Method of producing amides, their diastereomers, racemates or their acid-additive salts

专利摘要:
The invention relates to acid amides, in particular the preparation of compounds of the general formula I: @ X- (CH 2 ) N - (CHR) M -C (O) -NR 1 R 2 , where A and B are the same or different nitrogen, CH V and WH, halogen, C 1 -C 3 -alkyl, C 1 -C 3 -alkoxy, CF 3 Z (is in ortho or para position with respect to B) - phenyl, thienyl, pyridyl or phenyl, substituted with mono- or di-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, CF 3 , NO 2 , CL the group -X- (CH 2 ) N - (CHR) M -C (O) -NR 1 R 2 is in the ortho-position or the para-position with respect to B RH, C 1 -C 3 -alkyl R 1 and R 2 are the same or different n or branched C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, phenyl, C 3 -C 6 alkenyl, provided that the double bond is not in position 1 , 2 to the nitrogen atom, or NR 1 R 2 - cycle of piperidine, pyrrolidine, morpholine or thiomorpholine X-CHR 3 with R 3 -C 1 -C 3 -alkyl, H and M = 0 or 1, N = 0-2, or X = * 980 or * 98S and M = 1, N = 0-2, for with the exception of substances, where A = B is N, and Z is in the para position to B, and X-CHR 3 , when A is CH and B is N, and Z is in the ortho position to B, X is * 980, R is H and (M + N) = 0-3, or their dysterioisomers, racemates or additive salts, suitable for the treatment of immunosuppressive conditions. Synthesis of lead compounds of the formula I, where together NR 1 R 2 is the E group - C 1 -C 4 -alkoxy- or C 1 -C 4 -alkoxycarbonyloxy group, and the amine of the formula II: NHR 1 R 2 followed by isolation or separation of enantiomers or transfer to the desired salt. New substances of low toxicity (LD 50 = 200 mg / kg). 1 tab.
公开号:SU1614759A3
申请号:SU874202412
申请日:1987-04-06
公开日:1990-12-15
发明作者:Бенавид Хесус；Дюбрек Мари-Кристин；Ле Фюр Жерар；Рено Кристиан
申请人:Рон-Пуленк Санте (Фирма)；
IPC主号:

专利说明:

