Method of producing derivative substituted amide

专利摘要:
The invention relates to heterocyclic compounds, in particular the preparation of derivatives of substituted amides (A3) of the general formula RC (0) -NH-Het, where R is phenyl (it can be substituted by lower alkyl, 1,2 - by F atoms or OH, in 3- m or 4th position - alkyloxy, methylenedioxy or in 3 positions - dialkylamino), 3-pyridyl, 3-alkyloxypyridyl, thienyl, alkylthienyl, furyl, alkylpyridazinyl or tetrahydropyridyl; Het - 7-halo-2-quinolyl, 1,8-naphthyridin-2-yl (it may be substituted in the 7th position with halogen, alkyl, alkyloxy, alkyloxyalkyloxy, C — C-alkenyloxy-1 l, Cd — C-alkylkyloxy, , alkylthio -, - benzylthio, phen.oxy (it may be substituted by F, C1, Br in position 2, or methoxy, 1st or СНх, or pyridyloxy, or alkylpiperidyloxy), while, Het - 7- halo-2-quinolyl, then R. phenyl, and the said H- or isoalkyls or alkyl parts have 1-4 carbon atoms, which have anxiolytic, hypnotic, anticonvulsant, pro- tivoepileptic and muscle relaxant effects that can be used in medicine. The goal is to create new and more active substances of the indicated class. Synthesis of A3 is carried out by reacting the corresponding amine and acid in the presence of K, H-carbonyldiimidazole or its derivative in the presence of a nitrogen-containing base. with the preliminary introduction of the protection of the hydroxy group. Toxicity A3 LDjp 7 / 300-900 mg / kg. New A3 have antimicrobial action against microbes that have become resistant to traditional antibiotics. 2 tab. WITH | with
公开号:SU1417797A3
申请号:SU853923698
申请日:1985-07-18
公开日:1988-08-15
发明作者:Котрель Клод；Гийон Клод；Руссель Жерар；Торан Жерар
申请人:Рон-Пуленк Санте (Фирма)；
IPC主号:

专利说明:

 sn
The invention relates to a method for producing new substituted amide derivatives having pharmacological properties that can be used in medicine as pharmaceuticals. I
The purpose of the invention is new ones.
compounds with a higher biological activity than the structural analogue of the same effect.
Example 1. To a solution of 10.9 g of p-toluic acid in 100 m of anhydrous tetrahydrofuran was added 12.9 g of N, m-carbonyldiimidazole. Note Immediate outgassing. The mixture is stirred for 1 hour at, until gas evolution is complete. Then, 8.9 g of 2-amine-7-chloro-1,8-naphthyridine are added and heated at reflux for 20 hours. The mixture is then poured onto 1000 cm of distilled water, and the resulting residue is filtered off, washed with water and dried on the air.
The resulting compound (13.6 g, T.S.I. 222 ° C) is dissolved in A70 cm of boiling ethanol. After 4 hours of cooling at 4 ° C, the crystallized precipitate is separated by filtration, washed with 3 times 20 cm of ethanol and dried under reduced pressure (0.067 kPa). 10 g of N- (7-chloro-158-naphthyridin-2-yl) -4-methyl-benzamide are obtained, melting at 228 ° C.
Example 2 o Acting as indicated in Example 1, however, 5.2 g of cyclopropylcarbonic acid, 9.8 g of N, N-carbonyldiimidazole and 7.2 g of 2-amine-7-chloro-1.8-1 are used. naphthyridine. The compound obtained by precipitation in water (10 g, mp 250 ° C) is dissolved in 530 cm of boiling 2-propanol.
After 4 hours of cooling at If C, the crystallized solid was separated by filtration, washed 3 times with 20 cm of 2-propanol and dried under reduced pressure (0.067 kPa). "Obtain 7.5 g of N- (7-chloro-1 , 8 naphthyridine-2-Sh1) cyclopropanecarbokeamide, melting at 250 C.
Example 3. They act in the same way as in Example 1, however, 13.7 g of cyclopropanecarboxylic acid, or 25.8 g of N, N -carbonyldiimidazole and 17.5 g of 2-amine-7-methoxy-15 7-naf 1 iridine. The compound obtained by precipitation in water (24.3 g, mp. 100 ° C) is purified by chromatography on a column with a diameter of 40 mm,
containing 400 g of silica (0.040-0.063 mm), eluting with a mixture, (95-5 by volume) of methylene chloride and methanol, to obtain fractions in an amount of 100 cm. After concentrating dry 6–17 under reduced pressure (4 kPa) 17 g of solid are obtained, melting at 170 ° C. The compound is dissolved in 120 cm of boiling ethanol.
5 After cooling for 2 hours at A C, the crystallized solid is separated by filtration, washed twice with 10 cm of anole and dried under reduced pressure.
0 (0.067 kPa). 12.5 g of N- (7-methoxy-1,8-naphthyridin-2-yl) cyclopropanecarboxamide are obtained, melting at
.
2-Amin-7-methoxy-1,8-naphthyridine 5 can be obtained in accordance with known methods.
Example 4. They act in the same way as in Example 1; however, 4.8 g of cyclopropanecarboxylic acid are used as starting materials.
acids, 9.07 g of N, N -carbonshvdiimidazole and 10 g of 2-amine-7-phenoxy-1,8-naphthyridine. The compound obtained by precipitation in water (11.2 g, mp approx.) Is dissolved in 200 cm of boiling ethanol. After 2 hours of cooling at 4 ° C, the crystallized solid is separated by filtration, washed twice with 10 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa). 6.4 g of K - (- phenoxy-1,8-naphthyridine-2-Sh1) cyclopropanecarboxamide, melting at 190 ° C, are obtained.
2-Amino-7-phenoxy-1,8-naphthyridine can be prepared as follows.
A mixture of 27 g of 2-amine-7-chloro-1,8-naphthyridine, 141. g of phenol is heated for 20 hours at 120 ° C.
p and 19.8 g of potassium hydroxide tablets by 85%. The mixture was dissolved in 300 cm aq. 4 n. sodium hydroxide solution and extracted with 250 cm of methylene chloride.
e The aqueous phase is extracted another 2 times with 200 cm of methylene chloride. The organic extracts are washed twice 150 cm 4 n. sodium hydroxide, and then 250 cm of distilled water, dried
five
0
five
on magnesium sulfate n KOHueHTpHpiTOT dry at a reduced pressure (4 kPa).
The resulting compound (30.5 g, mp. 190-194 ° C) is dissolved in 400 cm of Boiling acetonitrile. After 2 hours of cooling at 4 ° C, the crystallized solid is separated by
95 ° C), dissolved in 15 cm of boiling methanol. After 3 hours of cooling at 20 ° C, the crystallized solid is separated by filtration, washed 3 times with 15 cm of methanol and dried at 40 ° C under reduced pressure (0.067 kPa). 13.2 g of N- (7-phenoxy-1,8-naphthyridin-2-yl) -1.4 are obtained.
Shchogos at 95 C.
Example 8. To a solution of 5.4 g of 2-amine-7-chloro-1,8-naphthyridine in 60 cm of pyridine was added slowly 4.2 g of 15 benzoyl chloride, keeping the temperature at about. After keeping the solution for 3 hours at a temperature of about 20 ° C, the compound is precipitated at 340 cm distilled20
filtration, wash another 20 cyclohexadiene-1-carboxamide, melt-acetonitrile, and dry at 45 ° C. under reduced pressure (0.067 kPa); 23.4 g of 2-amine-7-phenoxy-1,8-naphthyridine, melting at .
Example 5. They operate under conditions similar to those specified in Example 1, however, 5 g of cyclobutanecarboxylic acid, 10.5 g of N, N -carbonyldiimidazole and 7 g of 2-amine-7-chloro-1 are used as starting materials. , 8- naphthyridine. The compound obtained by filtration (9 g, mp) is dissolved in 150 cm of boiling acetonitrile. After 3 hours of cooling at 20 ° C, the crystallized substance is separated by filtration, washed with 3 times 25 cm of ethyl ether and dried at 35 ° C under reduced pressure (0.066 kPa).
6.3 g of N- (7-chlorop-1,8-naphthyridin-2-yl) -cyclobutyriconcarboxylate, melting at 192-194 ° C, are obtained.
Example 6. The conditions are similar to those indicated in Example 1, however, 6.2 g of 1,4-cyclohexadiene-1-carboxylic acid, 8 g of N, N - carboni diimidazole and 8 g of 2- are used as starting materials. amine-7-chloro-1,8-naphthyridine. Connection, Pog
The precipitate obtained by precipitation in water (1 mp. 205 ° C) is dissolved in 250 cm of boiling ethanol. After 2 hours of cooling at 4 ° C, the crystallized solid is separated by filtration, washed three times with 15 cm of ethanol, and dried at 40 ° C under reduced pressure (0.067 kPa). 4.2 g of S- are obtained (7-chloro-1 , 8-naphthyridine-2-yl) -1,4-diclohexadien-1-carboxamide, melting at 210 C.
Example 7. They operate under conditions similar to those specified in Example 1, however, 12.4 g of 1,4-cyclohexadiene-1-carboxylic acid and 16.2 g of N, N -carbonyldiimidazole and 21.4 are used as starting materials. g 2-amine-7-phenoxy-1,8-naphthyridine. The compound obtained by precipitation, carried out in water (17.2 g, so pl.
bathroom water. After drying in air, the solid obtained is dissolved in 88 cm of boiling ethanol. After 3 hours of cooling with the crystallized solid, it was separated by filtration, washed with 2 times 5 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa), thus obtaining 4.95 g of N- (7-hlop-1 , 8-naphthyridine-2-yl) - benzamide, melted at 198 ° C.
