Dihydrochloride dihydrate (N- (3- (pyridyl-4-propyl) -piperidyl-2), 7-methylenedioxy-1-oxo-1,2, 2Q 4-tegrahydro isoquinoline, mp 115 128 ° C (amorph. ).
Calculated,%: C 56.59; H 7.03; N 7.92; C1 13.37.
Found,% i C 56.61; H 6.90; 25 N 7.84; C1 13.41.
Dihydrochloride 2 (N- (3 (pyridyl-3 -propyl) -piperidyl-3) -methyl-6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline dihydrate, tpl 118 - 3Q 127 ° C (amorphous).
Calculated, 7: С 60.00; H 7.85; N 8.39; Ci 14.16;
35
Found X: C 60.24; H 8.07; N 8.36; C1 14.6.
2- (K- (3- (pyridylpropyl) -pyrrolidyl-3; -metshG-6,7-me tylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline dihydrochloride, m.p. 102- 113 C
Dihydrochloride monohydrate 2- N- 40 amorFn) - (3- (pyridyl-3) -propyl) -pileridyl-3; - Calculated, 7, С С 59,22; H 6.27;
N 9.01; C1 15.20 „
Found,%: C 59.27; H b, 49;
methyl-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline, so pl. 140-148 ° C (amorphous);
Calculated (x 2HCl1xH20), X: C 58.36; H 7.25; N 8.16; C1 13.78
Found,%: C 58.35; H 7.32; N 8.04; C1 13.65.
2- (K (3- (pyridyl-3; - propyl) -piperidyl 3; methyl-6,7-methy-lendioxy-1-oxo-1,2,3,4-tetrahydroisoquinoline hydrochloride, t. pl 1 94-196 ° С (amorphous ...
Calculated 7.1 C 64.92; H 6.81; N 9.46; C1 7.98.
N 8.92; C1 14.48.
45 2- (No.-СЗ- (liridyl-propyl) -pyrrolidyl-3-methyl-7,8-methylenedioxy-2-oxo-1,3-dihydro-2H 3-benzazepine dihydrochloride, mp 132-141 C (. amorphous.)
Calculated,%: C 6U, 25; H 6.11; N 8.78; C1 14.82.
Found,%: C 60.00; H 6.40; N 8.52; C1 14,560
Dihydrochloride dihydrate 2- (N- (3 Found,%: C64,91; H6,, g--,., And.
N 9.67; C1 7.80. (Pyridyl-3) -propyl) -piperid 3-yl) 2- (N-methyl-7,8-dimethoxy-2-oxo-1,3-di- (1- (pyridyl 4) -methyl-piperidyl-3) methyl-6,7-dimethoxy-1-oxo 1,2,3,4-
hydro-2H-3-benzazepine, so pl. 128 - 134 ° С (amorphous) „
tetrahydro-isoquinblin, t „pl. 142 - 158 ° C (amorphous).
Calculated,%: C 56.78; H 6.83; N 8.63; C1 14.58,
Found,%: With 56,4.3; H 6.59; N 8.66; C1 14.62o
Dihydrochloride 2 (N- (2- (6,7-dimethoxy-isoquinolyl-4) -ethyl) -piperidyl- Q 3) -methyl-6,7-dimethyl-1-oxo-1,2,3,4 - tetrahydro-isoquinoline, so pl. 148 162 ° C (amorphous).
Calculated,%: C 64.27; H 7.01; N 7.49; C1 12.65.
5 -, Found,%: C 64.11; H 7.20; N 7.59; C1 12.89 „
Dihydrochloride (N- (3- (pyridyl-4-propyl) -piperidyl-2) -, 7-methylenedioxy-1-oxo-1,2,3, Q 4-terahydro isoquinoline dihydrate, mp 115-128 ° C (amorphous).
Calculated,%: C 56.59; H 7.03; N 7.92; C1 13.37.
Found,% i C 56.61; H 6.90; 5 N 7.84; C1 13.41.
2 (N- (3- (pyridyl-3 -propyl) -piperidyl-3) -methyl-6,7-dimethyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline dihydrochloride dihydrate, mp 118 - Q 127 ° C (amorphous).
Calculated, 7: С 60.00; H 7.85; N 8.39; Ci 14.16;
Found X: C 60.24; H 8.07; N 8.36; C1 14.6.
2- (K- (3- (pyridyl3) -propyl) -pyrrolidyl-3; -methyl-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline dihydrochloride, t mp 102-113 C
N 8.92; C1 14.48.
2- (No.-СЗ- (liridyl-4) propyl) -pyrrolidyl-3-methyl-7,8-methylenedioxy-2-oxo-1,3-dihydro-2H-3-benzazepine dihydrochloride, m.p. 132-141 C (. Amorphous.).
Calculated,%: C 6U, 25; H 6.11; N 8.78; C1 14.82.
Found,%: C 60.00; H 6.40; N 8.52; C1 14,560
Dihydrochloride 2- (N- (, g--,., And.
(pyridyl-3) -propyl) -piperid 3-yl) ethyl-7, 8-dimethoxy-2-oxo-1,3-di-
hydro-2H-3-benzazepine, so pl. 128 - 134 ° С (amorphous) „
43 156182344
Calculated,%: C L7.34; H 7.21; Dihydro chloride monohydrate a 3-Ј (NN 7.71; C1 13.02. (3- (pyridyl 4) -propyl) -pyrrg lidyl 3) Found: C 57.80; H 7.37; methyl-7,8-methylenedioxy-2-oxo - 1,3,
N 7.92; C1 13.06 .. 4,5-tetrahydro-2H-3-benzazepine,
 Dihydrochloride dihydrate 3 - (. M- (3-T. pl. 95 - 10 ° C (amorphous) „
(pyridyl-3) -propyl) -piperidyl 3) Calculated,%: C 57.8.3; H 6, L7;
methyl-7,8-dimethyl-2-oxo 1, .3-di-N 8.43; C1 14.22.
hydro-2H-3-benzazepine, so pl. 77 —Found, C 57.67; H 6.82;
86 ° C (amorphous). 10 N 8.27; C1 14.05.
Calculated,%: C 60.92; H 7.67} Semi Hydrochloride Hydrate (NN 8.19; Cl 13, (3- (pyridyl-4) propyl) -piperidyl-2) Found% 1 C 60.75; H 7.60} ethyl 7,8-dimethyl 2 oxo 1,3,4,5-het
N 8.37; C1 13,72. Hydrado-2H 3-benzazepine, m.p. 236 Dihydrochloride (No.- (3- (238 ° С „
Dil-4) -propyl) -gateridyl-2) EtuH {-Calculated,% g C 64.65; H 8.04;
7,8-dimethyl-2-oxy-1,3-dihydro 2H-3-N 8.37; C1 14.14.
Benzazepine, m.p. 118-130 ° C. Found, C 64.91; H 8.02;
(amorphous) N 8.25; CL 13.92
Calculated,%: C, 66.11; H 7.60; 20 3-Ј (№- (3- (pyridyl-3) N 8.56; C1 14.45; propyl) piperidyl-3) dihydrochloride chloride.
Found, Ј: C 65, U2; H 7.86; methoxy 2-oxo-1,3,4,5-tetrahydroN 8.33; C1 14.092H2-3-benzazepine, m.p. 11J - 122 С
Monohydrate 3-Ј (No.- (2- (b, 7-dimetok- (amorph.).
C-isoquinolyl-4; -ethyl) -piperidyl 3) 25 Calculated,%: C, 61.17; H 7.30;
methyl-7,8-dimethoxy-2-oXo-1, 8.23 g
hydro-2H-3-benzazepine, t, pl. 85-Found,% g C 61.31; H 7.50;
96 ° C (amorphous). N 8.28.
Calculated, 7.1 ° C, 67.7J; H 7.15; 3- (H- (2- (6,7-Dimethoxy-isoquinoN 7.64; 30 lil-4) ethyl) -piperidyl-3) methyl
Found,%: C 67.96; H 7.19; 7,8-dimethoxy-2-oxo-1,3,4,5-tetraN 7.75. Hydro-2H-3-benzazepine x 1/2 HgO,
Dihydrochloride monohydrate 3- 3- (Nt „Pl. 82 - 86 C (amorph.).