The purpose of the invention is the development of an accessible method for obtaining compounds of the formula I, which have high anxiolytic, anticonvulsant properties,
The invention is illustrated by the following examples.
Example 1. A mixture of 4.3 g of 2-feIl-4-quinazoline propionate and 30 cm of dietstamine is heated at 250 ° C for 40 hours. After cooling, the excess diethylamine is evaporated. The residue is subjected to x-chromatography on silica gel using a mixture of cyclohexane-ethyl acetate (1: 2 by volume) taken as eluant. 3.2 g of the compound is recovered, which
recrystallized in a simple opyl ether. 2.2 g of N, N-diethyl-2 - phenyl-4-quinazoline propanamide, melted, are obtained.
Q
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The NMR spectrum of the proton in chloroform containing deuterium shows the following characteristics:
1.2 ppm;
4.2rrga; ;
3.3 rrt;
5.7ррт;
2.8ррт;
7.9%; 7.3 pps; 6.7 rrga.
To 2.21 g of 3- (2-aminobenzox1) pro-pionate / ethyl and 4.2 cm of triethylamine in 25 cm of chloroform, 2.81 cm of 3-methoxybenzoyl chloride was added at 5 C. The mixture is left for 1 hour at ambient temperature (about 20 ° C), then 25 cm of water is added and the organic phase is decanted under reduced pressure, and the residue is dissolved in 17 g of acetate
five
ammonium. The mixture is kept for 7 hours, after which the acetic acid formed is evaporated under reduced pressure. The residue is poured onto 100 cm of water and the water is extracted three times with 50 cm of ethyl acetate. The aqueous phase is then dried, s.with magnesium sulfate, filtered and evaporated to dryness under reduced pressure. The resulting product is chromatographed on silica gel using a mixture of cyclohexane-ethyl acetate (1: 1 by volume), taken as eluant. After recrystallization in ethanol, 1.5 g of 2- (3-methoxyphene 1.x) -A-quinazoline ethyl propionate, melted at 7CNW, is obtained
Example 3. The effects are similar to those described in Example 1, however 4.2 g of 1-phenyl-3-isoquinoline ethyl propionate and 20 cm of diethylamine are used. After the first chromatography on silica gel using a mixture of cyclohexane-ethyl acetate (1: 1 by volume) as eluant, a second chromatography carried out with eluant with ethyl acetate, and crystallization carried out in petroleum ether, 0.6 g N, N -diethyl-1-phenyl-3-iso-quinolinpropanamide, melt plow at 70 C.
1-Phenyl-3-isoquinoline ethyl propionate receive according to the following technology.
A mixture of 20 g of 3-methyl-1-phenyl-isoquinoline, 17.8 g of N-bromosuccinimide and 0.2 g of benzoyl peroxide in 685 cm of carbon tetrachloride is maintained at boiling for 20 hours. Filtration and evaporation of the filtrate is carried out under reduced pressure. The residue is chromatographed on silica gel using a mixture of cyclohexane-ethyl acetate (9: 1 by volume), taken as eluant. 8.7 g of 3-bromo-methyl-1-phenylisoquinoline are recovered, melting at 109 ° C.
To 3.36 g of 80% sodium hydride in oil and 80 cm of anhydrous tetrahydrofuran a solution of 17.9 g of diethyl malonate in 100 cm of anhydrous tetrahydrofuran is added dropwise under an atmosphere of nitrogen. After stirring for 1 hour, a solution of 8.3 g of 3-bromomethyl-1-phenylisoquinoline in 100 cm of tetrahydrofuran is added dropwise and left, stirring, at ambient temperature (approximately) for one hour. Then add 200 cm of water and extract the aqueous
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phase three times 200 cm of ethyl acetate. The organic phase is dried over magnesium sulphate, the filter is one and evaporated to dryness under reduced pressure. The residue is chromatographed on silica gel using a mixture of cyclohexane-ethyl acetate (4: 1 by volume), taken as eluant. 9.6 g of oil is recovered, which is dissolved in 95 cm of concentrated hydrochloric acid, and kept at boiling for 20 hours. After cooling, 200 cm of water are added, the aqueous phase is washed twice with 50 cm of ethyl acetate, lye (potassium hydroxide) is added to pH 5 and extracted three times with 50 cm of chloroform. The organic phase is dried over magnesium sulphate and evaporated to dryness under reduced pressure. 2.9 g are obtained: 1-phenyl-3-isoquinoline propanoic acid, melting at.
2 g of 1-phenyl-3-isoquinoline-propanoic acid and 2 cm of concentrated sulfuric acid in 20 cm of absolute ethanol are stirred for 20 hours at ambient temperature (approximately). The mixture is dissolved in 100 cm of water, alkalinized to pH 9 with a concentrated solution of ammonium hydroxide and extracted three times with 50 cm3 of methylene chloride. The organic phase is suta on magnesium sulphate, filtered and evaporated to dryness under reduced pressure. 1.9 g of 1-phenyl-3-isoquinoline-ethylpropionate are obtained in the form of an oil having a trace of the NMR spectrum of the proton in chloroform containing deuterium :. Hg
Other H aromatic, Ag-CH, S.
sn-sn G
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sn
B
3
Example 4. The actions are similar to those described in Example 1, however, 50 use 6.1 g of 3-phenyl-1-isoquinoline ethyl propionate and 30 cm of diethylamine. The crude product is subjected
purification, carried out sequentially (4 times) chromatography on silica gel 55 and using a mixture of cyclohexane-ethyl acetate (7: 3 by volume) as eluant. This gives 1.4 g of H, N-diethyl-3-phenyl-1-isoquinoline-p-pamide, melting at 58 (:.,
3-Phenyl-1 isoquinolyl ethyl propionate is obtained by following the yyr-iM method.
A mixture of 21 g of 1-methyl-3-phenyl-: isoquinoline, 30.6 g of M-bromosuccini | type | and 1 g of benzoyl peroxide in 730 cm of carbon tetrachloride is maintained at boiling for 48 hours; after cooling, the mixture is filtered and evaporated | Nyy filtrate to dryness under reduced pressure. The residue is chromatographed on silica gel using toluene-methanol (98; 2 by volume) as eluant. After 1 installation in pro-ICTOM isopropyl ether,
11 g of 1-bromoethyl-3-phenylisoquinoline; melted at
6.5 g of an 80% sodium hydride in oil is placed in an atmosphere of nitrogen, because it is tetrahydrofuran, then a solution of 34.9 g of di-ethyl malonate in 200 cm of anhydrous tetrahydrofurano is added in Icaps. After stirring for 1 hour at ambient temperature. | medium. (approximately) add plant-: thief 16.2 g of 1-bromomethyl-3-phenyliso-: noline in 200 cm of anhydrous tetrahydrofuran. After stirring for 20 hours at 200C, 200 cm of water is added and: the aqueous phase is extracted with ethyl acetate. The organic phase is dried and evaporated to dryness under reduced pressure. The residue is chromatographed on silica gel using a mixture of cyclohexane-ethyl acetate (8; 2 by volume) as eluant. 11.5 g of compound are recovered, which are dissolved by IB 115 cm of concentrated hydrochloric acid, and then kept at boiling for I h for 20 hours. 200 cm of water are added, the precipitate is filtered, and the mixture is filtered. wash it with water and acetone. 6.7 g of 3-phenyl-1-isoquinoline propanoic acid are obtained, melting at.
.one"
For 20 hours at 20 ° C, stir
6.7 g of 3-phenyl-1-isoquinoline-propanoic acid and 7 cm of sulfuric acid in 70 cm of ethanol are used. The resulting solution is poured into 400 cm of water, the aqueous phase is made alkaline with a concentrated solution of ammonium hydroxide. Thrice realized Extraction is carried out with 100 cm of methylene chloride, then the organic phase is dried and evaporated to dryness under reduced pressure. 6.3 g of 3-phenyl-1-isoquinoline propionate ethyl, melting at, is obtained.
-
Q g
0 5 PLN
45
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Example 5 The actions are similar to those described in Example 1, however, 3 g of 2-fe; 1 Id-4-quinodine ethyl acetate and 60 cm of diethylamine are used.
The residue is chromatographed on silica gel using cyclohexane-ethyl acetate (50:50 by volume) as eluant. After recrystallization in ethyl acetate, 2.05 g of N, N-diethyl-2-phenyl-4-quinoline acetamide was isolated, melting at 86 ° C.
2-Phenyl-4-quinoline ethyl acetate is obtained by the following method) 1 method.
Under a nitrogen atmosphere, 12.9 cm of diisopropylamine are added to 40 cm of dry tetrahydrofuran. The solution is stirred, then cooled to minus. 46 cm of a 1.6 M solution of butyl lithium in hexane are introduced over 15 minutes. After the temperature has stabilized, minus 8.1 g of 2-phenyllepidine in 20 cm of tetrahydrofuran is introduced into the minus for 15 minutes, then the ambient temperature is restored (approximately 20 ° C). About the half-added solution is added dropwise under nitrogen to solution 9 cm. of distilled carbonate in 50 cm of tetrahydrofuran, pre-cooled to minus 20 ° C. After the introduction of the above solution, the mixture is left stirring at ambient temperature (about 20 ° C) for one hour.
Then 25 cm of absolute ethanol is added dropwise, then 10 cm of glacial acetic acid and finally 100 cm of water. The tetrahydrofuran is evaporated under reduced pressure, and the aqueous phase is dissolved in 200 cm of ethyl ether. The ether phase is washed with water, dried over magnesium sulphate and evaporated under reduced pressure. The remainder; dissolved in 100 cm of toluene, and then again evaporated to remove acetic acid,
one .
The residue is chromatographed on silica gel using cyclohexane-ethyl acetate (90:10; v / v) as eluant. 7 g of 2-phenyl-4-quinoline ethyl acetate are obtained as a yellow oil. This product can be dissolved in acetone and, after adding a solution of hydrochloric acid in ethyl ether, 5.13 g of 2-phenyl-4-quinoline ethyl acetate hydrochloride is isolated, melting at
9 -16U759
Example 6. Under nitrogen atmosphere, add 3 g of carbonyldiimidazole to a suspension of 2.67 j txL-methyl-2-phenyl-4-quinazoline propanoic acid in 30 cm of anhydrous tetrahydrofuran.
.3
For 2 hours of stirring, add 6 cm of dethylamine and stir for a further A hour. Add 150 cm of water and 10 cm of ethyl acetate. The mixture is decanted, the aqueous phase is extracted twice with 100 cm of ethyl acetate, the organic phase is dried on magnesium sulfate and evaporated to dryness. The residue is chromatographed on silica gel using cyclohexane-ethyl acetate (1: 1 by volume) for the first time, and the second is cyclohexane-ethyl acetate (8: 2 by volume) o
After recrystallization in isopropyl ether, 1 g of K, N-diethyl-k; - methyl-2-phenyl-4-quinoline-propanamide, melting at.
0-Methyl-2-phenyl-4-quinoline propanoic acid was prepared as follows. I
A mixture of 15 g of 4-methyl-2-phenylquinazoline, 13.3 g of N-bromosuccinimide and 1.65 g of benzoyl peroxide in 150 cm of carbon tetrachloride is maintained for 3 hours at 90 ° C, filtered, the filtrate is evaporated and the residue is chromatographed on silica gel using a mixture of cyclohexane-ethyl acetate (9: 1 by volume) as eluant. 11 g of 4-bromomethyl-2-phenylquinosoline are obtained, melting at 110 ° C.
To 4 g of 80% sodium hydride in oil and 60 cm of anhydrous tetrahydrofuran under a nitrogen atmosphere is added a solution of 23 g of diethylmethylmalonate 100 cm of anhydrous tetrahydrofuran. After stirring for asa, a solution of 9.9 g of 4-bromo-methyl-2-phenylquinoline is added to 100 cm of a-one tetrahydrofuran and stirred for another 2 hours at ambient temperature (about 20 ° C). Add 100 cm of water and extract three times 100 cm of ethyl acetate. The organic base is dried on magnesium sulfate, then evaporated to dryness under reduced pressure. The residue is dissolved in 100 cm of concentrated hydrochloric acid with 100 cm of acetic acid, the whole mixture is extruded at 110 ° C for 4 hours. After cooling, the precipitate is filtered off, washed first with war and then with simple nsopropyl
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s c n p p p ra no no p a r p o p s p o p s p y
we are 1, ki and
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25
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 ABOUT
by ether. After drying, 4 g of Oo-methyl-2-phenyl-4-chiNazolinpro, 0 are obtained.
Panovoy acid, melting at 180 C. Example 7. The effects are analogous to those specified in Example 6, however, 1.95 g of 2-phenyl-4-quinazoline-propanoic acid, 1.36 g of carbonyldiimo 10 are used as starting compounds.
at
five
Dazole and 3 cm of N-methylaniline 40 cm of anhydrous tetrahydrofuran. After purification by chromatography on silica gel using ethyl acetate as eluant and subsequent recrystallization in a mixture of ethyl acetate and isopropyl ether (1: 5 by volume), 0.63 g of N-methyl-N-phenyl are obtained. -2- (J) Enil-4-xinazo olipopanamide, melted at 116 ° G. 2-Phenyl-4-quinazolipropanoic acid was prepared as follows.
5.4 g of 80% sodium hydride in oil with 250 cm of anhydrous tetrahydrofuran are placed in an atmosphere of nitrogen, then, after cooling the mixture to 5 ° C, 25.6 g of diethyl malonate are added to it. When the evolution of hydrogen ceases, a solution of 23.9 g of 4-bromomethyl-2-phenylquinazoline in 100 cm of anhydrous tetrahydrofuran is added to the mixture. After stirring for an hour at ambient temperature (about 20 ° C), 25 cm of acetic acid is added, then the solvent is evaporated under reduced pressure, and the residue is dissolved in 150 cm of concentrated hydrochloric acid and 150 cm of acetic acid. The whole mixture is kept at 120 C for 15 hours, then evaporated again, 200 cm of water, 150 cm of ethyl ether are added and the mixture is basified to pH 11 using sodium hydroxide. The organic phase is decanted, the aqueous solution is washed twice with 100 cm of ethyl ether. The pH of the aqueous phase is adjusted to 4 and extracted twice with 10 ml of ethyl acetate. The organic phase is dried over magnesium sulfate and evaporated to dryness under reduced pressure. The residue is recrystallized in ethyl acetate. 9 g of 2-phenyl-4-quinazoline propanoic acid is obtained, melting at
Example 8, The actions are similar to those described in Example 6, however, 1.95 g of 2-phenyl-4-schnazoline propanoic acid, 1.36 g of carbonyldindimol and 1.38 cm of piperidine in 40 cm of tetra-
1116
mr; rofu1-1a. After :: |) isomatoglphine, wasp 1 1 paired silica gel using (;: ethyl acetate as eluent, and recrystallization of a mixture of these g); - acetate: simple isopropyl firm 4: 2 each year) get 0.88 1 - 1 | - / 2-phenyl-A-quinazolium / -propionylT-Piperidine, melted at 115 ° C.
Example 9. The action is similar- 1 | s described in Example 6, however
2.17 g of 2- (2-chlorophenyl) -4-quina-olanopropanoic acid, 1.35 g of carotildiimide ash and 1.5 cm of diethylamine per 20 cm of tetrahydrofuran are used as starting materials.
li
; After chromatography on silica gel using eluant, ethyl acetate and 1 crystallisation. In isopropyl ether, 1.5 g of N, N-diethyl-1- / 2-chlorophenyl / -4-dipazolin-propanamium are obtained. a, melting shake at.
2- / 2-Chlorophenyl / -4-quinicpropane-ftonyio acid obtained from the following isobomy.
To a solution of 3.3 g of 3- (2-aminbenzoyl) / propionate of ethyl and 6.3 cm of triethyl amine in 35 cm of chloroform are added at 5 C with 3.2 cm of orthochlorobenzoyl chloride. For 20 hours, stir in a stump at ambient temperature (about 2 ° C), then the solvent is removed by evaporation under reduced pressure. The residue is dissolved in 50 cm of simple ethyl ether, the insoluble is filtered off, and the filtrate is evaporated. The remaining substance is mixed with 15 g of ammonium acetate and maintained at 110 ° C for 4 hours. After cooling, 100 cm of water are added and the aqueous phase is extracted three times with 50 cm of chloroform. The solvent is removed under reduced pressure, and the residue is dissolved in 50 cm of ethanol and 10 cm of a concentrated solution of sodium hydroxide. The solution is kept for one hour, the ethanol is evaporated, 100 cm of water are added, the aqueous phase is washed with 50 cm of ethyl ether three times. The aqueous phase is acidified to pH 1 and. Extractively extracted with 100 cm of ethyl ether. The organic phase is dried over magnesium sulphate, filtered and then evaporated to dryness under reduced pressure.
73912
4.8 g of a substance is recovered, which is recrystallized in ethanol, 2.2 g of 2- / 2-: lorofen / -4 - quinazoline-propanoic acid, melting at 5,175 ° C, are isolated.
Example 10 “Acting; 1 is logical as described in Example 6; however, 1.35 g of 2- (4-nitrophenyl) -4-quinazolin-propanoic acid, 0.82 g of carbonyldiimidazole and 0, are used as starting materials. 9 cm diethylamine in 20 anhydrous tetrahydrofuran. After chromatography on silica gel using ethyl acetate as eluant and recrystallization into ethyl acetate. 0.35 g of S, N-dieth-1- 2- / 4-nitrophenyl / -4-quinazolinopropanamide is obtained, - melted at 20,
2- / 4-Nitrophenyl / -2-quinazoline propanoic acid was prepared as follows.
A mixture of 3.34 g of para-nitrobenzoic acid and 20 cm of thionyl; Excess thionyl chloride is removed by evaporation under reduced pressure, then to the remaining material.
30 were added 20 cm of chloroform, 5.5 cm of triethylamine and 2.21 g of 3- [2-aminobenzoyl] methyl propionate. Stirring is carried out at ambient temperature (about 20 ° C) for 2 hours. The solvent is removed under reduced pressure, the residue is dissolved in 50 sk of ethyl acetate, filtered and the filtrate is concentrated to dryness. The remaining material was combined with 20 g of acetamide and ammonium, and the resulting mixture was incubated for 6 hours at 150 ° C. After cooling, 250 cm of water was added and the mixture was extracted four times with 100 cm of ethyl acetate. Organic
The 45 phase is washed twice with 100 cm of a normal solution of sodium hydroxide and 50 cm of water. The organic phase is dried on magnesium sulphate, filtered and evaporated to dryness under reduced
50 pressure Obtain 2.8 g of substance, which is combined with 50 cm of ethanol and 2.5 cm of a concentrated solution of sodium hydroxide. After 30 minutes at ambient temperature
55 of the medium, ethanol is removed by evaporation under reduced pressure and 200 cm of water are added. The aqueous phase is washed three times with 50. cm of ethyl ether, then acidified.
to pH 1 and the precipitate is filtered off. After washing with water in methylene chloride and drying, 1.4 g of 2- (4-nitrophenyl) -4-quinazoline-propanoic acid are obtained, the spectrum of which 1NP by proton in deuterium-containing dimethyl sulfoxide has the following characteristics:
3.7 ppm; 3 ppm;
2
A: 8.9 ppm;
7,7-8,4 rrga
Ag-CH 8
-sn -soon, 8
H aromatic in the meta position with respect to NOg, o: 8.4 ppm; H aromatic in the ortho position with respect to N0 Other H aromatic
Example 11. The effects are similar to those described in Example 6, however, 1.32 g of 2- (4-methylphenyl) -4-quinazoline propanoic acid, 0.88 g of carbonyldiimidazole and 0.95 cm of diethyl amine 20 see anhydrous tetrahydro furan ..
After chromatography on silica gel using ethyl acetate as eluant, and recrystallization in aqueous 50% ethanol, 0.75 g of N, N-diethyl-2- (4-methylphenyl) -4-quinazoline propanamide, at 80 ° C.
2- / 4-Methylphenyl / -4-quinazolinprop. New acid is obtained in the following way
During 4 hours a mixture of 2.72 g of 4-methylbenzoic acid and 20 cm of thionyl chloride is boiled at boiling point. The excess thionyl chloride is removed by evaporation under reduced pressure, and 2.21 g of 3- [2-aminobenzoyl] -propionate ethyl, 20 cm of toluene and 5.5 cm of trisylamine are added to the residue. The mixture is stirred for one hour at ambient temperature (about), filtered, the filtrate is evaporated under reduced pressure. To the remaining substance is added 20 g of acetic acid.
ammonium and maintain the mixture for 7 hours at 110 ° C. After cooling, add 100 cm of water and extract the aqueous phase three times with 100 cm of ethyl acetate. The solvent is evaporated under reduced pressure and 20 ethanol and 3 cm of a concentrated sodium hydroxide solution are added to the residue. The mixture is kept for ca.