PRI me R 9. Act the same as specified in example 1, however, as the starting substances use of 13.4 g of benzoic acid, 17.8 g of N, N -carbonyldiimidazole and 12.3 g of 2-amine-7-methoxy -1,8-naphthyridine. The compound obtained by precipitation in water (20 g, mp) is dissolved in 200 cm of boiling acetonitrile.
thirty
35
40
After 1 h of cooling at 4 ° C
the crystallized solid is separated by filtration, washed twice with 10 cm of acetonitrile and dried at 40 ° C under reduced pressure.
g (0,067 kPa). 7.8 g of H- (7-metroxy-1,8-naphthyridin-2-yl) benzamide are obtained, melting at 134 ° C.
Example 10. They act similarly to that indicated in Example 1, however, 8.9 g of benzoic acid and 11.8 g of N, N -carbonyldiimidazole and 15 g of 2-amine-7-benzylthio-1.8 are used as and; like substances; -naphthyridine. The compound obtained by precipitation in
gg water (25 g, mp) is purified by chromatography on a column having a diameter of 5 cm, containing 600 g of silica (0.063-0.2 mm), eluting with methylene chloride. Collect fractions
50
Shchogos at 95 C.
Example 8. To a solution of 5.4 g of 2-amine-7-chloro-1,8-naphthyridine in 60 cm of pyridine was added slowly 4.2 g of benzoyl chloride, maintaining the temperature at about. After keeping the solution for 3 hours at a temperature of about 20 ° C, the compound is precipitated at 340 cm distilled cyclohexadiene-1-carboxamide, melting
bathroom water. After drying in air, the solid obtained is dissolved in 88 cm of boiling ethanol. After 3 hours of cooling with the crystallized solid, it was separated by filtration, washed with 2 times 5 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa), thus obtaining 4.95 g of N- (7-hlop-1, 8-naphthyridin-2-yl) - benzamide, melted at 198 ° C.
PRI me R 9. Act the same as specified in example 1, however, as the starting substances use of 13.4 g of benzoic acid, 17.8 g of N, N -carbonyldiimidazole and 12.3 g of 2-amine-7-methoxy -1,8-naphthyridine. The compound obtained by precipitation in water (20 g, mp) is dissolved in 200 cm of boiling acetonitrile.
40
After 1 h of cooling at 4 ° C
the crystallized solid is separated by filtration, washed twice with 10 cm of acetonitrile and dried at 40 ° C under reduced pressure.
g (0,067 kPa). 7.8 g of H- (7-metroxy-1,8-naphthyridin-2-yl) benzamide are obtained, melting at 134 ° C.
Example 10. They act similarly to that indicated in Example 1, however, 8.9 g of benzoic acid and 11.8 g of N, N -carbonyldiimidazole and 15 g of 2-amine-7-benzylthio-1.8 are used as and; like substances; -naphthyridine. The compound obtained by precipitation in
g water (25 g, mp) is purified by chromatography on a column having a diameter of 5 cm, containing 600 g of silica (0.063-0.2 mm), eluting with methylene chloride. Collect fractions
0
51
in an amount of 100 cm, fractions 1A-56 are concentrated dry under reduced pressure (4 kPa) to give 22, A g of solid, melting at 142-144 ° C. This compound is dissolved in 250 cm of boiling ethanol. After 2 hours of precipitation at 4 ° C, the crystallized solid is separated by filtration, washed twice with 25 cm of ethanol and dried at 40 s under reduced pressure (0.067 kPa). 19 g of H- (7-benzSH1TIO-1,8-naphthyridin-2-yl) ben3amide are obtained, melting at 144-145 ° C.
2-Amin-7-benzylthio-1,8-naphthyridine can be obtained as follows
To a solution of sodium ethylate, prepared from 2.3 g of sodium and 160 cm-ethanol, add 13.6 g of benzmer-captan and stir for 1 hour at a temperature of approximately 20 ° C. Then 18 g of 2-amine-7-chloro-1,8-naphthyridine are added and heated for 6 hours at. The resulting suspension is poured into 500 cm of water and extracted 250 times with methylene chloride 250 times. After washing with water and drying, the organic solution is concentrated dry under reduced pressure (4 kPa) with the formation of 15.4 g of 2-amine-7-benz1-thio-1,8-naphthyridine melting at 167 C.
Example 11. To a solution of 6.8 g of benzoic acid in 180 cm of anhydrous tetrahydrofuran was added 9.1 g of N., N -carbonyldiimidazole. Note the immediate gas gassing. The mixture is stirred for 2 hours at a temperature approximately equal to the end of the evolution of gas. Then 10 g of 2-amine-7-phenBxy-1,8-naphthyrndine are added and the mixture is heated at reflux for 18 h.
The mixture is poured into 800 cm of distilled water, the precipitate formed is separated by filtration, washed with water and air dried. ,
The resulting compound (14 G5T.pl.) is dissolved in 160 cm of boiling acetonitrile. After cooling for 2 hours at 4 ° C, the crystallized solid is separated by filtration, washed twice with 8. cm of acetonitrile and dried at 25 ° C under reduced pressure (0.067 kPa). 8 g of N- (7-phenoxy-1,8-naphthyridin-2-yl) benzamide are obtained, melting at 170 ° C,
77976
Example 12. They act in the same way as in Example 1, however, 11 g of benzoic acid, 16.2 g of N, N -carbonyldiimidazole and 26.7 g of 2-amine-7- (4-methoxyphenoxy) -1 are used as starting materials. , 8-naphthyridine. The compound obtained by precipitation in water (30.8 g, so pl. Approx.
d 110 ° C), dissolved in 150 cm of boiling acetonitrile. After cooling for 3 hours at ° C, the crystallized solid is separated by filtration, washed twice with 5 cm of acethos of nitrile and dried at 50 ° C under reduced pressure (0.067 kPa). 24.7 g of (4-methoxyphenoxy) -1.8-naphthyridin-2-yl} benzamide are obtained, melting at 1 71 C.
D) 2-Amin-7- (4-methoxyphenoxy) -1,8-naphthyridine can be obtained as follows.
They are similar to those specified in example 4, however, as the initial
5 substances use 35.8 T 2-amine-7-chloro-1,8-naphthyridine, 99.2 g of 4-methoxy-phenol and 22.4 g of potassium hydroxide in tablets at 85%. After treatment in sodium hydroxide and washing receive
0 52.9 g of 2-amine-7- (4-methoxyphenoxy) - 1,8-naphthyridine, melted at 200 ° C.
Example 13. They act in the same way as in Example 1, however, 11.2 g of 2-fluorobenzoic acid, 12.9 g of N, N -carbonyldiimidazole and 8.9 g of 2-amine-7-chloro-1 are used as starting materials. 8-naphthyridine. The compound obtained by precipitating in water (13.6 g, mp) is dissolved in 450 cm of boiling 1-propanol. After cooling for 3 hours at the crystallized solid, it is separated by filtration, washed three times with 20 cm of 1-propanol and dried at 40 ° C under reduced pressure (0.067 kPa). 8.3 g of N- (7-chloro-1,8-naphthyridine-2-pc) -2-fluorobenzamide are obtained, melting at 222 ° C.
Example 14. They act in the same way as in Example 1, however, 20 g of 3-fluorobenzoic acid, 23 g of N, N -carbonyldiimidazolium and 16.9 g of 2-amine-7-chloro-1,8-naphthyridine are used as starting materials. The compound obtained by precipitation in water (25 g, mp) is dissolved in 230 cm of boiling acetonitrile. After 4 hours of cooling with the crystallized solid, section 5
0
one
It is filtered, washed with 2 times 20 cm of acetonitrile and dried under reduced pressure (0.067 kPa). 21.4 g of N- (7-chloro-1,8-naphthyridin-2-yl) -3-fluorobenz amide, melting at 202 ° C., are obtained.
Example 15. They act in the same way as in Example 1, however, as the starting materials, 11.2 g of 4-fluorobenzoic acid, 12.9 g of N, N -carbonyldiimidazole and 8.9 2-amine-7-chloro-1.8 are used as starting materials. -naphthyridine. The compound obtained by precipitation in water (1A, 3 g, mp. 230 ° C) is dissolved in 800 cm of boiling 2-propanol. After 4 hours cooling at 4 ° C, the crystallized solid is separated by filtration, washing three times
10 cm of 2-propanol and suiat at 40 ° C under reduced pressure (0.067 kPa). 10.3 g of K- (7-chloro-1,8-naphthyridin-2-yl) -4-fluorobenzamide are obtained, melting at 236 ° C.