(3- (pyridyl-3) -propyl) -piperidyl-3) -Calculated,%: C, 66.40; H 7, b;
propyl-7,8-dimethoxy 2-oxo-1,3-di -, - N 7.48.
hydro-2H-3-benzazepine, so pl. 94 —Found,%: C, 66.26; H 7.50;
106 ° C (amorphous). N 7.59.
Calculated,%: C 60.64; H 7.45; 3 - (. 3- (NN 7.57; Cl 12.78. (Pyridyl-3) -propyl) -piperidyl-3) dihydrochloride dihydrate; Found: C 60.80; H 7.44; 40 propyl -, 8-dimethoxy-2-oxo-1,3,4, LN 7 46e C1 12 59. tetrahydro 2H-3-benzazepine m.p.
Dihydrochloride dihydrate (N-106 - 115 C (amorph.),
(3- (pyridyl-4) -propyl) -piperidic-2) Calculated,%: C 58, B3; H 7.89;
, 8-methylenedioxy 2 oxo-1,3-7,31; C1 12.34. dihydro-2H-3-benzazepine, so pl. 148-45 Found, X: C 58.46; H 7.61;
161 ° C (amorphous). N 7,14; C1 12,570
Calculated,%; C 57.56; H 6.87;
N 7.74; C1 13.07.Monhydrate of dihydrochloride 3- (H Found, / 5: C 57.72; H 7.03; (3-pyridyl-3) -propyl) -piperid% 3 N 7.61; C1 13, methylZ-7,8-methylenedioxy-2-oxoMonohydrate of 3- (M-1,3,4,5-tetrahydro-2H-3-benzazepine dihydrochloride,
(1- (pyridyl-4) -methyl) -piperidyl-3) -t.pl. 126-138 ° C (amorphous).
methyl-7,8-dimethyl 2-oxo-1,3-dihyd-Calculated. %: C 58.58; H 6.88;
ro-2H-3-benzazepine, so pl. 113 -N 8.19; C1 13.83.
127 ° C (amorphous). 55 Found,%: C 58.43; H 7, OU;
Calculated,%: C, 61.79; H 7.13; N 7.85; C1 13.71.
N 9.01; C1 15.20. Dihydrochloride monohydrate (N Found,%: C 61.55; H 7.32; (3- (pyridyl-4) -propyl) -piperidyl-2) N9, 04; C1 15.11 "ethyl-7,8-methylenedioxy-2-oxo-1,3,4-,
45 156182346
5 tetrahydro-2H-3-benzazepine, T. njr. 3-HN- (3- (pyridyl 132-146 C (amorph.) 3) propyl) -piperidyl-3) -methyl-3,8-hydroxychloride
Calculated,%: C 59.31; H 7.08; dimethyl-1,3,4,5-tetrahydro-2H-3-benzN 7.98; C1 13.46. Azepin, m.p. 184 - 196 ° С (amorphous).
Found,%: C 59.18; H 7.41; Calculated, X: C 60, H 8.16;
N 7.80; C1 13.25, N 8, Yu;, C1 20.49. ,
Dihydrochloride-3 (M-O- (pyridyl-3) -Found,%: C 60.28; H 8.25;
propyl) -piperidyl-3) methyl 7,8-di-N 8.00; C1 20.39.
methyl 2-oxo-1, 3,4,5 - tetrahydro-2H-3 2- (M- (3-. Naphthyl-2-hydroxy.) - propylJ
Benzazepine, m.p. 92 105 ° Сhexahydro-azepinyl 3) methyl | -6.7 (amorphous ,,,). Methylenedioxy-1-scso-1,2,3,4-tetrag
Calculated,%: C, 62.90; H 7.92; hydro-isoquinoline, t „pl. 74 - 76 ° C.
N 8.46; C1, 14.28; U 2 H40),%: C 64.45;
Found, C 63.19; H 7.90; 15 H 2 „02; N 5.01; Cl 6.34
N 8.45; Cl 14.30. Found, 7.1 C 64.32; H 7.20;
Trihydrochloride 3- monohydrate (N-N 5.28; Cl 6.44
(3- (pyridyl 4) -propal) -pyrrolidyl-3; 2- (m- (3- (Naphthyl 2) propyl) -pls methyl-7,8-methylenedioxy-1,3,4,5-tet rolidyl -3) -methyl -6,7-dnmethyl- 1 -ok-
Ragidro 2H-3-benzazepine, m.p. 96-20 cc-1,2,3,4-tetpagidro-isohiNoline,
103 ° C (amorphous.) T.pl. 72 - 76 ° C.
Calculated,%: C 55.33; H 6.97; Calculated, (x BUT),%: C 72.41;
N 8.06; C1 20.420H 7.75; N 5.82; Cl 7.36,
Found,%: C 55.06; H 7.28; Found: C, 72.27; H 7.85;
N 7.77; C1 20, N 5.70; C1 7.96.
Dihydrochloride 3- (K- (3- (pkri-Hydrochloride /). Ј№- (3- (5.6-dimethoxy-3) -propyl) -sheridyl-3) -methyl 1-naphthyl-2-oxy) -propyl ) -pyrrolidyl-3) 7, 8-dimethoxy-1, 4,5-tetrahydro-2H-methyl-6,7-dimethoxy-1-oxo-1,2,3,43-benzazepine, m.p. 208-210 ° C, tetrahydro-isoquinoline, so pl. 6U Calculated, and: p 62.89; H 7.91; 30 63 ° C.
N 8.46; C1 14.28. Calculated (x),%: C 63.20;
Found,%: C 62.70; H 7.53; N 7.01; N 4.75; C1 6.02 „
N 8.22; C1 14.50. Found,%: C 63.40; H 7.04;
Trihydrochloride. (, 49; C16s38o
Dil-4) -propyl; -piperidyl 2) -ethyl-35 Hydrochloride 2- (Y- (3 (5,6 dimethok 7, 8-methylenedioxy-1,3,4,5-tetrahydro "s-naphthyl-2-hydroxy ) -pt-opil) -hexagid ro2H-3-benzazepine, mp, 123-113 ° Cazepinyl-3} -meth., 7-dimethoxy-1 (amorph.) oxo-1,2,3,4- tetrahydro-isoquinoline,
Calculated: C 58.81; H 7.21; mp. 19U - 201 ° C.
N 7.91; C1 20, Calculated, C 66.15; H 7.23;
Found, C 58.51 .; H 7.41, N 4, b7; C1 5.92.
N 7.92; C1 19.86. Found; C 65.99; H 7.00;
Hemihydrate of trihydrochloride 3- Ј (N-N 4E44; C1 6,02 „
(3- (pyridyl- 3) - 1tropyl) - piperidyl- 3)
methyl -7.8 methylenedioxy-1,3,4,5-45 Dihydrochloride 2- (N- (3- (5,6-dimethra-tetrahydro-2H-3-benzazepine, m.p., tox-naphthyl-2-oxh; -propyl) -hex126 - 138 ° C (imorph.). hydro-azepinyl 3; -methyl-6,7-dime. Calculated,%: C 57.09; H 7.10; hydroxy 1,2,3,4-tetrahydro isoquinoline,
N 7.99; C1 20, .. pl. 114 - 116 ° L.
Found With 57.05; H 7.32; Calculated,%: C 61.97; H 7.56;
N 8.05; C1 20.37.N 4, C1 11.08;
Trihydrochloride 3- (2- (H- (3-pyri-Found,%: C 62.05; H /, 56;
Dil-4) -propyl) -piperidyl-2) -ethyl-N 4.06; C1 10.84s
7,8-dimethyl-1,3,4,5-tetrahydro-2H-3-Dihydrochloride-2-pN- (2- (4-methoxybenzazepine, mp. 180 - 182 ° C. 5g Phenyl-ethyl-pyrrolide .n-3) -methyl Calculated: C 62.96; H 8.22; 6,7-methylenedioxy 1,2,3, -tetrahydroN 8.16; C1 20.65. isoquinoline, mp 213 - 215 C.
Found,%: C 63.00; H 8.29;; Calculated,%: C 60.49; H 6.98;
N 8.16; C1 20, 5.87; C1 14.88.
47, 156182348
Found, from 60959 | H 6.96} Calculated,%: C 69.95; H 7.17;
N 5.845 C1 149U8.N 9E060
Hydrochloride 2 (M- (3- (3,4-dimetok- Found,% s U 70S00; H 7S03;
C-phenox-propyl) pyrrolidschm3). N 8,979