th
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at 80 ° C, then the ethanol is evaporated under reduced pressure, 100 cm of water are added and the aqueous phase washed three times with 100 cm-ethyl ether is acidified to pH 1, the solid is extracted three times with 100 cm of ethyladylate. The organic phase is dried over magnesium sulphate, filtered and evaporated to dryness under p-glass pressure. 3.1 g of compound are obtained, which is recrystallized in absolute ethanol, 1.5 g of 2- (4-methylfe-H11l) -4-quinazoline propanoic acid are obtained, melting at 180 С „
Example 12 The actions are similar to those described in npi-iMepe 6, however, 1.34 g of 2- / 2-pyridyl / -4-quinazoline propanoic acid, 0.93 g of carbonyldit-chichadazole and 1 cm of diethsamine are used as starting products. 25 cm dimethylformamide. After chromatography on silica gel using chloroform-methanol (95: 5 by volume) as eluant and crystallization in ethyl acetate, 0.58 g N, H-diethyl-2/2-pyridyl / -4-quinazoline-propanamide, melting at
2- / 2- Pyridyl / -4-quinazolinpropano- in}, the acid is obtained in the following way.
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2.46 g of 2-pyridylcarboxylic acid and 15 cm of dry dimethylformamide are placed in a nitrogen atmosphere. 3.89 g of carbonyldiimidazole is added, the mixture is stirred for 20 minutes, and a solution of 2.21 g of 3- (2-amine) ethanol / propionate ethyl in 10 cm of dry dimethylformamide is added. The mixture is incubated for 20 hours at PO ° C, the solvent is evaporated under reduced pressure. 50 cm of water are added and extraction is carried out four times with 50 cm of ethyl ether.
The organic phase is dried over magnesium sulphate and then evaporated to dryness under reduced pressure. 3.17 g of crude material are obtained, which is recrystallized in absolute ethanol. 1.7 g of 3 -2- (2-pyridylcarboxamide) -benzoyl-propionate-ethyl are obtained, which are brought into contact with 10 g of ammonium acetate and 5 cm of acetic acid. The mixture was incubated for 10 hours at 110 ° C. After cooling, 100 cm of water are added and the aqueous 1 phase is extracted three times with 50 cm of ethyl acetate, the solvent is evaporated at a pony pressure and more than 15
The substance is dissolved in 20 cm of ethanol and 2 cm of concentrated sodium hydroxide. The resulting substance: is kept for an hour, evaporates the ethanol, then 25 water and acetic acid about pH 4 are added. The precipitate is filtered, washed with water, methylene chloride and sunt. This gives 0.82 g of 2- (2-pyridyl) - quinazoline propanoic acid, the 1 MR spectrum of which, according to the proton in deuterium-containing chloroform and deuterium-containing dimethyl sulfoxide, has the following characteristics: 3.7 ppm; .
1614759
I pyridyl
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s
8.9 ppm; 3 ppm; 7.5 ppm;
1-C.N2 - SSYuN,
5-pyridyl
Other H aromatic from 7.6 to 8.3 ppm;
Example 13. The effects are analogous to those described in Example 6, however: from the quality of the starting products, 8 g of oi-methyl-3-phenyl-1-isoquinopenanoic acid, t, 62 g of carbonyldiimdazole and 5 cm of diethylamine B 25 cm are used. tetrahydrofuran.
After three-fold chromatography on silica gel using a mixture of cyclohexane-ethyl acetate (7: 3 v / v) as eluant and crystallization in isopropyl ether, 1.3 g of K, M-dimethyl-o-methyl-3-phenyl-1- are obtained. isoquinolinpropanamide, melted at 57 ° C,
 0-Methyl-3-phenyl-1-isoquinoline propanoic acid was prepared as follows.
2.1 g of 60% sodium hydride in oil and 50 cm of anhydrous tetrahydrofurano are placed in a nitrogen atmosphere. A solution of 9.1 g of methyl malonate diethyl in 50 cm of anhydrous tetrahydrofuran is then added dropwise. Stirring is carried out for one hour at ambient temperature (about), then a solution of 10.4 g of 1-bromomethyl-3-phenylisoquinoline in 100 cm of anhydrous tetrahydrofuran is added. After 20 hours of contacting the above reagents, 200 cm of water are added and the aqueous phase is extracted three times with 50 cm of ethyl acetate. After removing the solvents under reduced pressure, 19 g of the substance is recovered, which is maintained at boiling for 20 hours in 70 cm of concentrated hydrochloric acid and 70 cm
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25 20 VA OK OK
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acetic acid. After oh; a mixture is poured into 1000 cm of water, the solution is alkalinized to pH 10 with lye (sodium hydroxide), the aqueous phase npo-j is washed with 100 cm of ethyl acetate, acidified with hydrochloric acid and extracted three times with 200 cm of chloroform. The organic phase is dried on magnesium sulfate, filtered, and evaporated to dryness under reduced pressure. 7.4 g of oi-methyl-3-phenyl-1-isoquinoline propanoic acid are obtained, melting at 184 ° C.
Example 14. For 90 minutes, 3 g of 2-phenyl-4-quinolinepropanoic acid in 9 cm of thionyl chloride is heated under reflux. Thionyl chloride is evaporated, the residue is dissolved in 100 cm of toluene and again evaporated. 60 cm of dry toluene are then added to the residue and dropwise added with stirring.
20 minutes see diethylamine. Stir for one hour at ambient temperature (about 20 ° C) and then dissolve in 60 cm of water. The organic phase is decanted. The aqueous phase is extracted twice with 30 cm of toluene, the organic phases are combined,
dried over magnesium sulfate and evaporated under reduced pressure
The residue obtained is dissolved in acetone and, after addition of a solution of 35 hydrochloric acid in ethyl ether, 2.3 g of M, M-diethyl-2-phenyl-4-quinoline-propanamide chlorohydrate, melting at 126 ° C, are isolated.
Example 15. During reflux, 5 g of 2-phenyl-4-quinolinepropanoic acid and 1.43 of thionyl chloride are heated in 250 cm of chloroform overnight. Then act according to example 15, one 40
45
use 5.3 cm of piperidine.
The residue is stirred for one hour with 60 g of silica gel in 100 cm of ethyl acetate. The silica is removed by filtration and washed 7 times with 10 cm of ethyl acetate. The organic phases are combined and evaporated at an increased pressure. After recrystallization of the residue in ethyl acetate, 2 g of 1- 3- [2-phenyl-4-quinoline] -propionyl D-piperidine, melting at 110 ° C, are obtained.
Example 16. The actions are similar to those described in Example 15, however, as a starting material, use
3 g of 2-feiyl-4-cnnolinpropanoic acid, 0.9 cm of thionyl chloride in 150 cm of chloroform and 2.78 cm of morpholine are added.
The residue is stirred for one hour with 35 g of silica gel in 70 cm of ethyl acetate. Silicon dioxide is removed by filtration and 7-fold washing with 10 cm of ethyladetate. The organic phases are combined and evaporated under reduced pressure. After recrystallization of the residue in ethyl acetate in the presence of animal charcoal, 1.5 g are obtained 4- | 3- [2-phenyl-4-quinolyl] -propionyl | - morpholine, melted at.
Example 17. The actions are similar to those described in Example 15, but using 3 g of 2-phenyl-4-quinoline propanoic acid, 2.3 cm of thionyl chloride in 150 cm of chloroform and 4.4 cm of dipropylamine as the starting materials. The residue is stirred for one hour with 40 g of silica gel in 80 cm of ethyl acetate. The silica is removed by filtration and then washed 7 times with 10 cm of ethyl acetate. The organic phases are combined and evaporated under reduced pressure.
The residue obtained is dissolved in acetone and after the hydrochloric acid solution is added to ethyl ether, 2.41 g of K hydrochloride is isolated, K-dipropyl-2-phenyl-4-quinoline-propanamide melting at 130 ° C. Example 18 The actions are similar to those described in Example 15, but 3 g of 2-phenyl-4-quinoline propanoic acid, 2.3 cm of thionyl chloride, 150 cm of chloroform and 2.7 cm of pyrrolidine are used as starting materials. The residue is stirred for 2 hours with 36 g of silica gel in 80 cm of tillacetate. Silicon dioxide is removed by filtering, followed by washing once with 10 cm of ethyl acetate. The organic phases are collected and concentrated under reduced pressure. After the residue has been fixed in ethyl acetate, 2 g of 1- 3- (2-phenyl-4-quinolyl) - ropionyl-pyrrolidine is melted, melting at 116 ° C
Example 19. Operate according to the prior 15, using 3 g as the starting material (y; -methyl-2-phenyl-quinoline-pryphoic acid in 30 cm of loroform, 0.97 cm of thionyl chloride, 3.2 cm of diethylenamine in 5 cm of chloroform, reducing to 30 min. Time for obtaining acid chloride. Residue
in p ki go
10 woo about
hee
J5 45 45 neither
20 4 wah ta che
25 ti
by us Or 30 50
Ef yut Ma yes 35 in for yes 45 pl
40 4na l 45 60 units thief 220 to t 50 hlo. tet dut okr sa 55 saus wed
was isolated and dissolved in ethanol, and after adding a solution of hydrochloric acid in ethyl ether and recrystallization in a mixture of ethanol and ethyl ether (1: 3 by volume, O, 2.9 g of hydrochloride K, N-diethyl-o6-m-ethyl- 2-phenyl-4-quinolish1panamide, melted at 16l Co
10 oC-Methyl-2-phenyl-4-quinoline propanoic acid can be obtained as follows.
I. Preparation of 4-chloromethyl-2-phenyl-quinoline.
J5 To cooled to a suspension of 45 g of 2-phenyl-4-quinoline methanol c. 450 cm of chloroform are added over 45 min. 35 cm of thionyl chloride, followed by stirring for
20 4 hours at ambient temperature (about 20 ° C). The solvent is evaporated under reduced pressure and the residue is dissolved in toluene, after which toluene is evaporated to remove
25 thionyl chloride
The residue is dissolved in 1000 cm of water, alkalinized to pH 9 with concentrated ammonium hydroxide solution. The organic phase is extracted three times with 0 500 cm of ethyl ether,
ether, the th phase is washed three times with 200 cm of water, dried over magnesium sulfate and evaporated under reduced pressure. The oil-like residue is diluted with isoproxy ether, then the ether is evaporated off under reduced pressure. 45.3 g of 4-chloromethyl-2-fensh1quinoline are thus obtained, melting at 79 ° C.
0 ii. Preparation of o-methyl-2-feiyl-4x11Noline propionic acid.
Under a nitrogen atmosphere, 14.3 g of sodium hydride are slowly added to 220 cm of dry tetrahydrofuran in the form of 5 60% dispersion in oil. A solution of 62.5 g of diethylmethylmalonate in 220 cm of tetrahydrofuran is then added slowly over 2 hours, after during one hour, a solution of 45.3 g of 4-0 chloromethyl-2 - (}} enylquinoline in 400 cm of tetrahydrofuran. Stirring is carried out for 2 hours at ambient temperature (about 20 ° C), then the mixture is heated for about - 5 ° C with reflux. The temperature of the mixture is brought to ambient temperature (about 20 ° C), then dropwise Bavlov dissolved 22 cm of glacial acetic acid and then 500 cNr
Tetrahydrofur is removed by evaporation under reduced pressure; the remaining reaction mixture is diluted with 500 cm of water, extracted three times with 400 cm of ethyl ether: | i. The ether dressing phase is washed with water and concentrated under reduced pressure.
The resulting residue is dissolved with 500 cm of a concentrated solution of hydrochloric acid and 500 cm of glacial acetic acid. Heating is carried out for 30 minutes under reflux. The acids are maximally evaporated under reduced pressure, and the residue is dissolved in 1000 cm of water, then the solution is alkalinized to pH 10 with a concentrated solution of ammonium hydroxide, 300 cm of ethyl ether are added and left under stirring for 15 minutes. This phase is decanted, washed twice with 200 cm of water. The aqueous phase is twice a day; | i; bi is washed with 300 cm of ethyl ether. The aqueous phases are collected, acidified with stirring to pH 4-5 with glacial acetic acid, stirred for another hour, after which the precipitate is obtained from iHsiKT and 47.6 g are obtained with | 4-methyl-2-phenyl-4-quinolinepropanoyl Acids by melting at 181 ° C.
Example 20. Operate according to Example 19, using 3 g of oC-methyl-2-phenyl-4-quinolinpropanoic acid, Non-rotating in 30 cm of chloroform, 0.97 cm of thionyl chloride and 3.2 cm of diethylamine in 5 cm of chloroform.
The residue is isolated, dissolved in ethanol and after adding a solution of hydrochloric acid in ethyl ether, recrystallization in ethanol-ethyl ether (1: 3 volume) and two subsequent recrystallization in ethanol-ethyl ether (1: 2). 2 g of hydrochloride K, K-diethyl-0-methyl-2-phenyl-4-quinolinepropanamide left
175 С
rotating, melting
in EtOH at 21 with djy
With 0.5% -85.5 ± 2 ° „
oi-Methyl-2-phenyl-4-quinoline propanoic levogyrate acid can be obtained by separating about -methyl-2-phenyl-4-quinoline propanoic racemic acid as follows
1 „Preparation of N- / 1-phenyl-.2-hydroxy-ethyl / v; -methyl-2-phenyl-4-quinolinepro-papamides of diasteromers.
five
0
five
42.5 g of oi-methyl-2-phenyl-4-quinoline-propane ct slot and 13.8 cm of thionyl chloride in 450 cm of chloroform are heated under reflux for an hour for an hour. The solvent is evaporated under reduced pressure, the residue is dissolved in chloroform, which is again evaporated,
To a stirred solution of 20 g (-) (x1-phenylglycinol in 200 cm of chloroform was added 41 cm of triethylamine, after which a solution of the acid chloride obtained above taken in 400 cm of chloroform was added over 1.5 h. The mixture was stirred for 2 hours at ambient temperature (approximately), then chloroform is evaporated under reduced pressure, the residue is dissolved in 500 cm of water and 300 cm of ethyl acetate; The organic phase is decanted, the aqueous phase is extracted with 100 cm of ethyl acetate. The organic phases are collected, washed with water, dried magnesium sulfate and evaporated under reduced pressure. 10 g of the product, the residue is chromatographed on silica gel using as elyu- anta chloroform-ethyl acetate (50:50 by volume) of
In this way 4.6 g of N- (1-phenyl-2-hydroxyethyl) -o6-methyl-2-phenyl-4-quinoline propanamide, Form A, melted at 134 ° C, which is first washed, and 4.6 g are obtained. H- / 1-fshsh-2-hydroxyethyl / b (; - methyl-2-phenyl-4-xiylinopropane rada, 35 form Bj. Which is washed out after form A and which has a melting point of 158 C.
Ii. Preparation of od -methyl-2-phenyl-4-quinoline propanoic levorotatory acid
5.5 g of N-1 / -phenyl-2-hydroxyethyl / 0-methyl-2-fench-1-4-quinoline-propanamide (form A) are heated in reflux for 1.5 hours to 1.5 h in 27 cm of glacial acetic acid and 27 cm of concentrated hydrochloric acid solution.
The acids are evaporated under reduced pressure, the residue is dissolved in 120 cm of water, the solution is alkalinized to pH 10 with a concentrated solution of ammonium hydroxide, and the aqueous phase is washed with 250 cm of ethyl ether. The aqueous phase is acidified to pH 5 with crystalline acetic acid and extracted three times with 100 cm of ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate and concentrated under reduced pressure.
thirty
40
45
55
After recrystallization in ethanol, 2.6 g of o-methyl-2-phenyl-A-quinoline propanoic-levogravic acid, melting at 185 ° C, are obtained.
At 0.5% in glacial acetic acid, ot.p -37,7 + 2 at 22 ° С.
Example 21, Act as in Example 19, using as starting materials 3.4 g of oi-methyl-2-phenyl-4-quinoline-propanoic prodorotatory acid in 34 cm of chloroform, 1.1 cm of thionyl chloride and 3.6 cm of diethylamine in 5 cm of chloroform . The residue was dissolved, dissolved in ethanol and after the addition of hydrochloric acid solution in ethyl ether, recrystallization in ethanol-ethyl ether (1: 3 by volume) and subsequent recrystallization in ethanol-ethylether (1: 2 by volume) 2.55 g of hydrochloride, N, N-diethyl- (xJ-methyl-2-phenyl-4-quinolineproperamorbondrate, melted at 175 ° C) melted at 175 ° C.
at
.one.
At 0.5% in EtOH at 21 ° C sC + 81.6 + 2 °.
; o-Methyl-2-phenyl-4-quinolin-propanoic right-rotating acid can be obtained, like its left-rotating enantiomer in Example 20, using 6.6 g of N- / 1-phenyl-2-hydroxyethyl / -o6- as the source of the products methyl 2-phenyl-4-quinoline.opanamide-form B (Example 20) 33 cm of a concentrated hydrochloric acid solution and 33 cm of acetic acid.
The resulting residue is recrystallized in ethanol.
3.9 g of 6i-mo.til-2-phenyl-4-quinoline propanoic produsive acid are obtained, melting at.
At 0.5% in glacial acetic acid at 24 ° С Oil, + 33.3 ± 2 °.
Example 22. The procedure is carried out as in Example 19 using 2.03 g of o-methyl-2-phenyl-4-quinoline propanoic acid in 20 cm of chloroform as starting materials. 0.67 cm of thionyl chloride and 7 cm 3 M solution of dimethylamine in tolus le. The residue is dissolved in ethanol and after addition of a solution of hydrochloric acid in ethyl ether and recrystallization in a mixture of ethanol simple ethyl ether (1: 2 by volume)