Example 16. They act in the same way as in Example 1, however, 15.4 g of 4-fluorobenzoic acid, 17.8 g of N, N -carbonyldiimidazole and 15.7 g of 2-amine-1-7-bromo-1.8 are used as starting materials. -naphthyridine The compound obtained by precipitation in water (26.2 g, mp 226 ° C) is purified by filtration on a column having a diameter of 45 mm and containing 3-00 g of silica (0.040-0.063 mm), eluting with pure dichloromethane and thus obtaining fractions in an amount of 100 cm. After concentrating dry, fractions 10-70 at 40 ° C under reduced pressure (4 kPa), 18.5 g of solid are obtained Melting at 22.8 ° C. This compound is dissolved in 600 cm of boiling ethanol. After cooling for 2 hours at 4 ° C







172 C. 12 g of L- (7-methoxy-1, 8-naphthyridin-2-yl) -3-acetoxybenzamide, obtained under the conditions indicated above, is treated by heating
crystallized substance separation (0.067 kPa). Get 5,3-g
filter, wash 10 cm of N- (7-MeTOKCH-1,8-naphthyridin-2-yl) -3 ethanol and dry at 40 ° C with reduced acetoxybenzamide, melting at
nominal pressure (0,067 kPa). Get
13.1 g of N- (7-6poM-1,8-naphthyridin-2-yl) 4-fluorobenzamide, melted at QQ
.
Example 17. Operate analogously at reflux for
according to Example 1, but 15 minutes in 35 cm of 10% ethanol
used as the initial ve-solution of potassium hydroxide. Formations 12.1 g of 2,6-difluorobenzoic acid-solid solid after dilution, 12.3 g of N, N -carbonyldiimidazolium 250 cm of water and acidification of 20 cm
and 8.5 g of 2-amine-7-chloro-1,8-naphthyrid-4 n. hydrochloric acid is dried on
on. The compound obtained during the precipitation of air with the formation of 9.2 g of solid
Scientific research institutes in water (6.8 g, mp. 215 C) of a plant substance melting at a temperature of 450 cm of bale 1 / f (ethyleol). After 4 hours of cooling with solid crystallized hydrochloride washed 3 times with 15 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa). 7.3 g of N- (7-. chloro-1,8-naphthyridin-2-yl) -2.6 are obtained. - difluoro-benzamide, melted at 2A2 C.
Example 18. They act in the same way as in Prgmer 1, however, 5.1 g of 2,6-difluorobenzoic acid, 5.2 g of N, N -carbonyutdiimidazole are used as starting materials.

and 4.4 g of 2-amine-7-methoxy-1,8-naphthyridine. The compound obtained, when precipitated in water (4.5 g, mp 215-), is dissolved in 70 cm of boiling ethanol. After 1 h of cooling
at 4 ° C, the crystallized solid is separated by filtration, washed with 10 cm of ethanol and dried at 45 ° C under reduced pressure
(0.067 kPa). 3.2 g of H- (7-metroxy-1,8-naphthyridin-2-yl) -2,6-difluorobenzamide, melting, are obtained at 219-220 ° C. Pr-and mep 19. To a solution of 3.5 g 2amin-7-methoxynaphthiridine in 40 cm
pyridine was added 4.4 g of 3-acetoxybenzoyl chloride. The mixture is stirred for 1 h 30 min at a temperature approximately equal to 25 ° C. The resulting suspension was diluted with 400 cm of distilled water and the resulting precipitate was dried in air to form 6.6 g of a solid melting at. This compound is dissolved in 140 cm of boiling ethanol.
After cooling for 3 hours at 4 ° C; the solid that crystallized out was separated by filtration, washed three times with 20 cm of ethanol and dried at 50 ° C under reduced pressure. 172 ° C. 12 g of N- (7-methoxy-1, 8-naphthydidin-2-yl) -3-acetoxybenzamide, prepared under the conditions indicated above, is treated by heating
acetoxybenzamide, melted at
9 141779710
re, exceeding 260 C. The resulting yield in 660 cm of boiling acetonitrile.
The substance is dissolved in 1500 cm of boiling-water. After 3 hours cooling, the wire is 1-pronanol. After cooling, carried out at 4 ° C, crystallized
stacked for 4 hours at 4 ° C, the solid is separated by filtering the crystallized substance from -three, washed three times in 20 cm
divided by filtration, washed three times with addetonitrile and dried at 50 ° C with 50 cm of 1-propanol was allowed to dry and dried under reduced pressure (0.067 kPa). 6 g of K- (7-label Si-1,8-naphthyridin-2-yl) -3-hydroxybenzamide, m.p.
Example 20. They act in the same way as in Example 1, however, as the starting materials, 4.55 g of 4-methoxybenzoic acid, 6.55 g of H, N -carbonated diimidazole and 5.2 g of 2-amine-1,8-naphthyridine are used. Connection
ten
lower pressure (0,067 kPa). 3.5 g of N- (7-chloro-1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at.
Example 23. The effect is the same as in Example 1, however, 10.2 g of 4-methoxybenzoic acid, 10.8 g of N, N -carbonyldiimidazole and 11.2 g of 2-amine-7-bromo-1 are used as starting materials, 8-naphthyridine. The compound obtained by precipitation in water (9.8 g, mp. 220 ° C),
Obtained by precipitation in water (8.5 g, so pl., paste-like solution is dissolved in 1000 cm of boiling acetone), filtered, then nitrile. After 2 hours cooling.
dissolved in 50 cm of boiling 1-propanol. After 1 hour of cooling at 4 ° C, the solid that crystallized out was separated by filtration, washed twice with 5 cm of 1-propanol and dried at 35 ° C under reduced pressure (0.067 kPa). 6.9 g of N- (1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at 150 ° C.
2-Amine-1,2-naphthyridine can be obtained in accordance with known methods.
Example 21: Acting analogously at 4 ° C., the crystallized solid is separated by filtration, then it is washed twice with 10 cm of acetonitrile and dried at. 40 ° С under reduced pressure (0.067 kPa). 8.3 g of N- (7-bromo-1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at 221 ° C.
Example 24. They act in the same way as in Example 1, however, 12.2 g of 4-methoxybenzoic acid, 10.3 g of K, L-carbonyldiimidazole and 9.5 g of 2-amine-7-methyl-1.8 are used as starting materials. - oil 30
Gichno specified in example 1, however, 35 Dina. The compound obtained by
precipitated in water (14.4 g, mp. dissolved in 150 cm of boiling ac nitrile. After cooling for 2 hours at 4 ° C, the solid crystallized substance was separated by filtration, after which it was washed twice in 10 cm of acetone la and dried at 45 ° C under reduced pressure (0.067 kPa). Get 12
12.17 g of 3-methoxy benzoic acid, 12.9 g of N, N -carbonyl diimidazole and 8.9 g of 2-amine-7-chloro-158-naphthyridine are used as starting materials. The compound obtained by precipitation with water (15.5 g, mp. 176 ° C) is dissolved in 500 cm of boiling 2-propanol. After 2 hours of cooling at 4 ° C, solid screen
Precipitated in water (14.4 g, m.p. IIO, dissolved in 150 cm of boiling aceto-nitrile. After cooling for 2 hours at 4 ° C, the solid crystallized substance was separated by filtration, after which it was washed twice in 10 see acetonitral and dried at 45 ° C under reduced pressure (0.067 kPa). 12.7
the Talizum substance is separated by pu- 45 M-, (7-methyl-1,8-naphthyridin-2-yl) -4- filtration, it is washed three times with methoxybenzamide, melted at 25 cm 2-propanol and dried at 199 WITH.
 under reduced pressure
at low (0,067 kPa). 11.2 rN- (7-chloro-1,8-n aftiridin-2-yl) -3 methoxybenzamide, melting at 178 ° C, is produced
Example 22. They act in the same way as in Example 1, however, Example 25 is used. However, 9.1 g of 3-methoxybenzoic acid, 9.7 g of N, N are used as starting materials. -carbonyl diimidazole 7 g 2-amine-7-methoxy-1,8-naphthyridine
4.6 g of 4-methoxybenzoic acid are 55 Compound obtained by precipitating you, 4.9 g of N, N -carbonyl diimidazole and 3.6 g of 2-amine-7-chloro-1,8-naphthyridine. The compound obtained by precipitation in water (4.3 g, mp), a solution in water (13 g, mp approx. 75 ° C), is dissolved in 90 cm of boiling acetonitrile. After 3 h of cooling, carried out at 4c, solid crystallization
lower pressure (0,067 kPa). 3.5 g of N- (7-chloro-1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at.
Example 23. The effect is the same as in Example 1, however, 10.2 g of 4-methoxybenzoic acid, 10.8 g of N, N -carbonyldiimidazole and 11.2 g of 2-amine-7-bromo-1 are used as starting materials, 8-naphthyridine. The compound obtained by precipitation in water (9.8 g, mp. 220 ° C),
dissolved in 1000 cm of boiling acetonitrile. After 2 hours cooling.
carried out at 4 ° C, the crystallized solid is separated by filtration, then it is washed twice with 10 cm of acetonitrile and dried at. 40 ° С under reduced pressure (0.067 kPa). 8.3 g of N- (7-bromo-1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at 221 ° C.
Example 24. They act in the same way as in Example 1, however, 12.2 g of 4-methoxybenzoic acid, 10.3 g of K, L-carbonyldiimidazole and 9.5 g of 2-amine-7-methyl-1.8 are used as starting materials. -naftiri0
35 dynes The compound obtained by
40
Precipitation in water (14.4 g, mp) is dissolved in 150 cm of boiling acetonitrile. After cooling for 2 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed twice in 10 cm of acetonitrile and dried at 45 ° C under reduced pressure (0.067 kPa). Get 12.7 g
45 M -, (7-methyl-1,8-naphthyridin-2-yl) -4-methoxybenzamide, melted at 199 C.
Example 25: The procedure is the same as in Example 1, however, 9.1 g of 3-methoxybenzoic acid, 9.7 g of N, N -carbonyl diimidazole and 7 g of 2-amine-7-methoxy-1,8- naphthyridine.