methyl} - 697 methylenedioxy- l-ojcco-hemihydrate of dihydrochloride 3- | 4N1, 2,3,4-tetrahydro-isoquinolinate t shi (2 (b methyl pyridine 2) eth1) pyrpro 108 - 110 ° C. lid-3 shea methyl} - 7,8-dimeschg-2 oxo calculated,% s C 5997b | H 6S74; 1, 3 dihydro-2H 3 benzazepine, so pl.
N 5.35; C1 7902 „h, 0 86 - 98 ° С (amorphous).
Found,%: C 60.07; H b, 87 s Calculated,%: C 63 S68; H 7.27;
N 5.23; C1 7.61.N 8.91 Ci 15.04.
Hydrochloride 2 (N- (2- (4-MeTOKCtr) Found,%: HSE39; H 7.43;
phenyl) -ethyl) -n rrolidyl-3) -methyl -N 8S87; Cl 14.93,
b-methylenedioxyN-oxo-H, 2S3S4 ° 15 Gitsrokhlorid-2- (KG- (3- (3-methyl-fettetrahydro-isoquinoline, t9pl0 105 -noxi.) - propyl) -piperidyl-3) -mett 108 ° C, 697-dimethoxy 1 oxo-1,2,3,4 tetra
. Calculated%: C 62.26; H 6.74; hydro-isoquinoline, m.p. 106 - 10U C
N 6.05; C1 7.97. (Amorphous,).
Found,%; C 62934 | H 6.74 | 20 Calculated ,,%: C 63595; H 7.75;
N 5988; C1 8, N 5E52; Cl 7S25,
(2- (6-methyl-pkridil-2) Found: C 64.66; H 7.91;
ethyl) pyrrolidyl-3) methyl - 7e8 di N 5S48; Cl 7.28,
methyl- ° 1 ,, 3; .4,5-tetrahydro-2H-3-benz hydrochloride 2- (No.- (2- (5 methyl-6
azepia x 2S5 HC1 x HЈUS t „pl" 80 -25 methoxy) naphth-2-yl) -pyrrolidyl 3) 91 ° C (. amorphous). methyl-6,7-methylenedioxy-1-oxo-1,2,
Calculated,%: C 61, 685 H 8s18j3,., 4-tetrahydrs-isoquinoling} m.p.
N 8.63; Cl 18S21,249 - 251 ° C0
Found,%: C 61.55; H 8S36; Calculated,%; C 68.43; H 6.53;
N 8.44; C1 18.10 -30 "B; C1 6.96.
Hemihydrate of dihydrochloride 3- (N-Found% s With 68.4 /; H 6.66;
(2- (6-methyl pyridyl- 2) otyl) pyrro N bs30; Cl 7s16c
lead-3) -methyl 7,8-dimethyl 2-oxo -Hydrochloride 2- (No. (3 (nastil-2) 1, 3,4,5-tetrahydro-2H J-benzazepine, propyl) -pyrrolidyl-3) - methyl -6. pl. 86 - 94 ° C (.amorph.) E methoxy 1 oxo-isoquinoline, t.cl. 84 Calculated, C 63.41; H 7, b6; 86 ° С
N 8.87; C1 14E97. - Calculated,%: C 67.88; H 7.26;
Found,%: C 63S52; H 7S14; N 5S46; Ci 6, V1.
N 8.81; Cl 14.94. Found,% g C 67.86; H 7.40;
2 (M-O- (6 methoxy naphthyl 2-hydroxy) 40 N 5.40; C1 7917.
propyl) -pyrrolidyl-3 mecsht -b, 7-dihydrochloride 2- (N- (3- (3,4-dimedimetip-1-oKCo-l, 2,3,4-tetrahydrotoxyphenoxy) propyl) -pyrrolidyl 3 ) isoquinoline, m.p. 102-104 eC0methyl 6.7 dimethoxy-1,2,3,4-tetraCalculated,%: (J 76E24; H 7968jhydro-isoquinoline, m.p. 220 - 221 C.
N 5, UZ.45 Calculated,%: C 5U, 20; H 6.88;
Found 7.1 C 75S90; H 7.62; N 5.31; Ci 13.44. N 5, U4 „
2- (M-3 (6-Methoxy-naphthyl-2-oxl)) - Found,%; C 59 S28; H 6997;
propyl) pyrrole, cyclic 3 methyl 6) 5.20j C1 13.44
dimethoxy-1,2,394-tetrahydro-isoqui etgd 2- Ј (no- (2- (3, 4-dimethoxyphenyl) noline, t.p., 106-108 „ethyl) -pyrrolidyl-3) -methyl -6, 7 di
Calculated,%; C, 73.44; H 7.82; methyl 1 oxo-1,2,3,4-tetrahydro-isoN 5.71 ocinoline, m.p. 168 - 17U S.
Found,%: C 73.26; H 7S72; Calculated,%: C 73.90; H 8.11;
N 5.81.55 N 6.63.
Monohydrate 3- (M- (3- (indolyl-3.) Found:%: C 73, Y6; H 8.11;
propyl) -pyrrolidyl 3U, | -methyl-7,8-me-N 6.55.
tylenedioxy-2-oxo-1,3,4,5-tetrahydride-hydrochloride 2-L (N-3- (4-methoxy-
ro-2H-3-benzazepine, m.p., 67 - 74 C. phenoxy) -propyl) -piperidyl-3) -methyl 49 156182350
6,7-dimethoxy 1-oxo-1,2,3,4-tetra-sword nrQ-1, J, 4, 5-tetrahydro-7,8-methy
hydro-isoquinoline, so pl. 98 - 102 ° C. Lenedioxy-2H-3-benzazepine, m.p. 10URas read,%: C 63.08; H 7.51; 111 ° C.
N 5.35; C1 7.02. Calculated%: C 74.39; H 7.80;
Found,%: C 62.87; H 7.69; N 5.42.
N 5.16; C1, 7.28; Found,%: C, 74.27; H 7.94;
Hydrochloride 2- (M- (3- (3-methoxy N 5.43 „
phenoxy) -propyl) -piperidyl-3) -methyl -2-XY- (3- (6-Methoxy-naphthyl-2-ok6, 7-dimethoxy-g-oxo-1,2,3,4-tetra-10 C) -propyl) -Piper Shil-3) -methyl -6,7
hydro-isoquinoline, so pl. 103- 105 ° C. Methylenedioxy-1-oxo-1,2,3,4-tetraCalculated,%: C 64.21; H 7.38; hydro-isoquinoline, m.p. 144 - 146SS.
N 5.55; Ci 7.02. Calculated,%: C 71.69; H b, 82;
Found,%: C 64.00; H 7.55; N
N 5.37; C1 7.12. 15% found: C 71.52; n 6.62;
The 2-G dihydrochloride (M- (3- (3-methoxy- 5.46.
phenoxy) -propyl) piperidyl-3) -methyl | 2-pY- (3- (b-methoxy-naphthyl-2-hydroxy 6, 7-dimethoxy-1,2,3,4-tetrahydro-iso-propyl; -hexahydro-azepinyl-3) quinoline, m.p. 170 - 173 ° C. methyl -5,6-dimethyl-1,3-dihydro-1 Calculated,%: C 60.43; H 7.70; 20 oxo-isoindole, mp 232 - 234 C.
N 5.22; C1 131.1. Calculated (x acetone),%: C 74.9 /;
Found,%: about 60.50; H 7.71; AND 8.14; N 5.14.
N 4.91; C1, 1.97; Found: C, 74.96; H 7.90;
Dihydrochloride salt 2- (K- (2- (3,4-dime-N 5.30.
 toxphenyl) -ethyl) -pyrrolidyl-3) -me-25 2- (H- (3- (l-Methoxy-caftyl-2-octyl} -6, 7-dimethyl-1,2,3,4-tetrahydro- C) -propyl) -piperidyl-3) -methyl-6,7 isoquinoline, so pl. 260 - 262 ° C. dimethoxy-1-oxo-1,2,3,4-tetrahydro Calcd.,%: C 64.85; H 7.96; isoquinoline, m.p. 124-126 ° C.
N 5.82; C1 14.73. Calculated,%: C 71.79; H 7.38;
Found,%: C 64.60; H “, 11; 30 N 5.40.
N 5.91; Cl 1 -t, 67. Found,%: C 71.83; H 7.33;
3- G ((3- (6-Methoxy-naphtshg-2-ok 5.21.
C) -propyl) -hexahydro-azepinyl-3) -3 (- (3- (5t6-Dimethoxy-naphthyl-2methyl-7, 8-dimethoxy-1,2,3,4-tetra-oxy) -propyl) - hexahydro-azepinyl-3) hydro-2H-3-benzazepine, m.p. 98-35 MeTpmJ 1,3,4,5-tetrahydro-7,8-dime100 ° C. Toxy-2H-3-benzazepine, m.p. 94 Calculated (x H20),%: C 71.97; 9b ° C.
H 8.42; N 5,09. Calculated,%: C 72.57; H 8.24;