1.4 g of hydrochloride M, N-dimethyl L-2-phenyl-4-quin ol ol ppanamide, melted at.

20
25
0
five
with reflux
Example 23 To a solution of 3.7 g of 2-fluor-4-quinol 1 Shbutanoic acid in 60 cm of chloroform, 1.02 cm of thionyl chloride was added, after which the mixture was heated for 15 minutes under reflux. The solvents are evaporated off under reduced pressure. The resulting residue is dissolved in 40 cm of chloroform. To this 10 solution, 6 cm of diethylamine is slowly added over 20 minutes. The mixture is stirred for 3 hours at ambient temperature (about 20 ° C), and then 40 cm of water is added. The organic phase is decanted, washed with 40 cm of water, cyuiaT on magnesium sulphate and evaporated under reduced pressure.
The residue is chromatographed on silica gel using cyclohexane-ethyl acetate (50:50 by volume) as eluant. Thus, 3.3 g of S, K-diethyl-2-phenyl-4-quinoline-butanamide are obtained, which are converted in acetone to monochlorohydrate, which is melted at.
2-Phenyl-4-quinolinbutanoic acid can be obtained as follows.
I. Preparation of J-oxo-2-phenyl-4-quinolinebutanoateethyl.
84 ml of a 20% potassium hydride suspension in oil are slowly added to 500 cNf of dry tetrahydrofuran under nitrogen. Then while stirring
5, 47 g of 2-phenylquinolin-2-carboxy-ethyl, and slowly over 2 hours at ambient temperature (about 20 ° C) —a solution of 24.4 g of ethyl succinate in 250 cm tetrahydrofuranium are introduced. After that, 80 cm of ethanol and 800 cm of water. The tetrahydrofuran is removed by injection, the aqueous phase is extracted twice with 200 cm of ethyl ether, the reaction mass is then acidified to pH 4.5 by adding glacial acetic acid to it and, finally, carried out three times. extraction 200. cm of ethyl ether. The ether-containing phase is washed with water, dried over magnesium sulphate and evaporated under reduced pressure.
The residue is dissolved in 600 cm 6 n. hydrochloric acid solution and heated
for 6 h. After
concentration under reduced pressure gives 57.4 g of a mixture containing 2-phenyl-4-quinoline carboxylic acid.
23t
 and Oxo-2-phenyl-4-quinolinbuta nsshuyu acid
The mixture is dissolved in 600 cm of absolute ethanol and 60 cm of concentrated Hdft of sulfuric acid, after which it is heated overnight with reflux "Ethanol is removed by evaporation under reduced pressure, and the residue is taken up in 600 cm of icy water and 220 cm of concentrated ammonium hydroxide solution. The aqueous phase is extracted three times with 700 cm of ethyl ether, and the organic phase is washed with water, dried on magnesium sulphate and evaporated under reduced pressure. The residue is chromatographed on silica gel using cyclohexane as an elute mixture en-ethyl acetate (90:10 by volume). Thus, a half of 24.4 g of J -oxo-2-phenyl-4-hino-L1 nbutanoatethyl is melted at bb C.
: Ii. Preparation of 2-phenyl-4-quinoline-, bz | tanoic acid.
I Heat 5 g of y-oxo-2-phenyl-4-quinoline bz tanoatethyl and 2.25 cm 98% for 15 minutes to 150 ° C for 15 minutes