The compound obtained during the deposition
in water (13 g, mp. approx. 75 ° C), dissolved in 90 cm of boiling acetonitrile. After cooling for 3 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed 3 times with 10 cm of acetonitrile and dried at 50 ° C under reduced pressure (u, 067 kPa). 8.7 g of N- (7-. Methoxy-1,8-naphthyridin-2-yl) -3-methoxybenzamide are obtained, melting at.
Example 26. Act as described in Example 1, however, about IQ, 13.2 g of 4-methoxybenzoic acid, 14.1 g of N, N -carbonyldiimidazole and 11.5 g of 2-amine-7- methoxy-1, 8-naphthyridine. The compound obtained by g precipitating in water is dried under reduced pressure (0.067 itna) and
cleaned by filtration in a column having a diameter of 5 cm, containing
400 g of silica (0.063-0.2 mm) 2 ° The doy is separated by filtration.
washed twice with 10 cm of diethyloxide and dried at 40 ° C. under reduced pressure (0.067 kPa). 12.9 g of N- (7-isopropoxy-1,8-naphthyridine-2 using methylene chloride as eluent are obtained. Fractions of 100 cm are obtained. Fractions 8-38 are combined and concentrated to dryness under reduced pressure (4 kPa). Received soy-25 yl) -4-methoxybenzamide, melting
The mixture is dissolved in 150 cm of boiling acetonitrile. After 4 hours of cooling at 4 ° C, the solid that crystallized out was separated by filtration, then washed twice with 10 cm of acetonitrile and dried at 40 ° C under reduced pressure (0.067.CPa).
10, .9 g of L- (7-metxy-1,8-naphthyridin-2-yl) -4 methoxybenzamide are obtained, melting at 115 C.
2-Amine. -7-methoxy-1,8-naphthyridine- can be prepared according to a known procedure.
PRI mme. 27. Act as in Example 1, however, 19.8 g of 4-methoxybenzoic acid, 21.1 g of N, N -carbonyldiimidazole and 18.5 g of 2- amine-7-ztoxy-1,8-naphthyridine. The compound obtained by precipitation in water (28.9 g., M.p. 144 ° C) is dissolved in 2NW cm of boiling ethanol. After 3 hours of cooling at 4 ° C, the crystallized solid is separated by filtration, then it is washed twice with 10 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPi). 24 tons of N- (7-3TOKCH-1,8-naphthyridin--2-yl) -4-methoxybenzamide, melting at 152 C. are obtained.
.
Iq
g
1779712.
Example 28. They act in the same way as in Example 1, but use: 16.7 g of methoxybenzoic acid I as starting materials.
lots, 19.4 g of N, N -carbonyldimidazole and 25 g of 2-amint7-isopropoxy-1,8-naphthyridine. The reaction mixture was poured into water and extracted with ethyl acetate. After concentrating dry under reduced pressure (4 kPa), the resulting oil (39 g) is stirred in the presence of 100 cm of diethyloxide to form a crystalline solid (23 g, mp. 78 ° C). The resulting compound is dissolved in a boiled isopropyl oxide. After cooling for 2 hours at 4 ° C, the solid which crystallized out was separated by filtration.
washed twice with 10 cm of diethyloxide and dried at 40 ° C. under reduced pressure (0.067 kPa). 12.9 g of N- (7-isopropoxy-1,8-naphthyridine-2 at 82 ° C are obtained. C.
2-amino-7-isopropoxy-1,8-naphthyri-, dyne can be obtained in the following way. Q They act in a manner similar to that specified in Example 28, however, -35.9 g of 2-amine-7-chloro-1,8-naphthyridine, 150 cm of 2-propanol and 9.2 g of sodium are used as starting materials. The excess 2-propanol is evaporated under reduced pressure (4 kPa), and the residue is dissolved in distilled water in order to obtain a solid crystalline substance (38.7 g, mp 162 ° C), 11 g of the obtained solid substances are dissolved. in 50 cm of boiling ethyl acetate. After cooling for 2 hours at 4 ° C, the crystallized solid substance is separated by filtration, washed with 2 times 5 cm of diethyloxide and dried at 50 ° C under reduced pressure (0.067 kPa). 6.9 g of 2-amine-7-isopropoxy-1,8; -naphthyridine are obtained, melting at
0
five
0
.
Example 29. They act in the same way as in Example 1, however, 5.8 g of 4-J methanol syrupol acid, g 6.5 g of N, N -carbonyldiimidazole and 8.5 g of 2-amine-7- (2 -methoxyethoxy) -1,8-naphthyridine. The compound obtained by precipitation in water (8 g, mp. 75 ° C, pasty) is purified by chromium13
The photographs on a column having a diameter of 40 mm, containing 250 g of silica (0.063-0.2 mm), were eluted with a mixture (99.5-0.5 by volume) of methylene chloride and methanol. The fractions are collected in an amount of 100 cm, while the fractions 12-31 are combined and concentrated to dryness under reduced pressure (4 kPa) at. With obtaining 10.3 g of a solid substance, melting at 114 ° C. This compound is then dissolved in 50 cm of boiling carbon tetrachloride. After 16 h of cooling, produced at 4 ° C, cure-15 and dried under reduced pressure (0.067 kPa). 8.9 g of K- (7-allyloxy-1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at
The lysated solid is separated by filtration, then it is washed with 2 times 5 cm of carbon tetrachloride and dried at 40 ° C under reduced pressure (0.067 kPa). 8.5 g of N-7- (2-methoxyethoxy) -1,8-naphthyridin-2-yl) -4-methoxybenzamide 5 are obtained, melting at 114 ° C. .
2-Amin-7- (2-methoxyethoxy) -1,8-naphthyridine can be obtained barely. blowing way.
Alcohol 2-methoxyethanol semi-. from 100 cm of the corresponding alcohol and 9.2 sodium. When the evolution of gas has ended, 35.9 g of 2-amine-7-xpor-1,8-naphthyridine are added, after which the reaction mixture is stirred at 120 ° C for 2 hours and 30 minutes and then poured; (after cooling) in 100 cm of water. The resulting solid is filtered and dried in air (30 g, mp 175 ° C), 10 g of the compound obtained is dissolved in 175 cm of boiling 2-propanol. After 3 hours cooling at 4 ° C, the crystallized solid is separated filtering, rinse it in 10 cm of 2-propanol, and dry at 50 ° C under continuous pressure (0.067 kPa). 8.9 g of 2-amine-7- (2-methoxy-ethoxy) -1,8-naphthyridine are obtained, melting at 17 6 ° C.
20
25
thirty
35
40
108 C.
2-Allyloxy-7-amine-1,8-naphthyridine can be obtained as follows. I Act similarly to that specified in Example 29; however, 17.9 g of 2-amine-7-HLRP-1,, 8-naphthyridine, 75 cm of allyl alcohol and 5.6 g of sodium are used as starting materials.
After the reaction mixture was poured into water, 17.6 g of crystallized solid, melting at 138 ° C, were obtained, 7 g of the obtained compound was dissolved in 210 cm of boiling carbon tetrachloride. After cooling for 3 hours at 4 ° C, the crystallized solid is separated by filtration, after which it is washed three times with 10 cm of carbon tetrachloride and dried under reduced pressure (0.067 kPa). 6.4 g of 2-allyloxy-7-amine-1,8-naphthyridine are obtained, melting at 138 ° C.
. Example 31. They act in the same way as in Example 1, using the same material as starting materials, using 45 WT 11.5 g of 4-methybenzoic acid, 12 g of K, K-carbonyldiimidazole, and 10 g of 2-amine-7-propargyloxy-1.8 -naphthyridine. Compound, obtained by precipitation in water (15.3 g, m.p.
. Example 31. They act in the same way as in Example 1, using as their starting materials 45 WT 11.5 g of 4-methoxybenzoic acid 12 g K, K-carbonyldiimidazole and 10 g 2-amine-7-propargyloxy-1,8- naphthyridine. Compound, obtained by precipitation in water (15.3 g, m.p.
Example 30. They act in the same way as in Example 1, however., As the starting materials used, dissolved in 190 cm, boiling 9.6 g of 4-methoxybenzoic acid, 10.2 g of N, N - carbonyldiim idazole and 8.5 g of 2-allyloxy-7-amine-158-naphtigo ethanol. After 3 hours of cooling at 4 ° C, the solid that crystallized out was separated by filtration, washed 3 times with 20 cm of ethanol and dried at 50 ° C under reduced pressure (kPa). 10.1 g of K- (7-propargyloxy-1,8-naphthyridin-2-yl) -4-methoxybenz-amide are obtained, melting at 140 ° C.
readin The compound obtained by precipitation in water (13.9 g, mp. Approx.) Is purified by chromatography on a column having a diameter of 40 mm, containing 250 g of silica (0.040-0.063 mm), os
141779714
elution with a mixture (99-1 by volume)
methylene chloride and methanol. Collect fractions in an amount of 100 cm while fractions 9-23 are combined and concentrated dry at 40 ° C under reduced pressure (4 kPa) to obtain 10 g of a fatty solid. This compound is dissolved in 50 cm of isopropoxide. After 30 minutes of stirring at 20 ° C, the crystallized solid is separated by (filtration, then it is washed twice with 10 cm of isopropyloxide
and dried under reduced pressure (0.067 kPa). 8.9 g of K- (7-allyloxy-1,8-naphthyridin-2-yl) -4-methoxybenzamide are obtained, melting at
108 C.
2-Allyloxy-7-amine-1,8-naphthyridine can be obtained as follows. I Act similarly to that specified in Example 29; however, 17.9 g of 2-amine-7-HLRP-1,, 8-naphthyridine, 75 cm of allyl alcohol and 5.6 g of sodium are used as starting materials.