Found,%: C 72.07; H 8.23; N 5.98,
. N 5,10.40 Found%: C 72.56; H 8.35;
2- (H- (3- (6-Methoxy-naphthyl-2-ok-N
si) propyl-hexahydro-azepinyl-3) -2 (H- (3- (b Methoxy-naphthyl-2-oxmetch -1, 3, -dihydro-5,6-dimethoxy-si) -. 1propyl) -hexahydro - azepinyl-3) isoindole, so pl. 104 - 146 ° C.methyl -1,3-dihydro-5,6-dimethoxy-1 Calculated,%: C 73.7 "; H 7.99; 45 oxo-isoindole, m.p. 265 - 267 ° C.
N 5.55. Calculated (x 2HЈ0),%: C 67.13;
Found,%: C 73.63; H 7.99; n /, 63; S 5.05.
N 5.39. Found,%: C 67.11; H 7.64;
3-L dihydrochloride monohydrate (N - 5.07.
(3- (indolyl-3) -propyl) -pyrrolidyl-3) -JQ
methyl 3-7,8-dimethyl-1,3,4,5-tetrahydrihydrochloride 2- (K7- (3- (5,6-dimero-2H-3-benzazepine, so pl. 168-toxy-naphthyl - -oxy) -propyl) -hexa17U ° C. Hydro-azelnyl-3) -methyl -5,6-dimetok
Calculated,%: C, 66.39; H 8.16; Ci-1,3-dihydroisoindole, m.p. 172 N 8.29; C1 13.EU.55 177 ° C.
Found,%: C, 66.29; H 8.44; Calculated (x),%: C 61.43;
N 8.08; C1 14.08. H 7.41; K 4.7; C1 11.33.
3- (L- (3- (6-Methoxy-naphthyl-2-ca-Found, /,: C 1, 0; H 7.71;
si) propyl) hexahydro-azepinyl-3) -N 4.59; C1 11, b.
51 156182352
Hydrochloride 2 (H- (3- (5,6-dimetok) Calculated,%: C 62.58; H 7.67;
C naphthyl-2 hydroxy) propyl) hexahydro-N 5S21; C1 6.83.
aepecin-3) -methyl 5,6-dimethox1G 1,3-Found,% i C 62.44; H 7.68;
dihydro-1-chjsoisoindole, mp 215 -N 4.91; Cl 6.81.
223 ° С “Hydrochloride 2- (M- (2- (4-methox | g °
Calculated (x H20),%: C 61587 | phenyl) ethyl) hexahydro-azepinyl-3) H 7.30; N 4.50; C1 5.70. Methyl 6,7-dimethoxy-1-to-co-1, 2, 3, 4 Found,% C 62 „08; H 7915 tetrahydro-isoquinoline, t.cl „110N 4,55; C1 5.80. W 113 ° C.
Dihydrochloride 2 monohydrate (N-Calculated,%; C 61.75; H 7.87;
(3- (indolyl-3) -propyl) pyrrolidyl 3) N 5.28; C1 7E25.
methyl-5,6-dimethoxy-1,3-dihydro-iso-Found%: C 61.84; H 8.02;
indole, m.p. 262 - 264 ° C. .N 5S16; CL 7.22,
Calculated,%: C 61E17 | H 7.30 j15 Hydrochloride 2- (H- (2- (3,4 dimetokN 8.23; C1 13.89.si-phenyl) ethyl) hexahydro-azepinyl Found,%; U 61.34; H 7.36; 3) -methyl-6,7-dimethoxy-1 oxo-1,2,3,
No. 7 S92; Cl 13.90.4 tetrahydro-isoquinoline,. 107 3-PY- (3- (5,6-dime-1110 dihydrochloride).
tox-naphthyl-2-ox) -propyl) hexa-2Q Calculated,%: C b2, b1; H 7.69;
hydro-azepinyl-3) -methyl 1,3,4E5-N 5.215 Cl 6.60.
tetrahydro 798-dimethyl 2H-3 Bonsaze-Found,%: C 62.78; H 8.00;
Pinae m.p. 138-144 ° C „N 5.00; Cl 6.43l
Calculated,%: C 67S64 H 8.01 V | Hydrochloride 2- (L- (2- (3,4-dimetok
N 4S6 Cl 11E74.25 syphenyl) -ethyl) -hexahydro-azepinylKadeno,% C 67.73 | H 8.26; 3) -metip} -6,7-dimethyl 1- oxo-1,2,3,4N 4,47; C1 11.50 "tetrahydro-isoquinoline, so pl. 162 Hydrochloride 2-Ј (H - ((4-methoxy 163 ° C.
phenyl) eth1) texahydro-azelinyl-3) -Calculated,%: C 66.57; H 8.18;
methyl -b57 ™ methylenedioxy-1-oxo-30 N 5.54; C1 7.02.
1,2,354 tetrahydro-isoquinoline, m.p. Found,% s C 66.67; H 8.47;
101 - 105 ° C. N 5.35; C1 7.11.
Calculated,%; C 62.44; H 7.26; 2- (N- (3- (3-methyl-FeN 5.60; Cl 7S50 "noxy) -propyl) -hexahydro-azelinyl-3) hydrochloride -
Found% S С 62,62; H 7.27; 35 type 697 methylenedioxy-1-oxoN 5.48; C1 7,66.1,2,3,4-tetrahydro-isoquinoline, so pl.
Hydrochloride 2- | (N- (3- (4-MeTOKCH 159 - 161 C.
phenoxy) -propyl) -hexahydro-azepi-Calculated,%: C L5.37; H 7.31;
nyl-3) methyl ™ b, 7-methylevdioxy 1 N 5.64; C1 7.28.
oxo-1,2,3,4 tetrahydro isoh.inoline, 40 Found: C, 65.44; II 7.40;
m.p. 123: 126 ° C.N 5.39; C1 7.23.
Calculated,%: C, 62.23; H 7.1 O; 2- (H- (3- (3-methyl-FeN 5.37; Cl 7, U5 noxy) -propyl) -hexahydro-azepine-3 hydrochloride) Found: C, 62.42; H 7.34; chetyl-6,7-dimethoxy and 1-oxo-1,2,3,4N 5.30; Cl 6.94.45 tetrahydro-isoquinoline, so pl. 107 Hydrochloride 2-Ј (and- (3- (4-methoxy-111 ° C.
phenoxy) propyl) -hexahydro azepi Calculated,%: C 65.67; H 7.87;
nyl-3) -methyl b57-dimethyl-1 oxo-N 5.47; C1 7.05. Have
1,2,3,4-tetrahydro-isoquinoline, mp. Found,%: C 65.47; H 8.00;
172 - 173 ° C. -50 N 5.50; C1 6.97.
Calculated,%: C 69.04;% H 8.07; - Hydrochloride-2 (N- (J- (3.4 9 46tilenN 5.75; Cl 7.28o dioxyphenoxy-nropida-hexahydroxy)
Found%: C 69.06; H 8.25; azepinyl-3) -methyl-6,7-dimethyl-1-okN 5.57; (J1 7.39., 2,354-isoquinoline tetrahydr,
Hydrochloride 2-t (N- (3- (4-MeTOKCH 55 23 - 12 ° C.
phenoxy) -propyl) -hexahydroazepi, Calculated,%: C H 7S57;
nyl-3) -methyl) -6,7-dimethoxy 1-oxo-N 5.39; C1 6.83.
1,2,3,4-tetrahydro-isoquinoline, mp. Found,%: C, 64.88; H 7.59;
Ts5 - 120 ° C.N 5.29; Ci 7.18.
53 156182354
Hydrochloride 2- (M- (3- (3,4-dimetho- Calculated,%: C 58.05; H 7.40;
C-phenoxy) -propyl,) - hexahydro-azepi-N 7.52; C1 12.69
nyl-3 methyl-6.7 dimethoxy-1-oxo-found;% C 57.94; H 7.55;
1,2,3,4-tetrahydro-isoquinoline, .N 7.75; 01 12.42.
m.p. 101 - 105 ° C. Dihydrochloride 3-((N- (3 Calculated,%: C 62.61; H 7.59; (pyridyl 3) -propyl) -hexahydro-aseN N 5.01; C1 6,46 „pinyl -3) -methyl-7,8-dimethoxy-2-oxo Found,%: C 6 / ;, 56; H 7.76; 1,3,4,5-tetrahydro-2H-3-benzazepine,
N 4.94; Ci 6.39, 10 m.p. 119 - 121 ° C.
Hydrochloride 2- (H- (2- (3,4-dimetok-Calculated,%: C 57.85; H 7.73;
Cp-phenyl) -ethyl) -hexahydro-azepi. N 7.49; C1 12.65.
nyl-3-methyl-5,6-dimethoxy-1-oxo-found;% J C 57.74; H 7.79;