Hydrazine hydrate in 15 cm diethylene glycol. The mixture is cooled to 12 ps, after it is introduced into it for 15 cm 2, 5 g of potassium hydroxide in the form of particles, and then heated to ps 12 hours.
: The reaction mixture is diluted with 300 cm of water, extracted three times
80
see ethyl ether. The ether was kept in phase, washed with 10 cm of water, the aqueous phase was collected, acidified to pH 4.6 by adding acetic acid and extracted three times with 100 cm of ethyl ether. Ether-Ss1g.oto phase is washed in water, dried on magnesium sulfate and evaporated at ps lower pressure. 3.7 g of 2-phenyl-4-quinolinbutanoic acid are obtained, Bp.
Example 24. Act as in Example 23, using, however, as starting materials, 1.7 g of o6-ethyl-2-phenyl-4-quinoline-butanoic acid chlorohydrate in 85 cm of chloroform, 0.38 cm of thionyl chloride and 2 , 2 cm diethylamine. After chromatography of the residue on silica gel using a mixture of cyclohexane-ethyl acetate (80:20 by volume) as eluant and crystallization in petroleum ether (40-60 ° C), 1.1 g of N, N-diethyl-fI 0 are obtained.
4759
five
0
five
24
ethyl 2-phenyl-4-quinolinbuta 1 amide, melted at.
0 (7 Ethyl-2-phenyl-4-quinolinebutanoic acid is obtained by hydrolysis of the corresponding ethyl ester using 6N hydrochloric acid.
B-Ethyl-2-phenyl-4-quinolinebutano-atethyl was prepared as follows.
To 30 cm of dry tetrahydrofuran, placed under a nitrogen atmosphere, add 2.96 cm of diisopropylamine. The solution is stirred and cooled to minus 70 s. Then, within 15 minutes, 11.3 cm of a 1.6 M solution of utility in hexane was introduced. After the temperature stabilizes at minus 70 ° C, a solution of 3.8 g of 2-phenyl-4-quinoline linbutanoatethyl in 30. cm tetrahydrofuran is introduced into the reaction mixture for 5 minutes. Stir for 30 MiiH at minus, after which it is introduced within 5 minutes of 1.15 cm of ethyl iodide and 0.8 cm of hexamethylphosphoramide in 20 cm of tetrahydrofuran. The mixture is stirred at 0
0
five
0
7 hours at minus 70 ° C. 7 cm of ethanol and then 2 cm of acetic acid are introduced into it. Leave
the mixture was allowed to adjust to ambient temperature (approximately), the reaction mixture was diluted with 300 cm of water and extracted twice with 100 cm of ethyl ether. The ether-containing phase is washed with water, dried over magnesium sulphate and evaporated under reduced pressure. Chromatographic residue on silica gel using cyclohexane-ethyl acetate (90:10 by volume). Thus, 1.8 g of o6-ztil-2-fennl-4-quinolinebutanoethyl, melting at 76 ° C, is obtained.
2-Phenyl-4-quinolinebutanoate is produced by esterification. The acid corresponding to that described in Example 23 is obtained with ethanol in the presence of sulfuric acid.
Example 25. Act as in example 23, using as starting materials 4 g of 2-phenyl-5-quinoline-pentanoic acid in 80 cm of chloroform, 1.05 cm of thionyl chloride and 6 cm of diethylamino
The residue obtained is chromatographed on silica gel using cyclohexane-ethyl acetate (50:50 by volume) as eluant. Thus, 2.7 g of N, N-diethyl -2-phenyl-4-quinoline-pentylnamide are isolated as a yellow oil. The NMR spectrum of the proton in deuterium-containing chloroform has a trace that is thicker than the characteristics: Ar – CH – CH, 8: 3.13 ppm;
, 8: 2.32 ppm;
H, 0: 7.68 ppm;
.-CHi-CH-CON: 1.84 ppra
2-Phenyl-5-quinolinepentanoic acid can be obtained as follows.
I. Preparation of -oxo-2-phenyl-4-quinoline-pentanoic acid.
To a suspension of sodium ethylate (prepared from 0.92 g of sodium and 2.34 cm of ethanol) in 200 toluene, a solution of G-oxo-2-phenyl-4-quinoline propionate-50 ml of toluene is added at 100 ° C for 5 minutes. The heating was heated for one hour at 100 ° C, after which 4.4 cm of ethyl acrylate was added; heating was carried out for 3 hours 30 minutes, after which 2.2 cm of ethyl acetate was added and the reaction mixture was stirred overnight. Bring the mixture to ambient temperature (about 20 seconds), add 35 cm of acetic acid to it.
15
20
25
4.6 g o-co-2-phenyl-4-x-olynolane of new acid, 2.15 g of 98% hydrazine hydrate, 2.4 g of potassium hydroxide in the form of solid particles, and 14 cm of diethyl lenglycol. In this way, 4 g of 2-phenyl-4-quinoline-pentanoic acid is obtained, whose NMR spectrum by proton in deuterium-containing chloroform is as follows: Ar - CH, o: 3.16 ppm
- Shg-COOH, fi: 2.37 ppm
Ar —CH —CH —CH —CH —COOH: 1.83 ppm 7.59 ppm
Example 26. To a suspension of 2.5 g of 2-finsht-4-quinolinpropanoic acid in 100 cm of poroform was added 3.78 cm of triethylamine, and after cooling, 1.24 g of ethyl chloroformate were added to the mixture under nitrogen. The mixture is permeated for 40 minutes at ambient temperature (approximately 20 ° C) after which it is introduced in small amounts by 1.05 g of N-methyl-2-butanamine chlorohydrate. The mixture is stirred for 20 hours at ambient temperature (about 20 ° C). After evaporation, it is dissolved, then 150 cm of water and 50 cm of body are under reduced pressure of half ethyl ether. The residue is dissolved in ethyl acetate. The organic phase is decanted. - Tate, wash the organic phase with water, dry over sulfate, magnesium and evaporate under reduced pressure. The resulting residue is chromatographed on silica gel using a mixture of
 - j; Lj. And ij rjjiri i v: .riyT. ii.i-i 1I LTiK1-LCHS; PGI M
cyclohexane-ethyl acetate (90:10 by volume is subjected to chromatography
him) as eluant. Thus, the pressure on the silica gel
saturated aqueous sodium carbonate solution, dried on magnesium sulfate. The residue obtained after evaporation of the solvent at a lower temperature.
This gives 6.6 g of A-ketoester, which is dissolved in 130 cm.
the first time chromatographic using a mixture of cyclohkksan-toluene-distilamine (80: 15: 5 by volume).
6 n. hydrochloric acid solution, and then heated. . ".
with reflux during the night. Cool the second 40 times using a mixture of the solution before, alkalinize to cyclohexane-toluene-diethylamine (90: pH 9 with 60 cm concentrated: 7.5: 2.5 by volume) and a third time with a mixture of hexane-ethyl acetate (50 : 50 by volume). The resulting residue is dissolved in acetone and after the hydrochloric acid is added in ethyl ether, the substance is obtained as crude hydrochloride. This product is recrystallized in isopropanol-50 isopropyl ether. After
ammonium hydroxide and then acidified to pH 4 with glacial acetic acid.
The aqueous phase is extracted three times with 150 cm of ethyl ether, and the organic phase is dried over magnesium sulfate and evaporated under reduced pressure. So get
4.7 g of 6-oxo-2-phenyl-4-quinolinpentaic acid, melting at 13b C. II. Preparation of 2-phenyl-4-quinolin-pentanoic acid.
Act as in the preparation of the 2-phenyl-4-quinolinbutanoic acid described in Example 23, however, as starting materials,
 restore the basicity of the product using 2 n. sodium hydroxide, extraction in ethyl acetate and evaporation at a pony pressure of 55 give 0.45 g of N-methyl-1-M-methyL-propyl-2-phenyl-4-quinoline propanamide as an oil, the NMR spectrum of which is in proton in deuterium-containing chloroform has the following characteristics:
0
five
0
five
4.6 g o-co-2-phenyl-4-x-olynol-ethanolic acid, 2.15 g of 98% hydrazine hydrate, 2.4 g of potassium hydroxide in the form of solid particles and 14 cm of diethylene glycol. Thus, 4 g of 2-phenyl-4-quinoline-pentanoic acid is obtained, the NMR spectrum of which, according to the proton in deuterium-containing chloroform, has the following characteristics: Ar – C 6, o: 3.16 ppm;
- Shg-COOH, fi: 2.37 ppm;
Ar — CH — CH — CH — CH — COOH: 1.83 ppm; 7.59 ppm.
Example 26. To a suspension of 2.5 g of 2-finsht-4-quinolinpropanoic acid in 100 cm of poroform was added 3.78 cm of triethylamine, and after cooling, 1.24 g of ethyl chloroformate were added to the mixture under nitrogen. The mixture is permeated for 40 minutes at ambient temperature (approximately 20 ° C) after which it is introduced in small amounts by 1.05 g of N-methyl-2-butanamine chlorohydrate. The mixture is stirred for 20 hours at ambient temperature (about 20 ° C). After evaporation of the solvent under reduced pressure, the resulting residue is dissolved in ethyl acetate, the organic phase is washed
 - j; Lj. And ij rjjiri i v: .riyT. ii.i-i 1I LTiK1-LCHS; PGI M
pressure chromatography
saturated aqueous sodium carbonate solution, dried on magnesium sulfate. The residue obtained after evaporation of the solvent at a lower temperature.
Pressure on silica gel, and
the first time chromatographic using a mixture of cyclohkksan-toluene-distilamine (80: 15: 5 by volume).
. . ".
the second time using a mixture of cyclohexane-toluene-diethylamine (90:: 7.5: 2.5 by volume) and the third time reducing the basicity of the product with 2N. sodium hydroxide, extraction in ethyl acetate and evaporation at a pony pressure of 55 give 0.45 g of N-methyl-1-M-methyL-propyl-2-phenyl-4-quinoline propanamide as an oil, the NMR spectrum of which is in proton in deuterium-containing chloroform has the following characteristics:
Alt
-cm rco-N,
N-
i
3d
Qhj
27
8: 3.52 ppm;
S: 2.78 ppm;
S: 2, -65-2., 78 ppm;
(: 7.73 ppm.
Example 27, B for
min heated with reflux 2.93 g
methylene chloride. Osu2-- / 2-fesh-4-quinolyl / -oxy-propionic acid and 2.2 cm of thionyl chloride in 75 cm of chloroform. The solvents are removed under reduced pressure, and the resulting residue is added over 15 minutes to a pre-cooled to a solution (10.3 cm) di-phylacate in 100 cm BI for 1 hour and 30 minutes under pi (stirring is added, followed by o) The phase is heated six times with MiiiBawT 100 cm of water, discharged on magnesium sulfate and evaporated under reduced H (|) m pressure. The residue obtained is ematographed on silica gel, using a mixture of cyclic hexane ethyl acetate (50:50 by volume) as eluant. I The resulting residue is recrystallized in isopropyl ether. Thus, 2.09 g of K, K-dihegyl-2/2-phenyl-4-quinolyl-oxy-n:)) opanamide, melted at, is recovered.
2-L / 2-Phenyl-4-quinolyl-oxy-1-pro-ponicic acid is obtained by ohm-a corresponding ethyl ester with a normal sodium hydroxide solution. The resulting re has a melting point
. .
2- [2-Phenyl-4-quinolyl] -oxy 1-pro-pyrnatethyl is prepared as follows: ohm
To a stirred suspension of 6.63 g of 2-phenyl-4-quinolinol and 8.3 g of potassium carbonate in 200 cm of methyl ethyl ketone are added dropwise 4.3 cm of 2-bromo-ropionate-ethyl. The mixture is heated for 3 hours under reflux. The mixture is brought to ambient temperature over jDjbi (approximately 20 ° C), the insoluble matter is wrung out, the solvents are removed under reduced pressure. The residue is dissolved in 100 cm of petroleum ether (40-70 ° C) and drained. taKHM 9.2 g of Lenil-4-quinolyl / -oxy-propionate ethyl, melted at 80 ° C, is obtained.
Example 28; For 3 hours, 1.1 g of 4-G2 / - phenyl-4-quinolyl-oxy-j-butanoic acid is heated under reflux. lots and. 0.53 cm of thionyl chloride in
161475928
20 cm of chloroform. Solvents are removed under reduced pressure. Then, 20 cm of chloroform is added to the residue and 2.2 cm of diethylamine are added dropwise while stirring. Stirring is carried out for 2 hours at ambient temperature (about 20. ° C), then the solvent is evaporated. under reduced pressure; and the residue is dissolved in 50 cm of water and 50 cm of ethyl acetate. The aqueous phase is extracted three times with 20 cm of ethyl acetate. The organic phases are collected, washed with 50 cm3 of water, dried over magnesium sulfate and evaporated under reduced pressure. The residue obtained is chromatographed on silica gel using a mixture of cyclohexane-ethyl-2Q acetate (50:50 by volume) as eluant. The residue obtained is dissolved in acetone and after the addition of a solution of hydrochloric acid taken in ethyl ether, 0.47 g of hydrochloride N, K-cyr 25 ethyl 4- / 2-phenyl-4-quinolyl-3-hydroxy-3- is obtained. butanamide, p.pav right at .140 ° С.
C / 2-Phenyl-4-quinolyl-oxy 3-butanoic acid is prepared as follows.
.1, Preparation of 4- / 2-phenyl-4-quino30
lil / -ox-butanol.
35
40
45
50
55
With stirring, 0.713 g of sodium in the form of fine particles is added to 30 cm of methanol. Stirring is carried out for 10 minutes at ambient temperature (about 20 ° C), after which 24.8 cm of 1,4-butanediol are introduced. Heating is carried out to remove methanol by distillation to 160 ° C and maintain this temperature for 15 minutes. The mixture is cooled to 100 ° C and 30 mg of copper in powder form are added under a nitrogen atmosphere. The reagents are then mixed and 7 g of 4-bromo-2-phenylquinoline are added in small portions to them in 30 min. Then: m heating is carried out for 2 hours at 160 s. After cooling to ambient temperature (approximately), the reaction medium is dissolved in water, then the copper is removed by filtration, and the filtrate is extracted in chloroform. The organic phase is washed with water, dried over magnesium sulphate and evaporated under reduced pressure. After two recrystallisations in a mixture of cyclohexane-ethyl acetate (70:30 by volume), 2.83 g / 2-phenyl-4-quinolyl -4 is obtained.