After the reaction mixture was poured into water, 17.6 g of crystallized solid, melting at 138 ° C, were obtained, 7 g of the obtained compound was dissolved in 210 cm of boiling carbon tetrachloride. After cooling for 3 hours at 4 ° C, the crystallized solid is separated by filtration, after which it is washed three times with 10 cm of carbon tetrachloride and dried under reduced pressure (0.067 kPa). 6.4 g of 2-allyloxy-7-amine-1,8-naphthyridine are obtained, melting at 138 ° C.
Example 31. They act in the same way as in Example 1, one at a time as starting materials using WT 11.5 g of 4-methybenzoic acid, 12 g of K, K-carbonyldiimidazole and 10 g of 2-amine-7-propargyloxy-1,8- naphthyridine. Compound, obtained by precipitation in water (15.3 g, m.p.
The dye is dissolved in 190 cm of boiling water and the solvent is dissolved in 190 cm of boiling ethanol. After 3 hours of cooling at 4 ° C, the solid that crystallized out was separated by filtration, washed 3 times with 20 cm of ethanol and dried at 50 ° C under reduced pressure (kPa). 10.1 g of K- (7-propargyloxy-1,8-naphthyridin-2-yl) -4-methoxybenz-amide are obtained, melting at 140 ° C.
2-Amin-7-propargyloxy-1,8-naphthyridine can be prepared as follows.
The procedure is the same as in Example 29; however, 179 g of 2 amine-7-chloro-1,8-naphthyridine, 750 cm of propargyl alcohol and 46 g of sodium are used as starting materials. After precipitation in water, rubber (120 g) is obtained, which is dissolved in 500 cm of isopropyl oxide with stirring. The solid obtained (114.5 g, mp. Approx. 150 ° C) is purified by chromatography on a column having a diameter of 5 ohms, containing 1 kg of silica (0.063-0.2 mm), eluted with methylene chloride to obtain fractions in an amount of 100 cm (fractions 11-20), and then fractions 21-26 in an amount of 500 cm. After concentrating dry 6-26 under reduced pressure (4 kPa), the resulting residue is rinsed while moving with ethyl ether, filter m, and then dried. Get 21 VA,
this compound is dissolved in 100 boiling acetonitrile. After 3 hours ohg of solid substance I, melted at 184 C, 10.8 g
cm
at the time of you
the crystallized solid is separated by filtration, washed three times with 20 cm of acetonitrile and existing at 40 ° C under reduced pressure (0.067 kPa). 6.8 g of 2-amine-7-propargyloxy-1,8-naphthyridine are obtained.
Example 32. They act in the same way as in Example 1, however, 11.8 g of 4-methoxybenzoic acid are used as starting materials.
lots, 12.6 g N, N -carbonyldiimidazole and 9.6 g 2-amine-7-methylthio-1,8-naphthyridine. The resulting compound is dissolved in water (15.8 g, mp 100 ° C) in 180 cm of boiling 2-propanol. After 1 hour of cooling, carried out at 4 ° C, the crystallized solid is separated by filtration, washed with 10 cm of 2-propanol, then twice 10 cm of isopropyl oxide and existed at 40 ° C under reduced pressure (0.067 kPa). 13.6 g of N- (7-methylthio-1,8-naphthyridine-2-yl) -4-methoxybenzamide are obtained, melting at 130 ° C.
2-methylthio-7-amine-1,8-naphthyridine can be prepared as follows.
To a solution close to saturation, methylmarcaptan in 200 cm dimethyl
0
five
formamide, maintained at 0 ° C, 13.3 g of sodium hydride are added in small doses as a 50% suspension in mineral oil in small doses. Then, 25 g of 2-amine-7-chloro-1,8-naphthyridine was added to this solution and the mixture was heated at 100 ° C for 2 hours. After cooling, the reaction mixture was drunk in 500 cm of water and extracted 5 times with 250 cm of methylene chloride . The organic extracts are then washed with 2 times 200 cm of distilled water, dried over magnesium sulphate and g is concentrated dry at 40 ° C under reduced pressure (4 kPa). The resulting compound (22.9 g, t.p. 130 s) is dissolved in 150 cm of boiling ethanol. After cooling for 2 hours at ° C, the solid that crystallized out was separated by filtration, then washed with 10 cm of ethanol, and then –3 times 10 cm of isopropyl oxide, and then dissolved at 40 ° C under reduced pressure (0.067 kPa). 9.6 g of 2-amine-7-methylthio-1,8-naphthyridine are obtained, melting at 158 ° C.
Example 33. They act in the same way as in Example 1, however, 4.1 g of 4-methoxybenzoic acid, 4.4 g of K, K -carbonyldiimidazole are used as starting materials. and 4.75 g of 2-amine-7-phenoxy-1,8-naphthyridine. The compound obtained by precipitation in water (8.8 g) is purified by column chromatography having 5
0
diameter of 3 cm, containing 140 g
silica (0,, 2 mm), elution with a mixture (99-1 by volume) of methylene chloride and ethyl acetate. The fractions are collected in an amount of 50 cm, while the fractions 7-20 are combined and concentrated to dryness at 40 ° C under a reduced pressure (4 kPa) to obtain 5.9 g of a solid substance, melting at a temperature equal to 150 ° C. This compound is dissolved in 70 cm of boiling ethanol. After cooling for 2 hours at 4 ° C, the solid that crystallized out was separated by filtration, washed twice with 10 cm of ethanol and dried under reduced pressure (0.067 kPa). 10 g of K- (7-phenoxy-1,8-naphthyridin-2-ip) -4-methoxybenzamide are obtained, melting at 160 C.
Example 34. They act in the same way as in Example 1, however, 6.1 g of 4-methoxybenzo1 {Noah acid, 6.5 g of N, N -carbonyldnnmidazole and 7.65 g of 2-amine-7- ( 2-fluoropheioxy) -1,8-naphthyridine. The compound obtained by precipitation in water (5.5 g, t.L.) is dissolved in 180 cm of boiling ethanol. After cooling for 2 hours, the solid that crystallized out was separated by filtration, washed 2 times with 10 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa). 3.8 g of H-.7- (2-fluorophenoxy) -1,8-naphthyridin-2-yl-4-methoxybenzamide are obtained, melting at 208 ° C.
2-amine-7- (2-fluorophenoxy) -1,8-naphthyridine can be obtained as follows.
They act in the same way as in example 37, however, 18 g of 2-amine 7-chloro-1,8-naphthyridine, 44.8 g of 2-fluorophenol and 13.2 g of potassium hydroxide in tablets by 85% are used as starting materials, with sodium hydroxide and washing, the resulting compound (24 g, mp. 202 ° C) is dissolved in 200 cm of boiling ethanol. After cooling for 4 hours at 4 ° C, the crystallized solid is separated by filtration, washed twice with 15 cm: ethano. la and dried under reduced pressure (0.067 kPa). 14.9 g of 2-amine-7- (2-fluorophenoxy) are obtained. - 1,8-naphthyri dine, melting at 206 C. Example 35. Actually ordered in Example 1, however, 6.1 g of 4 methoxybenzyl acid, 6.5 g of N, N -carbonyldiimidazole and 7.65 g of 2-a o1n-7 - (3 fluorophenodsyl) -1 are used as starting materials , 8- naphthyridine. The compound obtained by precipitation in water (14 g) is dissolved in 100 cm of boiling ethanol. After cooling for 2 hours at 4 ° C, the solid that crystallized out was separated by filtration, then washed twice with 10 cm of ethanol and dried at 45 ° C under reduced pressure (0.067 kPa). 7 g of (3-fluorophenoxy) -1,8-naphthyri-DYN-2-IL-4-methoxybenzamide are obtained, melting at 151 C.
2-Ami} 1-7- (3-fluorophenoxy) -1,8-naphthyridine can be obtained in the following manner.
They act in the same way as in Example 37, however, 18 g of 2-amine-7-chloro-1,8-naphthyridine, 44.8 g of 3-fluorophenol and 13.2 g of potassium hydroxide in tablets are 85% used as starting materials. . After treatment with sodium hydroxide and washing, the resulting compound (23.5 g, so pl.
161 ° C) is dissolved in 120 cm of boiling acetonitrile. After a 2-hour oh-,. At 4 ° C, the solid that crystallized out was separated by filtration, washed twice with 1.0 cm of acetonitrile and dried under reduced pressure (0.067 kPa). 16.5 g of 2-amine-7- (3-fluorophenoxy) -1.8 naphthyridine are obtained, melting at 165 s. Example 36. Anapogically indicated in Example 1, however, 14.3 g of 4-methoxybenzoic acid, 15.2 g of NjN -carbonyldiimidazole and 15.2 g of 2-amine-7- (4-fluorophenoxy) - 1.85 naphthyridine. The compound obtained by precipitation in water (22.6 g, mp. Approx. 70 ° C) is dissolved in 130 cm of boiling ethanol. After cooling for 3 hours at 4 ° C, the solid crystallized substance is separated by filtration, washed twice with 15 cm of ethanol and dried at 25 ° C under reduced pressure (0.067 kPa). 17 g of N- t 7- (4-fluorophenoxy) -1,8-naphthyridin-2-yl-4-methoxybenzamide are obtained, melting at 100 ° C.