1,3-dihydro-isoindole, so pl. 150 -N 7.23; C1 12.50.
151 ° С.15 "Nonhydrate of trihydrochloride 3- (N Calculated,%: C 61.99; H 7.57; (3- (pyridyl-3) -propyl) teksahydroN 5.35; Ci 6,77. Azepinyl-3) -methyl 7.8 dimethoxy Found,%: C 61,89; H 7,48 J1,3,4,5-tetrahydro-2H-3-benzazepine,
N 5.17: C1 6.52 „/ t.pl. 139 - 141 ° C.
Hydrochloride (C– (3- (3-methyl-phe-20) Calculated, X: C, 57.39; H, 7.85;
noxy) propyl) hexahydro-azepinyl-3) - N 7.43; C1 18982 ..
Methl 5,6-dimethoxy-17o with a co 1,3.-di-Found%: C 57.42; H 8.15;
hydro-isoindole, so pl. 95 - 100 ° C. N 7.56; C1 19.04
Calculated,%: C, 63.95; H 7.75; 2-Ј (N- (1N 5.52; C1 7.25.25 (pnridyl-3) -methyl) -pyrrolidyl-3) dihydrochloride dihydrate; Found: C 64.09; H 7.64; methyl 6,7-methylenedioxy-17 ° KcoN 5.35; C1,3701,2,3,4-tetrahydro-isoquinoline,
Hydrochloride 2 (M- (3- (4-methokei T. pl. 91 - 93 C.
phenoxy) -propyl) -hexahydro-azepi-Calculated,%: C 53.17; H 6.16;
Nyl-3) Me1SH1 - 5,6-dimethoxy 1-o1sso-30. d
1,3-dihydro-isoindole, so pl. 107 -Found,%: C 53.31; H 5.93;
 t ° C.N 8.71; C1 15.01.
Calculated,%: C, 61.99; H 7.51; Trihydrochloride 2- (1h- (1- (pyridylN 5.35; C1 7.02 „3) -methyl) -pyrrolidyl 3) -methyl1-6.7 Found,%: C 62.07; H 7.37; 35 methylene-Dioxy 1,2,3,4-tetrahydro-isoN 5 28 C1 7 31.quinoline x 1.3 hydrate, mp. 178 g- (3- (3,4-methi-1a1 hydrochloride slendioxy-phenoxy-propyl) -hexagide) Calculated, l: C 51.70; H 6.41;
ro-azepinyl-3) -methyl-5,6-dimethoxy- 8.61; C1 21.80.
1-OXO-1,3-dihydro isoindole, t..40 Found,%: C 51.63; H 6.62;
104 - 107 ° C.N. 8.45; C1 21.07
Calculated,%: C 60.38; H 6.94; 3- (N- (2N 5.20) dihydrochloride dihydrate; C1 7.31. (6-methyl-pyridyl-2) -ethyl) -hexahydro
Found,%: C 60.40; H 7,15 jazepinyl-3) -methyl-7,8-dimethoxy-2N 4,95; C1 .45 oxo-1,3-dihydro-2H-3-benzazepine,
Hydrochloride 2- H - (. 3- (3,4-methi-t Pl. 134 - 136 ° С.
lendioxy phenoxy; propyl) -hexagide-Calculated,%: C 58.05; H 7.40;
ro-azelinyl-3) -methyl-5,6-dimethoxy-N 7.52; C1 12.69
1-oxo 1,3-dihydro-isoindole, mp. Found,%: C 58.15; H 7.60;
112 - 116 ° C.50 N 7.45; C1 12.4b.
Calculated,%: C, 62.23; H 7.15; 3- (Di- (2- (6-methyl
N 5.37; C1 7,050 pyridyl-2) -ethyl) -pyrrolidyl-3) -me-
Found,%: C 62,16; H 7.25; thyl-7,8-dimethoxy-2 oxo 1,3-dIgidN 4.96; C1 7.03. , po 2H-3-benzazepine x 1.5 hydrate,
Dihydrochloride dihydrate 3- (N- (3-55 t "Sq. 78 - 80 ° С.
(Pyridyl-3) -propyl) -hexahydroaze-Calculated,%: C 57.58; H 6.96;
pinyl-3) -methylZ 7,8-dimethoxy-2-ok-N 8.06; (L 13.6U.
co-1,3-dihydro-2H-3-benzazepine; Found,%: C 57.40; H 7.18;
m.p. 106 - 108 ° C.N. 8.24; C1 13.39.
55156182356
Dihydrochloride-3- {XY- (2- (6-methyl hydro-2H-3-benzazepine, mp 125 pyridyl-2) ethyl) -hexahydro-azepi-. ) methyl-7,8-dimethoxy-2-oxo-1, -3,4,5-tetrahydro 2H-3-benzazepine x x 2.5 hydrate, so pl. 112 - 114 s.
Calculated,%: C, 56.93; H 7.78; N 7.38; C1 12.45
Found,%: C 56.83; H 8.04; N 7.43; C1 12.26.
3-Ј (N- (2- (6-methyl-pyridyl-2) -ethyl) -hexahydro-azepinyl-3) -methishG-7,8-dimethoxn 1,3,4,5-tetrahydro-dihydrate trihydrochloride dihydrate 2H-3-benz azepine, m.p. 148 - 150 ° C.
Calculated,%: C 55.61; H 7.95; N 7.20; C1 18.2%; Found,%: C 55.72; H 8.10; N 7.03; C1 18.00,
Dihydrochloride dihydrate (N- (2 (6-methyl-pyridyl-2) -ethyl) -lirrolyl-3) -methyl-7,8-dimethoxy-2 oxo-1,3,4,5-tetrahydro-2H- 3-benzazepine, so pl. 87 - 90 ° C.
Calculated,%: C 56.38; H 7.38; N 7.89; C1 13.31.
Found,%: C 56.33; H 7.53; , N 8.09; C1 13.43.
3-Ј (N- (2- (6-methyl-pyridyl-2) -ethyl) -pyrrolidyl-3) -methyl-, -8-dimethoxy-1,3,4,5-tetrahydro-2H trihydrochloride dihydrate -3-benzazepine, mp: 225 - 227 ° C.
Calculated,%: C 54.10; H 7.62; N 7.57; C1 19.16.
Found,%: C 54.18; H 7.55; N 7.51; C1 1U, 30.
Monohydrate of hydrochloride (N- (3- (indolyl-3) -propyl) -pyrrolidyl-3) - methyl-7,8-dimethyl si-2-oxo-1,3,4,5-tetrahydro-2H-3-oenzazepine m.p. 128-130 ° C.
Calculated,%: C 65.16; H 7.42; N 8, U; Cl 6,870
Found%; C 65.12; H 7.55; N 8.11; C1 7.06 „
3-Ј (H- (3- (indolyl-3) -propyl) -hexahydro-1288 ° C dihydrochloride monohydrate)
Calculated,%: C, 62.44; H 7.6 /; N 7.80; C1 139160
Found,%: C 62.35; H 7.87; N 7.59; C1 13.67 „
Dihydrochloride monohydrate 2-Ј (N- (3- (indolyl-3) -propyl) -pyleridyl-3) - 10 methyl-6,7-dimethyl-1,2,3,4-tetrahydro-isoquinoline, t „ square 198 - 201 ° C.
Calculated,%: C, 66.38; H 8.16; N 8.29; C1 14.00.
Found,%: C, 66.29; H 8.21; 15 N 8.46; C1 13.82s
Dihydrochloride 11 hemihydrate, ca (N- (3- (indolyl-3) -propyl) -pyrrolidyl-3) - methyl-6,7-dimethyl-1, 2,3,4-tetrahydro-ro-isoquinoline, m.p. 143-145 ° C. 2o Calculated,%: C 67.06; H 7.92; N 8.69; C1 14.66.
Found,%: C, 66.92; H 8.07; N 8.48; C1 14.87.
Z-SM-SZ-Sindolyl-3) dihydrochloride-25 propyl) -pyrrolidyl-3) -methyl-7,8-methylenedioxy-1,3,4,5-tetrahydro-2H-3-benzazepine x 1.5 hydrate, m.p. 191 - 193 ° C.
Calculated,%: C 61.01; H 7.21; 30 N 7.90; 01 13 „34.
Found,% C 60.90; H 7.27; N 7.85; C1 13.70;
Dihydrochloride (N- (3- (indolyl-UZ) -propyl) -hexahydroazepine-3) -methyl-7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepine monohydrate, t., Pl . 158 - 160 ° С.
Calculated,%: C, 63.58; H 8.00; N 7.41; C1 12.51
Found,%: C 63.41; H 8.18; N 7.36; C1 12.23.