.1, Receiving
thirty
lil / -ox-butanol.
five
0
five
0
five
With stirring, 0.713 g of sodium in the form of fine particles is added to 30 cm of methanol. Stirring is carried out for 10 minutes at ambient temperature (about 20 ° C), after which 24.8 cm of 1,4-butanediol are introduced. Heating is carried out to remove methanol by distillation to 160 ° C and maintain this temperature for 15 minutes. The mixture is cooled to 100 ° C and 30 mg of copper in powder form are added under a nitrogen atmosphere. The reagents are then mixed and 7 g of 4-bromo-2-phenylquinoline are added in small portions to them in 30 min. Then: m heating is carried out for 2 hours at 160 s. After cooling to ambient temperature (approximately), the reaction medium is dissolved in water, then the copper is removed by filtration, and the filtrate is extracted in chloroform. The organic phase is washed with water, dried over magnesium sulphate and evaporated under reduced pressure. After two recrystallisations in a mixture of cyclohexane-ethyl acetate (70:30 by volume), 2.83 g / 2-phenyl-4-quinolyl -4 is obtained.
ten
15
25
oKCH-j6yTaHoj a, melted at.
Ii. Preparation of -4-U2-phenyl-4-quinolyl / -oxy-butane;
To cooled to solution. 2.25 g of chromic anhydride in 5 cm of 90% acetic acid is slowly added a solution of 2.20 g / 2-phenyl-4-quinolyl-4-hydroxy 3-butanol in 10 cm of glacial acetic acid. The temperature of the mixture is increased with ipne up to 20 ° C, after which the reagents are stirred for one hour at this temperature. 50 cm of ethanol is added, after which the solvents are evaporated under reduced pressure, and the resulting residue is dissolved in 100 cm of water, and the solution is dried out, insoluble. my substance and wash it several times in water. 15 cm of a normal solution of sodium hydroxide is added to the insoluble matter and the reagents are heated-during the reaction for 2 hours. The insoluble material is removed by filtration and the filtrate is acidified using glacial acetic acid. The precipitate is drained. 0.740 g of 4- (2-phenyl-4-quinolyl) -oxyT-butanoic acid is obtained, melting
at 264 ° 9.
Example 29. Operate as in Example 28, using as starting materials 1.25 g of 3- (2-phenyl-4-chi.nolyl) -oxyl-propanoic acid, 5 1.25 cm of thionyl chloride per 100 cm of chloroform and 2.66 cm diethylamine. After chromatography of the residue, carried out on silica gel using cyclo LodO hexane-ethyl acetate (50:50 by volume) as eluant, 0.43 g of H, K-diethyl-3- / 2-phenyl- 4-quinolyl / -oxy-propanamide, melted at 94 ° C.
3- [2-Phenyl-4-quinolyl] -oxy-pro-45 panoic acid having a melting point of 172 ° C can be obtained by oxidation of (2-phenyl-4-quinolyl) -oxy-propanol, obtained by 4-bromo-2-phenylquinoline with 1,3-propane diol sodium monosol by the methods described in Example 28 for the preparation of (2-phenyl-4-quinolsh1) -4-hydroxy 3-butanoic acid
thirty
diethylamine in 20 cm ba hydrofuran
After chromatography using as a mixture cyclohexane-ethyl volume) and recrystallization with isopropyl ether
H, -diethyl-2- | / 3-phenyloxy-propanamide, melt 117 ° C.
2- 1 - / 3-Phenylisoquin propanoic acid in a semi.
A mixture of 2., 42 g of 3-phenol linole, 8 cm of b-brompr and 5.4 g of sodium carbonate of 2-butanone is kept at a bale for 96 hours
The solvent is evaporated under reduced pressure. Add water and extract water with 50 cm of chloroform. About phase noschat on sulfate soar solvent p pressure. Chromium residue on silica gel using eluant, cyclohex mixture (1: 1 by volume). The first evaporations give 1 g of a brew and treated with a liquor (sodium hydroxide ethanol at ambient temperature (about)) under reduced pressure of 50 cm of water, washed with 5 ethyl ether aqueous concentrated solution and extracted three times with 5 form of magnesium sulfate, filter | and evaporated to dryness under pressure. 0.78 1-isoquinolyl / -oxy -product is obtained.
Example 31. With / 2-phenyl-4-quinol / -ti acid in 24 cm chlorof 0.65 cm thionyl chloride, stirred during the treatment of ambient 20 ° C). The reaction mixture is up to 5 ° C, after which, when nium is added, 2.5
Example 30. Act on amine. Stir yet
measure 6, using 0.78 g / 3-phenyliso- as starting materials. nolyl / -oxy3-propanes 6th acid, 0.52 g of carbonyldiimidazole and 0.82 cm
hour at a temperature of about 20 ° C (about 20 ° C), vapors when 50 cm are introduced into the residue
0
five
five
0
5 o
5 o
0
diethylamine in 20 cm anhydrous tetrahydrofuran
After chromatography on silica gel using a mixture of cyclohexane-ethyl acetate (1: 1 by volume) and recrystallization in isopropyl ether as eluant, 0.53 g is obtained.
H, -diethyl-2- | (3-phenyl-1-isoquinolyl) - hydroxy-propanamide, melted at 117 ° C.
2- 1 - / 3-Phenylisoquinolyl-oxy-propanoic acid was prepared as follows.
A mixture of 2., 42 g of 3-phenyl-1-isoquino-linol, 8 cm of b-bromopropionate of ethyl and 5.4 g of sodium carbonate in 20 cm of 2-butanone is kept at boiling for 96 hours.
The solvent is evaporated under reduced pressure. 50 cm of water are added and the aqueous phase is extracted three times with 50 cm of chloroform. The organic phase is present on magnesium sulfate and the solvent is evaporated under reduced pressure. The residue is chromatographed on silica gel, using cyclohexane-ethyl acetate (1: 1 by volume) as eluant. The first fractions after evaporation give 1 g of the substance, which is treated for 2 hours with 2 cm of liquor (sodium hydroxide) and 20 cm of ethanol at ambient temperature (about). The ethanol is removed under reduced pressure, 50 cm of water are added, the aqueous phase which is poured into 50 cm of ethyl ether is acidified with concentrated hydrochloric acid and extracted three times with 50 cm of chloroform. The organic phase is dried over magnesium sulphate, it is filtered and evaporated to dryness under reduced pressure. 0.78 g of 2- (3-phenyl-1-isoquinolyl) -oxy-propanoic acid is obtained.
Example 31. To a suspension of 2.5 g of (2-phenyl-4-quinol) / -ty o3-ac acid hydrochloric acid in 24 cm of chloroform, 0.65 cm of thionyl chloride was added, followed by stirring for 2 hours at ambient temperature (approximately 20 ° C). The reaction mixture is cooled to 5 ° C, after which 2.5 cm of diethyl are added with stirring.
hour at ambient temperature (about 20 ° C), the solvents are evaporated under reduced pressure, and 50 cm of water and 50 cm are introduced into the residue.
ethyl acetate; The organic phase is decanted, the aqueous phase is extracted with 50 cm of ethyl acetate. The organic phases are collected, washed twice with 20 cm of water, then 20 cm of a normal solution of ammonium hydroxide and, twice, 10 cm. of water, dried after magnesium sulfate and : tipped at reduced pressure. The radiated residue of chromium-athographic acid on silica gel using cyclohexane-ethyl acetate (50: 5 (Vno volume)) as an e-gpoant is dissolved in acetone and after adding a solution of hydrochloric acid in ethyl ether and Recrystallization of the crude chlorohydrate in ethanol gives 0.68 g of chlorohydra-Tfi K, H-diethyl- (2-phenyl-4-quinolyl) - ti-oJ-acetamide, melted at.
; / 2-Phenyl-4-quinolyl / -thio-acetic acid was prepared as follows.
; 3 g of 4-chloro-2-phenylquinoline and 1.38 g of thioglycolic acid in 40 cm of pyridine are heated under reflux for 4 | h. After evaporation of the pyridium, 125 cm of water and 40 cm of water are introduced into the sediment under reduced pressure.
PI
sodium hydroxide solution 1N. The aqueous phase is washed twice with 50 cm of ethyl ether, spun up to pH 5 with glacial acetic acid and extracted three times with 50 cm of ethyl ether, the ester-phase is washed with water, dried on magnesium sulphate and evaporated at HilraceHHQM pressured. Thus, 3.2 g of (2-phenyl-4-quinolyl) -TiioJ-acetic acid, melting P1 & And 138 ° Co,
Example 32. To a suspension of 4.8 g of 2- [2-phenyl-4-quinolyl] -thio1-propionic acid in 48 cm of chloroform was added 1.24 cm of thionyl chloride. Stir for 15 minutes at ambient temperature (about 20 ° C), after which they are heated for 2 hours 30 minutes under reflux. The temperature of the mixture was adjusted to 50 ° C, after which 4.9 cm of diethyl amine was introduced over 20 minutes. Stir for another 39 minutes at 5 ° C, then another 30 minutes at ambient temperature (about 20 ° C) 4 The solvents are evaporated under reduced pressure. And 50 cm of water and 80 cm of ethyl ether are added to the residue. . The organic phase is decanted, and the aqueous phase is decanted.
extract twice 50 cm of simple ethyl sira. The organic phases are collected, washed twice with 20 cm.
5 water, once 20 cm 0.1 n. sodium hydroxide solution and 2 times 10 cm of water, then dried on. sodium sulfate and evaporated under reduced pressure. The residue obtained is dissolved in ethanol and, after addition of hydrochloric acid in ethyl ether and two recrystallisations in ethanol, 1.95 g of N, M-diethyl-2- (2-phenyl-4-hinot5-lilo) hydrochloride are added. -TioJ-propanamide, melted at 155 ° C.
2- [2-Phenyl-4-quinolyl] -thio-propionic acid can be prepared. -A similarly 2- [2-phenyl-4-quinolyl] -thio
0 acetic acid, the preparation of which is described in Example 31, using as starting materials 4.8 g of 4-chloro-2-phenylquinoline, 2.54 g of thiolactic acid and 50 cm of pyridium on a sieve. So get
5.3 g of 2- (2-fensh-1-4-quinolyl) -thio1-propionic acid, the NMR spectrum of which, using the proton in deuterium-containing chloroform, has the following characteristics:
0
five
0
8-CH / CH3 /, - COOH, 4.70 ppm;
S-CH / CH3 / -COOH, S: 1.65 ppm
Bc, 8:
He o (;
8.14 ppm; 8.22 ppm.
5.8
P p and M ep 33. Operate in Example 31, using 3.4 g of 3- 72-phenyl-4-quinolyl-thioJ-propionic acid, 0.88 cm of thionyl chloride and 3.5 cm as starting materials. diethylamine.
The residue obtained is dissolved in ethanol and. after addition of a solution of hydrochloric acid in ethyl ether and recrystallization in ethanol 5, 2.3 g of hydrochloride, diethyl 3- / 2-phenyl-4-quinolyl-thia} propanamide, are obtained, melting at 145 ° C,
3- / 2-Fench1-4-quinolyl / -thio1-propionic acid is prepared in the following Q way.
4.8 g of 4-chloro-2-fensh1quinoline-and 2.45 g of 3-mercaptopropionic acid in 50 cm of pyridine are heated under reflux for 11 hours. After treatment similar to that described in
Example 31 for 2; - (2-phenyl-4-quinolyl) -ty (s-acetic acid, 3.4 g of 3- (2-phenyl-4-quinolyl) -thio-propionic acid, spectrum NMR which by
33
the proton in the deuteron-containing chlorophome has the following (its characteristics;
S-CH, -Cl2, -COOH,
n
5: 3., A2 ppm | O: 2.8 ° ppm; about: 7.62 ppm; B, b 0: 8 ppm,.
Example 34. During 3 hours, 2.5 g / 2-phenyl 4-quinolyl / -2-hydroxypropanoic acid and 1.85 cm of thionyl chloride in 50 cm of chloroform are heated under reflux and the solvent is removed under reduced pressure, and the resulting residue is converted into state of suspension in 40 cm of chloroform.
To the resulting suspension, 1.05 cm of diallylamine and 2.63 cm of triethylamine in 75 cm of chloroform are slowly added with stirring, keeping the temperature at a level. The reagents are stirred for 15 minutes at ambient temperature (about 20 seconds), the solvent is evaporated under reduced pressure and the residue is dissolved in 50 cm of ethyl acetate and 20 cm of water. The organic phase is decanted, washed twice with 10 cm of water, then with 10 cm of a normal saline solution. acid and finally 10 cm of water.
After evaporation of the solvent under reduced pressure, the residue is dissolved in acetonitrile and crystallized by the slow addition of isopropyl ether. After recrystallization of the obtained residue in isopropyl ether in the presence of activated carbon black, 1.9 g of OH, K-dipropen-2-yl-2- / 2-phenyl-4-xynolyl / oxy-j-propanamide are obtained; Topl. 110 ° C.
P p i. meper 35., Operate as in example 19, using as starting materials 1,8 rod-methyl-2-phenyl-4-quinoline-propanoic acid in 20 cm of chloroform, 0.58 cm of thionyl chloride, 0.81 cm of N- methylcyclohexylamine and 1.88 cm of triethylamine in 20 cm of chloroform