2-AMIN-7- (4-fluorophenoxy) -1,8-naphthyridine can be obtained as follows.
The procedure is the same as in Example 4, however, 17.9 g of 2-amine-7-HLOR-1,8-naphthyridine, 44.8 g of 4-fluorophenol and 13.2 g of potassium hydroxide are used as starting materials. tablets of 85%. After 2 hours
5 heating, carried out during processing and processing, similarly specified. Example 4, get 15.2 g of 2-amine- - (4-fluorophenoxy) -1,8-naphthyridine, melt at 210 ° C.
0
Example 37: The procedure is the same as in Example 1; however, 16.4 g of 4-methoxybenzoic acid, 17.5 g of N, N -carbonyldiimidazole and 18.5 g of 2-amine-7- (2 -chlorophenoxy) - 1,8-naphthyridine. The compound obtained by precipitation in water (28 g, mp. At SL. 80 C) is dissolved in
five
0
80.0 cm of boiling ethanol. After cooling for 15 hours at 4 ° C, the solid that crystallized out was separated by filtration, washed twice with 20 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa). 17.8 g of N-t7- (2 chlorophenoxy) -1,8-naphthyridin-2-yl3-4 are obtained.
methoxybenzamide, melting point 190 ° C.
2-Amin-7- (2-chlorophenoxy) -1,8-naphthyridine can be obtained as follows.
A mixture of 17.9 g of 2-amine-7-chloro-1,8-naphthyridine, 51.4 g of 2-chlorophenol and 13.2 g of potassium hydroxide in tablets is heated for 4 hours at 120 ° C. by 85%. The resulting mixture is extracted into 100 cm 4 n sodium hydroxide, the precipitate formed is separated by filtration, then washed with water until pH 7 is reached. After drying at 40 ° C under reduced pressure (0.067 kPa), 20.6 g are obtained. 2-amine- 7- (2-chlorophenoxy) -1,8-naphthyridine, melted at 166 ° C.
Example 38. Act similarly to that specified in Example 1, however, 9.7 g of 4-methoxybenzene acid, 10.4 g of N, N -carbonyldiimidazole and 12.4 g of 2-amine-7 are used as starting materials. - (2-bromophenoxy) - 1,8-naphthyridine. The compound obtained by precipitation in water (17.6 g, mp. Approx. 70 ° C) is purified by chromatography on a column having a diameter of 45 mm, containing 250 g of silica (0.040-0.063 mm), by elution with a mixture ( 99-1 by volume) of methylene chloride and methanol, while collecting these fractions in an amount of 50 cm. After concentration on dry fractions for 5-1 7 minutes at 40 ° C under reduced pressure (4 kPa), 10.4 g of a solid substance are obtained, melting at a temperature of approximately 70 ° C. This compound is dissolved in 270 cm. Of boiling ethanol. After cooling at 4 ° C for 3 hours, the crystallized solid is separated by filtration, then it is washed with 2 times 15 cm of ethanol and dried under reduced pressure.
(0.067 kPa). 8.8 g of N-t7- (2-bromophenoxy) -1.8-1 naphthyridin-2-yl3-4-methoxybenzamide are obtained, melting at
.
2-Lmin-7 (2.-bromophenoxy) - 1, 8-naphthyridine can be obtained as follows.
The procedure is the same as in Example 4; however, 19.7 g of 2-amine 7-chloro-1,8-naphthyridine, 81.5 g of 2-bromophenol and 15.15 g of potassium hydroxide in tablets of 85% are used as starting compounds. After 10 hours of heating, carried out at 120 ° C, and treatment under conditions similar to those indicated in Example 4, the resulting compound (21.5 g, mp 160 ° C) is purified by chromatography on a column having a diameter of 45 mm, containing 300 g of silica (0.040-0.063 mm), —eating with a mixture (95–5 by volume) of methylene chloride and methanol, collecting fractions in an amount of 100 cm. After concentrating dry, a fraction of 2–10 at 40 ° C and under reduced pressure (4 kPa), 12.8 g of 2-amine-7- (2-bromophenoxy) -1.8-naphthy 206 0 are obtained.
dina melted at
Example 39. The procedure is the same as in Example 1; however, 15 g of 4-methoxybenzoic acid, 16 g of N-, N-carb onyl diimidazole and 15.5 g of 2-amine-7- (2- methylphenoxy) -1,8-naphthyridine. The compound obtained by precipitation in water (19 g, mp 50 ° C) is purified by chromatography on a column having a diameter of 45 mm, containing 270 g of silica (0.040-0.063 mm), by elution with pure dichloromethane. Collect fractions in the amount of 100 cm. After concentrating the dry fractions 3-40, carried out under reduced pressure (4 kPa) and at 40 ° C, 14 g of a solid, melting at about 50 ° C, is obtained. This compound is dissolved in 120 cm of boiling ethanol. After cooling for 4 hours with the solid that crystallized out, it was separated by filtration, after which it was washed with 10 cm
ethanol and dried under and under reduced pressure (0.067 kPa). 11.1 g of K-7-C2-methylphenoxy) -1,8-naphggg tiridin-2-yl-4-methoxybenzamide are obtained, melting point at 153 C.
2-Amin-7- (2-methylphenoxy) -1,8-naphthyridine can be obtained as follows.
The procedure is the same as in Example 4; however, 17.95 g of 2-amine-7-chloro-1,8-naphthyridine, 43.2 g of 2-methylphenol and 13.2 g of potassium hydroxide in tablets of 85% are used as starting materials. . After treatment with sodium hydroxide and washing, the resulting compound (21.2 g, mp) is dissolved in 100 cm of boiling acetonitrile. After cooling for 4 hours, the crystallized substance is separated by filtration, after which it is washed with 10 cm of acetonitrile and dried under reduced pressure (0.067 kPa). This gives 2-amine-7- (2-methylphenoxy) -1,8-naphthyridine, melting at 192 ° C.
Example 40. Operate as indicated in example 1, however, c. 8.5 g of 4-methoxybenzoic acid, 9 g of N, N -carbonyldiimidazole and 9 g of 2-amine-7- (3-methylphenoxy) -1,8-naphthyridine are used as starting materials. The compound obtained by precipitation in water (10 g, mp 110 ° C) is purified by filtration through a column having 45 mm in diameter and containing 150 g of silica (0.040-0.063 mm), elution with dichloromethane. thus obtaining fractions in the amount of 100 cm. After concentrating the dry fractions 1-30s carried out at 40 ° C under reduced pressure (4 kPa), 9 g of solid are obtained, melting at. This compound is dissolved in 120 cm of boiling ethanol. After 4 hours cooling at 4 ° C, the solid crystallizing substance is separated by filtration, after which it is washed with 10 cm of ethanol and dried at 40 ° C and under reduced pressure (0.067 kPa). (3-. Methylphenoxy) 1,8-naphthyridin-2-yl-4 methoxybenzamide, m.p. ;
2-Am tsh-7- (3-methylphenoxy) -: 1,8-naphthyridine can be obtained as follows.
They act in the same way as in Example 4, however, 17.95 g of 2-amine-7-chloro-198-naphthyridine, 43.2 g of 3-mWh, phenol and 13.2 g of potassium hydroxide in tablets of 85% are used as starting materials. . After treatment with sodium hydroxide and washing, the resulting compound (21 g, mp. 148 ° C) is dissolved in 200 cm of boiling ethyl acetate. After 18 hours of cooling, the solid crystallized substance is separated by filtration, then it is washed with 10 cm of ethyl acetate and dried at 40 ° C under reduced pressure (0.067 kPa). 9 g of 2-amine-7- (3-methylphenoxy) -1,8-naphthyridine are obtained, melting at 152 C.
Example 41. Operate as specified in example 1, however
16.7 g of 4-methoxybenzoic acid, 17.8 g of N, N -carbonyldiimidazole and 21.2 g of 2-amine-7- (2,6-dimethylphenoxy) -1,8-naphthyridine are used as starting materials. Reaction mixture
poured into water and extracted with methylene chloride. After concentrating the organic phases dry under reduced pressure (4 kPa), the resulting solid (33 g) is dissolved in
170 cm of boiling acetone. After cooling for 2 hours at a solid, the crystallized substance is separated by filtration, after which it is washed with 10 cm of acetone and dried at
40 ° C under reduced pressure
(0.067 kPa). By recrystallization of the obtained solid (11.5 g, mp. Approx. 100 ° C), carried out in 50 cm of acetone, 9.1 g (2,6-Dimethylphenoxy) -1,8-naphthyridine are obtained. -2-yl3-4 methoxybenzamide, melted at 174 C.
2-Amin-7- (2,6-dimethylphenoxy) -1,8-naphthyridine can be obtained as follows.
The procedure is the same as in Example 4; however, 17.95 g of 2-amine-7-chloro-1, 8-naphthyridine, 48.6 g of 2,6-dimethylphenol and 13.2 g of potassium hydroxide in tablets per 85%. After treatment with sodium hydroxide and washing, the resulting compound (24.8 g, so pl.
204 ° C) is purified by chromatography on a column having a diameter of 45 mm, containing 360 g of silica (0.040-0.063 mm), elution with pure methylene chloride and obtaining 100 cm of fraction. After concentrating the dry fractions 1-48, carried out at 40 ° C, under reduced pressure (4 kPa), 21.2 g of 2-amine-7-1 $ 2,6-dime23, 14 are obtained
tilphenoxy) -, 8-naphthyridine, melted at 218 ° C.