The proposed compounds have valuable pharmacological properties, in particular, with minor central side effects, they reduce blood pressure and, particularly, prolong the frequency of heart contractions, as well as reduce symptoms.
40
45
azepinyl-3) -methyl-7,8-methylenedioxy-50 V acid ° P ° «e heart. On their Oiologichesk1, 3,4,5-tetrahydro-2H-3-benzazepina, so pl. 155 - 158 ° С „
Calculated,%: C, 62.26; H 7.50; N 7.63; C1 12.88.
Found,%: C 62.31; H 7.82; N 7.40; C1 12.89.
3- (N- (3- (Indolyl-3) -propyl) -pyrrolidyl-3) dihydrochloride monohydrate - methyl | -7,8-dimethoxy-1, 3,4,5-tetra55
The following properties were investigated, for example:
A - Hydrochloride 3- (H- (2- (naphthyl--2) -ethyl) -pipedshg-β-methyl 7,8-dimethoxy-2-oxo-1,3,4,5-
tetrahydro-2H-3-benzazepine,
B - Hydrochloride-3 (H- (2- (5-methyl-6-methoxy-naphthyl-2) ethyl) -liperidyl-3) methyl 3 7.8-dimethohydro-2H-3-benzazepine, t. square 125128 ° C.
Calculated,%: C, 62.44; H 7.6 /; N 7.80; C1 139160
Found,%: C 62.35; H 7.87; N 7.59; C1 13.67 „
Dihydrochloride monohydrate of 2-Ј (N- (3- (indolyl-3) -propyl) -pyleridyl-3) - methyl-6,7-dimethyl-1,2,3,4-tetrahydro-isoquinoline, t „pl . 198 - 201 ° C.
Calculated,%: C, 66.38; H 8.16; N 8.29; C1 14.00.
Found,%: C, 66.29; H 8.21; 5 N 8.46; C1 13.82s
Dihydrochloride 11 hemihydrate, ca (N- (3- (indolyl-3) -propyl) -pyrrolidyl-3) - methyl-6,7-dimethyl-1, 2,3,4-tetrahydro-ro-isoquinoline, m.p. 143-145 ° C. o Calculated,%: C 67.06; H 7.92; N 8.69; C1 14.66.
Found,%: C, 66.92; H 8.07; N 8.48; C1 14.87.
Z-SM-SZ-Sindolyl-3) dihydrochloride-5) propyl) -pyrrolidyl-3) methyl-7,8-methylenedioxy-1,3,4,5-tetrahydro-2H-3-benzazepine x 1.5 hydrate, m.p. 191 - 193 ° C.
Calculated,%: C 61.01; H 7.21; 0 N 7.90; 01 13 „34.
Found,% C 60.90; H 7.27; N 7.85; C1 13.70;
Dihydrochloride (N- (3- (indolyl-UZ) -propyl) -hexahydroazepine-3) -methyl-7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepine monohydrate, t., Pl . 158 - 160 ° С.
Calculated,%: C, 63.58; H 8.00; N 7.41; C1 12.51
Found,%: C 63.41; H 8.18; N 7.36; C1 12.23.
0
The proposed compounds have valuable pharmacological properties, in particular, with minor central side effects, they reduce blood pressure and, particularly, prolong the frequency of heart contractions, as well as reduce symptoms.
In acid ° P ° "e heart. On their iolog
The following properties were investigated, for example:
A - Hydrochloride 3- (H- (2- (naphthyl--2) -ethyl) -pipedshg-β-methyl 7,8-dimethoxy-2-oxo-1,3,4,5-
tetrahydro-2H-3-benzazepine,
B - Hydrochloride-3 (H- (2- (5-methyl-6-methoxy-naphthyl-2) ethyl) -liperidyl-3) methyl 3 7.8-dimethok10
20
25
si-2 oxo-1,3,4b-tetrahydro-2H 3- «with enzazepine.
B - 3-CHI- (2- (6-methoxy-naphthyl-2) -ethyl) -liperidyl-2) -ethyl-7,8-dimethoxy-2-oxy-1, 3,4,5 tetrahydro hydrochloride -2H 3-benzazepine,
G - Hydrochloride 2- (L (2- (6-labels of s-naphthyl 2) - ethyl teksahydroazepinil-3-metshl-b, 7-methylenedioxyg-1-oxo-1s2,3,4 TeTpa hydro-isoquinolic,
C - Hydrobromide (2- (naphthyl -2) ztil) - hexahydra-a:; decinyl- -3) -methyl), 7 methylentiox, 2,3, a-techravdro-n-hinolchna.
E - 2-f (N- (2 - (3,4-dimethoxy-phenyl) ethyl) -pkpridid-3) dihydrochloride-methyl 1-6,7-dimethyl-1,2,3,4-tetrahydrochloride isoquinoline a.
G - 2-Ј (- (2 (3,4-di methoxy-phenyl) ethyl) hydrochloride; -liperidyl-3) methyl 1-6,7-dimethyl-1-oxo-1,2 j3, (-tetrahydro-nzohinolinao
3 - Hydrochloride-ad 2 (N - ((4 MeTOiC-si-phenocol) -propyl) -piperidine- - $ Q -3) methyl-6.7 Dimet. P -1-oxo- 1,2,3,4 -tetrahydro-kzokhinolika.
And ha Hydrochloride 3- (L- (4- (thienk--2) butyl) -piperidyl-3) -methyl-7} 8-dimethoxy - 2 "oxo-1, 3, c, 5 tetrahydro-2H 3 -benzazelina.
K - Hydrochloride 3- (No.- (2 (benzo-7, furyl-2) ethyl) -pyleridyl-3) - methyl-7,8-dimethoxy-2-oxo-1,3,4,5-tetrahydro-2H-3 benzazepine
L - Hydrochloride 3 pm- (2- (belzo thienyl-3) -ethyl) -piperidyl 3) - methyl-7,8-dimet 1 hydroxy-2-oxo 1, 394,5-tetoagidro ™ 2H 3 benzazepine.
M - Hydrochloride 1 C (hg7-di-methoxy) 3,4-dihydro "2H-isoquinolin-1 - it-2-yl1-3 Gy-methyl H- 2- (3,4-dimrthoxyphenyl) -eth-D-amino propane ( known),
Effect on heart rate in rats.
35
, 0
45
50
In two rats with an average weight of 250–300 g, the effect of VBR ™ of the above-mentioned substances on the heart rate was investigated. For this htys
anesthetized with pentobarbital (50 mg / kg of intraperitoneal intraperitoneal and 20 mg / kg subcutaneously). The test substances in the form of an aqueous solution were injected into the celiac vein (0.1 ml / 100 g).
Blood pressure was measured using a cannula inserted into the carotid artery, and the heart rate was recorded using electrocardiogram abducted by needle-like electrodes. The heart rate of animals during the control period was between 350 and 400 beats / minute (o0 / min) L
The table shows the results.
substance
Dose, mg / kg
Decrease in heart rate, b; / min, after 20 min
five
Q
five
A B C G1
D
YO F 3
II to l
M
5.0 L, C 5 9 C 5.0 5.0 5.0 5.0 5.0 5.0 2.5 2.5 5.0
-259 -218 -194 -123 -150 -120 -101 -180 -253 -156 -163 - 73
0
five
The proposed compounds are: a group of low toxic substances.