The residue obtained is recrystallized in ethyl acetate. In this way, N-cyclohexyl N-methyl-phenyl-4-quinoline propanamide is obtained, melting at.
Example 36. Act as in Example 19, using as the starting material 1.8 g of SU, α-methyl-2-phenyl-j 4-quinolinepropanoic acid in 20 cm of chloroform, 0.58 cm of thionyl chloride.

61475934
1.44 cm of dihexylamine and 1.88 cm of trinethylamine in 20 cm of chloroform.
The residue obtained is chromography — pyioT on shtagel, using a mixture of cyclohexane-ethyl acetate (80:20 by volume) as eluant. The residue is dissolved in acetone and after addition of hydrochloric acid solution in ethyl ether and recrystallization of the crude hydrochloride obtained in ethanol-ethyl ether (I; 3 in terms of weight), 0.36 g of M.K. schorhydrate are obtained. α-dihexyl "1-me t1n-2-phenyl-4-quinolinpropanamide, melted at.
Example 37. Act as described in Example 19, using 1.1 g of ob-methyl-3-phenyl-20 1 yphthaline propanoic acid, 0.37 cm of thionyl chloride in 20 cm of chloroform and 2 cm of diethylamine in 20 cm of chloroform as starting materials.
The residue is chromatographed on a sapic-gel using cyclohexane-ethyl acetate (70:30 by volume) as elnran. 1 g of M, K-diethyl o -methyl-3-phenyl-1-naphthalene propanamide, melted at 70 ° C, is obtained in this manner.
(x-Ketil-3-a) Yenyl-1-naphthalenepropanoic acid can be obtained by the following formula
1o Preparation of en1b-1-naphthalene-methanol.
25
thirty
35
1.9 g of sodium borohydrate, is added to a stirred solution of 5.6 g of 3-fennl-1-naphthalenecarboxylateethyl in 80 cm of tertbutanol. Reagents 40 are maintained at reflux, then 16 cm of methanol is poured in for 2 hours and 10 minutes. Heating is continued at reflux for another 2 hours, then the reaction mass is cooled to 45 ambient temperature (approximately 20 ° C), 40 cm of water is added, then 4 cm of acetic acid and evaporation is carried out under reduced pressure. The residue is dissolved in 100 cm of chloroform and 100 cm of water. Organic phase. decanted, washed with tOO cm of water and evaporated under reduced pressure. The residue is chromatographed on silica gel using chloroform as eluant. Collect fractions containing 3-phenyl 1-naphthalene methanol. After evaporation carried out under reduced pressure, a residue is obtained, which is dissolved in methylene chloride,
50
35
washed with ammonium hydroxide solution. The organic phase is dried over magnesium sulphate and evaporated under reduced pressure.
 3.6 g of 3-phenyl-1-naphthalene-methanol is obtained, whose NMR spectrum by proton in deuterium-containing chloroform has the following characteristics: A - CH., OH,: 5.20 ppm;
Mothballs; H2otones,
H
Schyutony fenilovogo dra Noo,
iНмм р,
H
: S:
7.48 ppm; 7.67 ppm;
.)
: 7.71
ppt;
- J f about: 7.45 ppm. I 3. Phenyl-1-naphthalenecarboxylate ethnically prepared by esterifying 3- | -phenyl-1-naphthalenecarboxylic acid with ethanol in the presence of sulfuric acid.
: II, Preparation of 1-chloromethyl-3-phenyl-n phthaline.
I To a stirred solution of 1 g of 34feiil-1-naphthalenmethanol in 20 cm chl | 1 oroform, previously cooled with H (|) rb to 0 ° C, add 0.78 cm of thionyl chloride over 1 (|) min, after 4 (fero the reagent is left to rise to ambient temperature (about 20 ° C). At this temperature, the P Р: agents are stirred for 15 h, then the pg1 solvent is evaporated under reduced HciiM pressure. 1.1 g is obtained. -3-phenylnaphthalene, whose NMR spectrum by proton in deuterium-containing chloroform has the following characteristics:
S
Ar-CH Cl, Ng1 phthaline protons IT-, o
 - l
IV, 8
Feshilovye
protons Nmm p, 0;
5.08 ppm;
7,65 ррт
7,78ррт
7,44 ррт
1514759 -36
tetrahydrofuran reflux. The ambient temperature is restored (approximately) and g is added dropwise to 2 cm of glacial acetic acid. The tetrahydrofuran is evaporated under reduced pressure, and the resulting residue is dissolved in 100 cm of water and extracted twice with 50 cm of ethyl ether 10. The ether phase is washed with water, dried over magnesium sulphate and evaporated under reduced pressure. The residue obtained is dissolved in 25 cm3 of concentrated hydrochloric acid thief and 25 cm of glacial acetic acid.
The reaction mixture is heated for 4 hours under reflux, after which the acids are evaporated to a maximum at
2Q under reduced pressure, the residue is dissolved in 100 cm of water, the resulting solution is alkalinized to pH10 with a concentrated solution of ammonium hydroxide, and then extracted twice
25 50 cm. Simple ethyl ether.
The aqueous phase is acidified to pH 6 with acetic acid and extracted twice with 50 cm of ethyl acetate. The organic phase is dried over magnesium sulfate and
2Q is evaporated under reduced pressure. The residue obtained is chromatographed on silica gel using chloroform-acetic acid (9: 1 by volume) as the endpoint. 1 g of o6-methyl-3-fench1-1-naphthalenepropanoic acid was isolated, the NMR spectrum of which by the proton in deuterium-containing chloroform has the following characteristics:
Aromatic protons, 7.3-8.2 ppm
40
Ar-CH, Ar-CH ,, - gi-, Ar-CH / CH3 / -,
, -, and: 2.7-3.5 ppm about: 1.2 ppm.
.III c Obtaining o.-methyl-3-phenyl-1 naphthalenepropanoic acid.
O is slowly added to 15 cm of dry tetrahydrofuran under nitrogen atmosphere. 62 g of sodium hydride are added as a 60% dispersion in oil. Then a drop of V19od t solution of 2.69 g of methylmaldonate-dol in 15 cm of tetrahydrofuran, and then within 50 minutes a solution of 1.95 g of 1-chloromethyl-3-phenylnaphthalene in 30 cm of tetrahydrofuran. The mixtures are kept for an hour at an ambient temperature (approximately 20 sec.) P. IType. and then for 3 hours at
45
L and rm 38. Operate as in example 19, using as the initial product 1.2 g (1) enyl-4-quinolyl / -oxy-propanoic acid in 40 cm3 of chloroform, 0.89 cm1 thionyl chloride, 0 , 41 g of thiomorpholine and 1.15 skz of triethylamine in 20 cm of chloro-50 form.
The residue is subjected to chromatography on silica gel, using methylene-chlorine-55 REED as a zlüant, then a mixture of methylene chloride-ethyl acetate (95: 5 by volume) “This is obtained
O, 7 g of 4 2- / 2-phenyl-4-quinodyl / -oxy-propionyl-thiomorpholine, melted at 198 C.
Aromatic protons, 7.3-8.2 ppm
Ar-CH, Ar-CH ,, - gi-, Ar-CH / CH3 / -,
, -, and: 2.7-3.5 ppm about: 1.2 ppm.
Example 39. To a solution of 2 g of oL -me.T11l-2-fennl-4-quinazoline propanoic crescent acid in 20 cm of tetraglrofuran, 1.65 g of carbonyldiimidaeol is added to a lemmeculated solution. Stirring is continued for 20 minutes until gas evolution stops, after which another 1 hour, then 1.05 cm of diethyl amine is added. Stir for 5 days at ambient temperature (about 20 ° C), after which they are heated for 2 hours under reflux. The solvent was evaporated under reduced pressure and the resulting OS- (5; the residue was dissolved in 100 cm of ethyl ether. The organic phase was washed 2 times with 10 cm of water, then 2 times with 5 cm of a normal hydrochloric acid solution, and then 2 times with 5 see jn of a normal solution of sodium hydroxide and finally 2 times 5 cm of water. The organic phase is dried on magnesium sulphate and evaporated under reduced pressure. The residue is recrystallized twice in isopropyl ether. Tact; get 1.1 g of N, N - di-ethyl () 1, megkp-2 -fe 1 ylhiiazolin 4-pro | it, melted ppi UZ., at 0.5% in EtOH at 23 ° Co j3 -17.9 ± 2 ° -, 3
Ob-Methyl-2-phenyl-4-quinazoline propanoic acid can be obtained by separating d-methyl-2-phenyl-4-quinazoline propanoic racemic acid, in the following 35
I. Preparation of K- (1-phenyl-2-ox1; ethyl). o6 methyl-2-phenyl-47-quinazolinpropane-dias diastereomers.
  40
Under a nitrogen atmosphere, to a stirred solution of 59.1 g of o6-methyl-2-phenyl-4-quinazoline propanoic acid in 1800 cm of methylene chloride, 44.5 g of 2,2-dipyridyl disulfide and 45 of 27 g / - / o-phenylglycinol are added. The mixture of reagents is cooled to 0 ° C, after which 53 g of triphenylphosphine are introduced with a spatula over 15 minutes. The reagents are stirred for 21 hours at ambient temperature (about ZO C), after which the solvent is removed under reduced pressure, and the residue is dissolved in 1800 cm of ethyl acetate. The organic phase is successively washed with 450 cm, then 200 cm and then 100 cm of a normal solution of sodium hydroxide, then 2 times with 100 cm of water and, finally.
50
55
, n - (5 - jn 25 3
35
.
40
45
50
five
200 cm of a 10% sodium hydrosulfite solution, 100 cm of water and 100 cm of a saturated solution of sodium chloride. The organic phase is finally dried on magnesium sulfate and evaporated under reduced pressure. The residue is chromatographed under pressure from a gel-gel using chloroform-topuol-diethylamine (50: 44: 6, as per volume, him,) as the zlüant. I
 After recrystallization of two amide diastereomers, in acetonitrile, 18.1 g of N- / 1-phenyl-2-hydroxyethyl / oi-methyl-2-phenyl-4-xinase Slinppanamide-form L are obtained, washed out first, and then 15.4 g of N- / 1-phenyl-2-ox c ethyl / o, methyl-2-phenyl-4-quinazoline propanamide form B, which is washed second and which has a melting point equal to. Ii. Preparation of cv -methyl-2-phenyl-4-quinazoline propanoic acid by the correctant.
19 g of N- / 1-phenyl-2-hydroxyethyl / o, -M (: Chtil-2-phenyl-4-chiazoline-propane-amide-form A in 90 cm ice acetic acid and 90 cm of a concentrated solution of hydrochloric acid.
The acids are evaporated under reduced pressure, the residue is dissolved in 600 cm of water, alkalized to RP 10 with a concentrated ammonium hydroxide solution and washed with 100 cm of simple ethyl ethyl acetate. The aqueous phase is acidified to pH 5 with crystallized acetic acid. The precipitate is filtered off, washed with water and dried. Thus, 13.5 g of oi-methyl-2-phenyl-4-quinazoline propane hydrochloride are obtained. acids melting at 179.1 ° C; at 0.5% in glacial acetic acid at djy 4 + 2 °.
Example 40. The validity of Example 39, using 2 g of od-methyl-2-phenyl-4-quinazoline-propane left-handed rotary acid in 20 cm of tetrahydrofuran, 1.65 g of carbonyldi-midazole and 1.05 cm of diethylamine as starting materials. After two recrytic digests carried out in simple ch.opropyl ether, 1.3 g of N, N-diethyl -) - methyl-2-fe} psh-4-quinylproline propanamide praiovraiiiop. melt at 93.8 ° C.
At 0.5% in Eton at 23 (: g) +17,
Ob-Methyl-2-phenyl-4-quinazolinpropa nfu left-rotating acid can be obtained by analogy with its right-rotating eiantiomer (described in example 39), but using raw materials of 16.4 g N- / 1-fenil-2-hydroxyethyl / v-methyl-2-fesch-4-quinazoline propanamide in the form.
AT
8 (1 her
obtained according to example 39, see glacial acetic acid and see concentrated solution
l noi acid.
: 11.4 g. -Metsh1 2-phenyl-4- | -quinazoline propanoic levogravic acid, melting at 179.3 s, is obtained.
At 0.5% in glacial acid, uf D is -44.2 ° at 21 ° C.
Example 41, To a stirred solution, 2g. ob-methyl-2-phenyl-4-x} 1-azoline propanoic pro-rotatory acid in 20 cm of tetrahydrofuran; dfbavl 1.65 g of carbonyldiimidazole; Stirring of the reagents is carried out in
. T (1 hour at ambient temperature (until the end of the gas release), then add 1.03 cm of N-methyl isopropylamine, is stirred for three days at ambient temperature (about 20 ° C), then heated at reflux for 6 hours and add 1.03 cm of N-methylisop (ropylamica), then heat
- another 12 hours at reflux. After-treatment is similar to that described in Example 39. After two recrystallisations carried out in acetonitrile, 19 g of N-isopropyl-N-methyl methyl l-2-phenylquinazoline-4-propanamide, left-rotating, melt at 23 171,
D
At 0.5% in EtOH at 23 ° С -12.1i2o. .
PRI me R. 42. Operate according to Miepy 41, using 2 g-methyl-2-phenyl-4-quinazoline propanoic levorotating acid in 20 cm of tetrahydrofuran, 1.65 g of carbonyl imidazole and 1.03 sc N-methyl isopropylamine as the starting material.
After two recrystallisations in acetonitrile, 1.1 g of N-isopropyl-K-methyl- () (-methyl-2-phenyl-quinazo-1 in-4-propanamide, programing, melting at 171.0 ° C, are obtained.
At 0.5% in EtOH at 23 ° C oij, + 16.3i2,.
five
five
0
0
five
0
five
Following the same procedure and proceeding from compounds of the formula III, the following compounds are obtained.
Example 43. N, N-diethyl-2- (3-trifluoromethylphenyl) -4-quinazoline-propanamide; t, pl. 115 C.
. Example 44, N, N -diethyl-2-thienyl-4-quinazoline propanamide; m.p. Yub So.
Example 45. H, K-diethyl-6-bromo-2-phenyl-4-quinazoline propanamide; m.p. .
Example 46 K, N-diethyl-6-methoxy-2-phenyl-4-quinazoline-propanamide; m.p. . Example 47. H, H-diethyl-8-methyl-2-phenyl-4-quinazoline-propanamide; m.p. 80 ° C. .
Example 48, B, H-diethyl- (4-phenyl-2-quinolyl) -oxy-acetamide; Topl, 100 ° C.
Example 49. N, N-diethl- [2-phenyl-4-quinazolinyl] -oxy-acetamide; m.p. 113 ° С
Example 50., N, N-diethyl- [4phenyl-2-quinazolinyl] -oxy-acetamide, T.Sh1-. 88 ° C.
Example 51 N, M-diethyl- (3-phenyl-1-isoquinolyl) -oxy-acetamide, m.p. 102 ° C.
Example 52. N, N-diethyl- / 1-phenyl-3-isoxynolyl / -oxyl-acetamide; T.njio
Example 53. Y, K-diethyl-2- | (2-phenyl-4-quinazolinyl / 3-hydroxy-propanamide); m.p. LWO S.
Example 54 K, N-diethyl-2- [2-phenyl-4-quinazolinyl] -oxy1-propanamide; levogyrate; m.p. 160 ° C. ....
Example 55. S, H-diethyl-g2- | / 2-phenyl-4-quinazolinyl / -oxy-pro-papamide; dextro-rotatory; m.p. 160 ° C
Example 56, N, N-diethyl- (4-phenyl-2-quinolyl) -thio | -acetamide, chlorohydrate,
Example 57. N, N-diethyp- [3-phenyl-1-naphthyl] -oxy1-acetamide, m.p. 82 C. Example 58, S, K-diethyl-2- / e of 1kl-on tsh1 / -oxy-propanamcd1 t. Pl. 109 ° C. .
PRI, meper 59. K, M-diethyl-2- 112-phenyl-8-trifluorome-1-4-quinolyl / - hydroxy-propanamide; t.pl „b S.
Example 60. N, N-nH3THn-anb (ha-methyl-.-Phenyl-4-quinolein-acetamide; m.p.
The compounds of formula (I), a mixture of their stereomers, a salt of these compounds, or a mixture in combination with any other pharmaceutically acceptable substance can be used in pharmaceutical compositions. A drug based on them can be administered orally, parenterally, rectally or topically.
The compounds of formula (I) and their copolymers have interesting pharmacological properties. With peripheral-type benzodiazepine acceptors, these compounds are suitable for use in anxiolytic, anticonvulsant, anti-anginal drugs and for the treatment of conditions caused by immunosuppression.
The affinity of compounds of formula (I) for peripheral-type benzodiazepine acceptors is determined on rat kidney membranes when used as H-PK 11195 ligands | K-methyl N- / 1-methylpropyl / -1- / 2-chlorofate / 3-isoquinolinecarboxamide and is from 0.001 to 1.5 tM,
Affinity is determined by the ability of the bonds to displace the RR 11195 about their place of communication and is expressed by the value of K, which is calculated using the formula
a-
42
Table continuation
1C
50
 H
D
where C
the concentration of iH PK 11195 used;
affinity constant N RK
11195; compound concentration
necessary for 50% inhibition of the formation of the HKK 11195 bond (see table).
43
1614759
The compounds prepared according to the invention have low toxicity. 200 mg / kg orally administered to mice (the LD value was calculated after 3 days of observation using the cumulative method).
Dp use for medical purposes can be used for formate compounds (I) as they are, whether in the form of salts with pharmaceutically strong strong acids, if these salts exist, j Thus, the proposed method allows to obtain compounds of formula (I), which have low toxicity and prominently anti-xyolytic and anticonvulsant properties