Example 4.2. Acts as indicated in Example 1, however, 10.2 g of 3-methoxybenzoic acid, 10.9 g of N, N -carbonyldiimidazole and 13.4 g of 2-amine-7- (2-methoxyphenoxy) 1.8 are used as starting materials. -naphthyridine. The compound obtained by precipitation in water (18 g, mp. 167 ° C) is dissolved in 400 cm of boiling ethanol. After cooling for 2 hours at 4 ° C, the solid which crystallizes out is separated by filtration, then washed twice with 10 cm of ethanol and dried at 45 ° C and under reduced pressure (CO, G67 kPa). 14 g of (2-methoxyphenoxy) -1,8-naphthyridin-2-yl-4-methoxybenzamide are obtained, melting at 168-170 s.
Example 43. They act in the same way as in Example 1, however, 15.9 g of 4-methoxybenzoic acid, 17 g of H, H -carboxylate 1-imidazole and 17.7 g of 2-amine-7- (3-methoxyphenoxy ) - 1,8-naphthnridine. The compound obtained by precipitation in water (12.1 g, mp 14 ° C) is purified by filtration on a column having a diameter of 45 mm, containing 180 g of silica (0.040-0.063 mm), wire isolated with pure dichloromethane, obtained with 100 cm of this fraction. After concentrating dry fractions 1-50, carried out at 40 ° C and under reduced pressure (4 kPa), 10 g of solid are obtained, melting at This compound is dissolved in 130 cm of boiling ethanol. After cooling for 18 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed with .10 cm of ethanol and dissolved at 40 ° C under reduced pressure (0.067 kPa). 9 g of (3-methoxyphenoxy) - i1 8-naphthyridin-2-yl-4-methoxybenzamide, melting at 150 ° C. are obtained.
2-Amin-7- (3-methoxyphenoxy) -1,8-naphthyridine can be obtained as follows.
The procedure is the same as in Example 4; however, 17.95 g of 2-amine-7-chloro-1,8-naphthyridine, 49.6 g of 3-met-hydroxyphenol and 13.2 g of potassium hydroxide in tablets are used as starting compounds. 85%. After processing
17797
24
sodium hydroxide and washing the resulting compound (23.8 g, mp. 156 ° C) is dissolved in 200 cm of boiling ethanol. After cooling for 18 hours, the solid that crystallized out was separated by filtration, after which it was washed with 10 cm of ethanol and
40 C and under reduced pressure
(0.067 kPa). 17.7 g of 2-amine-7- (3-methoxyphenoxy) -1,8-naphthyridine are obtained, melting at 160 ° C.
Example 44. Analogous act.
according to Example 1, however, 9.5 g of 4-methoxybenzoic acid, 10.2 g of N, N -carbonyldiimidazole and 10.7 g of 2-amine-7- (4-methoxyphenoxy) 1, 8- naphthyridine. The compound obtained by precipitation in water (14.3 g, mp. 106 ° C) is purified by chromatography on a column having a diameter of 35 mm and containing 200 g of dioxide
silicon (0.040-0.063 mm), was eluted with a mixture (98-2 by volume) of methylene chloride and methanol, thus obtaining fractions in an amount of 50 cm. Fractions 22-28 were concentrated to dryness.
under reduced pressure (4 kPa) to obtain 10.8 g of a solid melting at 150 ° C. This compound is dissolved in 250 cm of boiling ethanol. After cooling for 3 hours at 4 ° C, the solid that crystallized out was separated by filtration, followed by washing it twice with 10 cm of ethanol and sous. Shat at 40 ° C under reduced pressure
(0.067 kPa). 9 g of (4-Me-. Toxophenoxy) -1,8-naphthyridin-2-yl-4-methoxybenzamide are obtained, melting at 163 ° C.
Example 45. The analogue is valid:
according to Example 1, however, 3.6 g of 4-m-etoxybenzoic acid are used as starting materials. You, 4.05 g of N, N -carbonyldiimidazole and 6.5 g of 2-amine- (3-pyridyl) -7-oxy1, 8-naphthyridine. The compound obtained by precipitation in water (3.9 g, mp. Approx. 110 ° C) is purified by chromatography on a column having a diameter of 25 mm, containing 80 g of silica (0.040-0.063 mm), and see the following: as eluent.methylene chloride and thus obtaining fractions in an amount of 50 cm. Fractions 16-28 are combined and concentrated dry at
.
251417797
pressure (4 kPa) for semi-solid crystallization of tea 7ci
the substance melting at 17 ° C. The isolated compound is dissolved in 125 cm of boiling ethyl acetate. After cooling for 2 hours at 4 ° C, the solid which crystallizes out is separated
by filtration, washed twice with 3 cm of IQ hydroxy-1,8-naphthyridine may be semi-ethyl acetate and dried at 50 ° C with as follows, under reduced pressure (0.067 kPa). 2.5 g of N- (3-pyridyl) -7-hydroxy-1,8-naphthyridin-2-yl-4-methoxybenzamide are obtained,
melt shy at. substances use 27 g of 22-amine- (3-pyridyl) -7-hydroxy-1,8-naph-amine-7-chloro-1,8-naphthyridine, 71 g
The procedure is the same as in Example 29, however, as is 4-hydroxy-1-methylpiperidine and 8 g of sodium. After treatment in water, the reaction mixture is extracted with methylene chloride to obtain 33.4 g of an amorphous solid. The solid is purified by chromatography on a column having a diameter of 60 mm, containing 335 g of silica dioxide 25 (0.040-0.063 mm), is eluted with a mixture (90-10 by volume) of methylene chloride, and methanol, resulting in fractions S in an amount of 100 cm. Frac tiridine can be obtained as follows.
17.9 g of 2-amine-7-chloro-1,8-naphthyridine, 38 g of 3-hydroxypyridine and 11.2 g of potassium hydroxide in tablets are 85%, used as starting materials, but used as starting materials the compound, when convicted in water and extracted with ethyl acetate (4.7 g), is dissolved in 80 cm of boiling ethyl acetate. After 3 hours of cooling, carried out at 4 ° C, you
4-hydroxy-1-methylpiperidine and 8 g of sodium. After treatment in water, the reaction mixture is extracted with methylene chloride to obtain 33.4 g of an amorphous solid. The solid is purified by chromatography on a column having a diameter of 60 mm, containing 335 g of silica dioxide 25 (0.040-0.063 mm), is eluted with a mixture (90-10 by volume) of methylene chloride, and methanol, resulting in S fractions in an amount of 100 cm. Frakushchy 12-35 are concentrated dry at
the crystallized substance 5 ° is separated by a reduced pressure (4 kPa) and obtained by filtration, washed twice with 5 cm.
The addition of 10.4 g of a solid melting at about 100 ° C. This compound is dissolved in 50 cm of boiling cyclohexane. By using 10.4 g of a solid, melting at a temperature of about 100 ° C. This compound is dissolved in 50 cm of boiling cyclohexane. According to the implementation of the simple ethyl ether and dried on the air at. 2.1 g of 2-amine- (3-pyridyl) -7-oxn-1,8-naphthyridine, melting at 178 ° C, are obtained.
Example 46. They act similarly to that specified in Example 1, however, it is used as starting materials. 4.6 g of 4-methoxybenzoic acid, 4.9 g of N, N -carbonyldiimidazole and 5.1 g ... under reduced pressure (0.067 kPa) are used. 2-amine- (1-methyl-4-piperidyl) -7-hydroxy- 453 g of 2-amia- (1-methyl-4-feed for 1 h of cooling, obtained at 4 ° C, are obtained. The solid crystallized by filtration, after which it was washed with 20 cm of cyclohexane and dried at
1,8-naphthyridine. The compound obtained by precipitation in water (6.5 g, i.e. approximately 80 ° C) is dissolved in 100 cm of methylene chloride., The compound
extracted with 100 cm 2 n. hydrochloric acid, and the aqueous phase obtained is washed twice with 50 cm of methylene chloride, and then neutralized with 50 cm 4 n. sodium hydroxide in the presence of 100 cm-methylene chloride. After washing in water and drying, the organic phase is concentrated dry at 40 ° C under reduced pressure (4 kPa) to give 6.3 g of an amorphous compound. This compound is dissolved in 50 cm of boiling methyl 1-1-clohexane. After cooling for 1 hour at 20 ° C, the crystallized substance
26
is separated by filtration, after which it is washed with 20 cm of methylcyclohexane and dried at 50 ° C under reduced pressure (0.067 kPa). 5.6 g of NC (1-methyl-4-steride1) -OXY-1,8-naphthyridine-2-Rp} -4-marks of sibenzamide are obtained, melting at 200 s, 2-Amine- (1-methyl-A -piperidyl) -7oxy-1, 8-naphthyridine can be obtained as follows
Act similar to that specified in example 29, but as isamin-7-chloro-1, 8-naphthyridine, 71 g
0
4-hydroxy-1-methylpiperidine and 8 g of sodium. After treatment in water, the reaction mixture is extracted with methylene chloride to obtain 33.4 g of an amorphous solid. The solid is purified by chromatography on a column having a diameter of 60 mm, containing 335 g of silica dioxide 25 (0.040-0.063 mm), is eluted with a mixture (90-10 by volume) of methylene chloride, and methanol, resulting in S fraction of 100 cm. Fractional pressure (4 kPa) with
The addition of 10.4 g of a solid melting at about 100 ° C. This compound is dissolved in 50 cm of boiling cyclohexane. According to the effect of reduced pressure (0.067 kPa). 453 g of 2-amia are obtained (1-methyl-4-feeding for 1 h, cooled at 4 ° C, the solid crystallized substance is separated by filtration, after which it is washed with 20 cm of cyclohexane and dried at
five
0
five
peridyl) - -oxy-1,8-naphthyridine, melted at 174 C.