权利要求:
Claims (1)
[1]
Invention Formula
Method for preparing cyclic amine derivatives of formula I
. (CH2) m
vi
R,
BUT /
G N-E-CiF li-U - - /
(Hr) n
R,
at
where A is the group —H2-,
tsl-CH-CP, B - group-CH4-,
-s-scg
sn, -, - with
or NgCO-, and the carbon atom denoted by Oukza x is associated with a secondary core; E - unbranched alkyls with 1-J carbon atoms, unsubstituted or for: else al-Kiirioiv with 1-3 carbon atoms;
, t - alkylene with 1-6 carbon atoms; lower alkyl or lower alkoxy group, or together form methylenedioxygroup; R - naphthyl or naphthyloxy group, unsubstituted or mono- or disubstituted by lower alkyl or alkoxy, benzyloxy group, furyl, thienyl, indolyl, pyridyl, unsubstituted or substituted by lower alkyl-, scrap, isoquinolyl5 substituted by two lower alkoxy groups, benzo) e furyl or benzo V thienyl, unsubstituted or substituted by lower alkoxyl or methylsulphonyloxy group, or phenyl substituted by nitro, amino, acetylamino, lower alkyl or lower alkoxy, phenyl substituted by two lower alkoxyl groups pamy or one methylenedioxy group, phenoet xygroup, substituted by lower alkyl or lower alkoxy group, phenoxy group, substituted by one methylenedioxy group or two lower alkyl or alkoxy groups or two halogen atoms, an aniline group substituted by two lower alkyl or alkoxy groups, substituted by an atom nitrogen by lower alkyl when B is a group —CH — and —CO —;
t is 1,2,3,4,5 or b;
n is 0, 1, 2 or 3, and the sum m + n should be 3,4,5 or 6,
or their acid-additive salts, characterized in that the compound of the general formula II
nh-a /
but.
/ №g} tp X (CH,) HRP
NH,
0
five
0
0
where Ri, R-, A, B, Es
, the type has the indicated values
possibly containing a protective group, is reacted with a compound of general formula III
ZrG-R,
Where R and G have the indicated meanings; a nucleophilic leaving group, such as a halogen or sulfonyloxy group, possibly containing a binding group, followed, if necessary, by cleaving the protective groups and isolating the desired product in free form or as a salt, or by reducing the resulting compound of formula I, where R is substituted 5 a phenyl nitro group, to a compound forms a mule in which R is an amino-substituted phenyl group, or by acylation of a compound of formula I, where R is an amino-substituted phenyl group, to a compound of formula I in which R is an acetylamino substituted a phenyl group.