权利要求:
Claims (1)
[1]
The invention The method of obtaining the formula
- (CH,) tt- (CHVCO-NC
Z
de A and B are the same or different, nitrogen or group V and W are hydrogen, halogen,.
C4-C5-alkyl, C, coxy, trifluoromethyl; Z is in the ortho or para position with respect to B and is phenyl, tne-NIL, pyridyl or phenyl substituted with one or two substituents selected from the group CpC-alkyl, coxy trifluoromethyl, nitro;
The X- (CH) - (CHR) -CO-NR, R2 chain is located in the ortho or pa position with respect to B. - hydrogen, C-C3 alkyl; R TL is the same or different C, -C-alkyl, linear or branched, Ce-C, is cycloalkyl, phenyl, (alkenyl, provided that the double bond is not 44
0
is located at position 1.2 through. with respect to nitrogen, or K and R 2 may form together with the nitrogen atom to which they are attached a pyrrolidine, piperidine, morpholine or thiomorpholine cycle; X is CH-RJ; t is 0.1, p 0.1 or 2, or X is oxygen or sulfur, then m 1, n 0.1 or 2, except for the compounds, where A and B are each nitrogen and Z is in the position a pair with respect to B and X is a group CH-Rj. with A, the group is CH, B is nitrogen, Z is in the ortho position with respect to B, X is oxygen and R is hydrogen, and m + n is 0.2 or 3, 5 or their diastereomers, racemates
enantiomers or addition salts thereof, characterized in that the compound of the general formula /
five
0
thirty
X- (CH2), - CCH) -CO-E
one
where E is C —C alkoxy, C, —C alkoxycarbonyloxy}
N is an imidazolyl residue; X, a, b, v, w, z, r, t, n have
specified values
subjected to interaction with the amine of the General formula /
45
HN
R
where R and R 2 - have the indicated meanings, followed by isolation of the desired product, or separation of eantio, measures, or translation of the resulting product into an acid addition salt.

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公开号 | 公开日 | 专利标题

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SU1614759A3|1990-12-15|Method of producing amides, their diastereomers, racemates or their acid-additive salts

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KR850000891B1|1985-06-26|Process for preparing trisubstituted imidazole derivatives

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SU1251801A3|1986-08-15|Method of producing 2-substituted 4-amino-6,7-dimethoxyquinolines or pharmaceutically acceptable salts thereof

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IL32091A|1973-02-28|Derivatives of furan,pyrrole and thiophene

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SU633471A3|1978-11-15|Method of obtaining n-substituted trichloracetamidines or salts thereof

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SU719499A3|1980-02-29|Method of preparing 1,2,3,4,6,7-hexahydro-11 b alpha-h-benzo|-quinolysin derivatives or their salts

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PL126032B1|1983-07-30|Process for preparing novel derivatives of 5-phenyl-2-hydroxytetrahydrofuran

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SU481155A3|1975-08-15|Production method - | morphinans

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SU479290A3|1975-07-30|The method of obtaining 2- | -6,7 benzomorfan

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SU1440349A3|1988-11-23|Method of producing orthocondensed derivatives of pyrrole

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US4567177A|1986-01-28|Imidazoline derivatives as α2 -antagonists

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Anderson et al.1984|Synthesis and evaluation of furan, thiophene, and azole bis [| methyl] derivatives as potential antineoplastic agents

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SU1039442A3|1983-08-30|Process for preparing derivatives of phenylpiperazine

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US5457201A|1995-10-10|Chiral resolution process

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SU468423A3|1975-04-25|Method for preparing 6-aza-3n-1,4-benzodiazepines

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SU797580A3|1981-01-15|Method of preparing isoquinoline derivatives, their salts, racemates or optical isomers

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SU417946A3|1974-02-28|

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SU500747A3|1976-01-25|The method of obtaining derivatives of bornamine

同族专利:

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公开号 | 公开日

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SU1544186A3|1990-02-15|

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US4788204A|1988-11-29|

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AT47840T|1989-11-15|

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JPS625946A|1987-01-12|

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ES557168A0|1987-05-01|

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HU195641B|1988-06-28|

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ES8705227A1|1987-05-01|

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IL78969D0|1986-09-30|

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ZA863993B|1987-01-28|

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AU579473B2|1988-11-24|

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ES8705228A1|1987-05-01|

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CA1264160A|1990-01-02|

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IL78968D0|1986-09-30|

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ES8800660A1|1987-11-16|

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HUT42071A|1987-06-29|

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PT82673A|1986-06-01|

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HUT42072A|1987-06-29|

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ZA863992B|1987-01-28|

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ES8704732A1|1987-04-16|

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CA1251206A|1989-03-14|

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MA20696A1|1986-12-31|

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DE3662045D1|1989-03-16|

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DK252386D0|1986-05-29|

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PT82674B|1988-08-17|

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AU579472B2|1988-11-24|

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EP0205375B1|1989-11-08|

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ES8705225A1|1987-05-01|

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MA20697A1|1986-12-31|

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ES557166A0|1987-05-01|

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AT40689T|1989-02-15|

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TNSN86081A1|1990-01-01|

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NZ216331A|1989-04-26|

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EP0210084B1|1989-02-08|

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DE3666813D1|1989-12-14|

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EP0205375A1|1986-12-17|

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FR2582514A1|1986-12-05|

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NO862133L|1986-12-01|

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EP0210084A1|1987-01-28|

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SU1470182A3|1989-03-30|

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US4728647A|1988-03-01|

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GR861368B|1986-09-29|

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IL78968A|1989-07-31|

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ES8704731A1|1987-04-16|

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HU195642B|1988-06-28|

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AU5803086A|1986-12-04|

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ES555557A0|1987-04-16|

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NO862134L|1986-12-01|

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PT82674A|1986-06-01|

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TNSN86080A1|1990-01-01|

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IL78969A|1989-07-31|

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ES557167A0|1987-11-16|

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SU1508957A3|1989-09-15|

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DK252386A|1986-12-01|

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NZ216330A|1989-04-26|

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ES8705226A1|1987-05-01|

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DK252286D0|1986-05-29|

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ES557170A0|1987-05-01|

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PT82673B|1988-08-17|

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SU1537135A3|1990-01-15|

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SU1470183A3|1989-03-30|

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FR2582514B1|1988-02-19|

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AU5803186A|1986-12-04|

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ES557169A0|1987-05-01|

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ES555558A0|1987-04-16|

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GR861369B|1986-09-29|

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DK252286A|1986-12-01|

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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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FR858508111A|FR2582514B1|1985-05-30|1985-05-30|AMIDE DRUGS, NEW AMIDES AND THEIR PREPARATION|

---