类似技术:

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公开号 | 公开日 | 专利标题

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SU1561823A3|1990-04-30|Method of producing derivatives of cyclic amine or their acid-additive salts

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IE63766B1|1995-06-14|Benzoxazine derivatives

同族专利:

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公开号 | 公开日

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CA1330993C|1994-07-26|

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DK282188D0|1988-05-24|

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DE3717561A1|1988-12-08|

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NZ224756A|1991-02-26|

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IE881559L|1988-11-25|

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KR960009432B1|1996-07-19|

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FI882418A|1988-11-26|

---

EP0292840A2|1988-11-30|

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AU607765B2|1991-03-14|

---

AT126225T|1995-08-15|

---

IN169514B|1991-11-02|

---

FI94343B|1995-05-15|

---

DD284678A5|1990-11-21|

---

HUT46906A|1988-12-28|

---

NO171017B|1992-10-05|

---

EP0292840B1|1995-08-09|

---

PT87567A|1989-05-31|

---

CA1287226C|1991-08-06|

---

IL86477D0|1988-11-15|

---

IE68842B1|1996-07-10|

---

JPS6445381A|1989-02-17|

---

NO171017C|1993-01-13|

---

FI94343C|1995-08-25|

---

DE3854280D1|1995-09-14|

---

AU1656288A|1988-12-01|

---

IL86477A|1992-07-15|

---

FI882418A0|1988-05-23|

---

EP0292840A3|1990-04-11|

---

NO882258L|1988-11-28|

---

DK282188A|1988-11-26|

---

PT87567B|1992-09-30|

---

ZA883680B|1990-01-31|

---

NO882258D0|1988-05-24|

---

ES2076147T3|1995-11-01|

---

GR3017550T3|1995-12-31|

---

JP2634190B2|1997-07-23|

---

HU198201B|1989-08-28|

---

KR880013924A|1988-12-22|

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法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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DE19873717561|DE3717561A1|1987-05-25|1987-05-25|INDOL, ISOCHINOLINE AND BENZAZEPINE DERIVATIVES, MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF|

---