Example 47. They act in the same way as in Example 1, however, 13.3 g of 4-ethoxybenzoic acid, 12.9 g of N, N -carbonyldiimidazole and g of 2-amine-7-chloro-1,8-naphthyridine are used as starting materials. The compound obtained by precipitation in water (15.3 g, mp approx.) Is dissolved in 500 cm of boiling acetonitrile. After cooling for 16 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed 3 times with 25 cm of acetonitrile and dried under reduced pressure (0.067 kPa).
8 g of P- (7-chloro-1,8-naphthyridine-2-1w) -A-ethoxybenzamide, melted at 208 ° C, are obtained.
Example 48, Acts as indicated in Example 1, but used as starting materials. use 8 g of 4-ethoxybenzoic acid, 7.8 g of N, N -carbonyldiimidazole
and 5.6 g of 2-amine-7-methoxy-1,8-naphthyri-10 dyne. The compound obtained by precipitation in water (9.4 g, mp. 74 s) is dissolved in 94 cm of boiling acetonitrile. After cooling for 3 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed three times with 20 cm of acetonitrile and dried at 30 ° C.
lendioxybenzamide, melting at 256 ° C.
Example 51. They act in the same way as in Example 1, however, 6.6 g of 3-dimethylaminbenzo- are used as starting compounds; hydrochloric acid, 6.5 g of N, N -carbonyldiimidazole and 5.4 g of 2-amine-7-chloro-1,8-naphthyridine. The compound obtained by precipitation in water 49 g, so pl. 212 C), dissolved in
PE
CM-V boiling point - 4 C, hard 15
at
under reduced pressure
400
go acetonitrile. After 3 times, which is carried out at the time of the crystallization, the substance is separated by filtration, washed three times with 20 cm of acetonitrile /, and dried in a and. reduced pressure (0.067 kPa). 6.2 g of N- (7- (0.067 kPa) are obtained. 7 g of N- (7-labels-20 OR 8-naphthyridin-2-yl) -3-dimethyl-; s-1.8-naphthyridine- 2-yl) -4-ethoxybenzamine benzamide, melted at. , amide, melted at 145 C.
Example 49. The procedure is the same as in Example 1, however, 15.5 g of 4-butoxybenzoic acid, 12.9 g of N, N -carbonyldiimidazole and 8.9 g of 2-amine-7-chloro are used as starting compounds. 1,8-naphthyridine .. Compound obtained by
thirty
deposition in
-.about
water (about 18 g, mp. 140 ° C) is purified by chromatography on a column having a diameter of 40 mm, containing 200 g of silica (0.063-0.2 mm), using methylene chloride as an eluant 3 to 60 cm. After dry concentration of fractions 8-12, carried out at 40 ° C and under reduced pressure (4 kPa), 6.2 g of N- (7-xnop-1,8-naphthyridin-2-yl) are obtained. -4-butoxybenzamide, melting; at 197 ° C.
Example 50. They act in the same way as in Example 1, but 16.6 are used as starting materials. g of 3,4-methylenedioxybenzoic acid, 16.2 g of N, N -carbonyldiimidazole and 11.7 g of 2-amine-7-chloro-1,8-naphthyridine. The compound obtained by precipitation in water (15.7 g, mp. 256 ° C) is dissolved in 1000 cm of 1-propanol. After cooling for 16 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed 3 times with 20 cm of 1-propanol and dried at 40 ° C and under reduced pressure (0.067 kPa). 8.4 g of N- (7-chloro-1,8-naphthyridin-2-yl) -3,4-methy Example 52. They act as indicated in Example 1, however, 18.6 g of 3-dimethylamine-benzoic acid, 17.8 g g N, N -carbonyldiimidazole and 12.3 g 2-amine-7-methoxy-1,8-naphthyridine. The compound obtained by olesion in water (24.7 g, t. 82-84 C) is purified by chromatography on a column having a diameter of 4.5 cm, containing 220 g of silica (0.040-0.063 mm), wire elution with a mixture of (98-2, .jg volume) dichloromethane and methanol,. The fractions are collected in an amount of 100 cm, while the fractions 7-22 are combined and concentrated at 40 ° C and under reduced pressure (4 kPa) to obtain 24 g of a solid melting at 90 ° C. This compound is dissolved in 120 see boiling acetonitrile. After cooling for 1 hour at 4 ° C, the solid that crystallized out was separated by filter 40.
45
Vani, washed twice with 10 cm of isopropyloxyl and dried at 40 ° C under reduced pressure (0.5 mm Hg). 5.7 g of K- (7-methoxy-1 y8-naph-.gQ tiridine-2- silt) -3-dimethyllaminebenzamide, melted at 130 ° C.,
Example 53. They act in the same way as in Example 1, however, 23.1 g of 3-dimethylbenzamide benzoic acid, 22.7 g of N, N -carbonyldiimidazole and 23.7 g of 2-amine-7-phenoxy-1 are used as starting materials, 8- naphthyridine. The compound obtained by precipitation in water (44 g, so pl.
55
lendioxybenzamide, melting at 256 ° C.
Example 51. Analo is valid. it is indicated in Example 1, however, 6.6 g of 3-dimethylamine benzoate is used as the starting compound; hydrochloric acid, 6.5 g of N, N -carbonyldiimidazole and 5.4 g of 2-amine-7-chloro-1,8-naphthyridine. The compound obtained by precipitation in water 49 g, so pl. 212 C), dissolved in
PE
CM-V boiling or cooling 4 C, hard5
400
go acetonitrile. After 3 times, which is carried out at the time of the crystallization, the substance is separated by filtration, washed three times with 20 cm of acetonitrile /, and dried in a and. reduced pressure (0.067 kPa). 6.2 g of N- (7-OR 8-naphthyridin-2-yl) -3-dimethyl-aminobenzamide, melted at.
Example 52. They act in the same way as in Example 1, however, 18.6 g of 3-dimethylaminobenzoic acid, 17.8 g of N, N -carbonyldiimidazole and 12.3 g of 2-amine-7-methoxy-1 are used as starting compounds. , 8-naphthyridine. The compound obtained by olesion in water (24.7 g, t. 82-84 C) is purified by chromatography on a column having a diameter of 4.5 cm, containing 220 g of silica (0.040-0.063 mm), wire elution with a mixture (98-2 by volume) of dichloromethane and methanol,. . The fractions are collected in an amount of 100 cm, while the fractions 7-22 are combined and concentrated at 40 ° C and under reduced pressure (4 kPa) to obtain 24 g of a solid melting at 90 ° C. This compound is dissolved in 120 see boiling acetonitrile. After cooling for 1 hour at 4 ° C, the solid that crystallized out was separated by filtration.
vanilla, washed twice with 10 cm of isopropyloxyl and dried at 40 ° C under reduced pressure (0.5 mm Hg), 5.7 g of K- (7-methoxy-1 y8-naphthyridin-2-yl) are obtained -3-dimethyllabenzamide, melted at 130 ° C.,
Example 53. They act in the same way as in Example 1, however, 23.1 g of 3-dimethylbenzamide benzoic acid, 22.7 g of N, N -carbonyldiimidazole and 23.7 g of 2-amine-7-phenoxy-1 are used as starting materials, 8- naphthyridine. The compound obtained by precipitation in water (44 g, so pl.
2914
approx.), dissolved in 1000 cm of boiling acetonitrile. After cooling for 3 hours, the solid that crystallized out was separated by filtration, washed three times with 50 cm of acetonitrile and dried under reduced pressure (0.067 kPa). 32 g of K- (7-fenoc si-1,8-naphthyridin-2-yl) -3-dimethyl-aminobenzamide, melting at 120 ° C. are obtained.
Example 54. They act in the same way as in Example 1, however, 3.7 g of nicotinic acid, 4.9 g of N, N -carbonyldiimidazole and 3.6 g of 2-amine-7-hpor-1,8-naphthyridine are used as starting compounds. . The compound precipitated from the mixture is separated by filtration, after which it is washed 3 times with 20 cm of tetrahydrofuran-a. 3 times 50 cm of water, and then dried at 50 s and under reduced pressure (0.067 kPa). The resulting compound (4.75 g, t.g.) par is stored in 435 cm of boiling acetonitrile. After cooling for 2 hours at 4 ° C, the solid which crystallized out was separated by filtration, after which it was washed 3 times with 20 cm of acetonitrile and dried at 50 ° C under reduced pressure (0.067 kPa). (7-chlorophor-1,8-naphthyridin-2 yl) -3-pyridylcarboxamide melting at 200 ° C. .
Example 55. They act in the same way as in Example 1, however, 7.4 g of nicotinic acid, 9.7 g of N, N -carbonyldiimidazole and 7 g of 2-amine-7-methoxy-1,8-naphthyridine are used as starting materials. After filtering, washing in water and drying, the solid, crystallized during the reaction (10.3 g, T.Sh1. 245 ° C), is dissolved in 900 cm of boiling 1-propanol. The solid that crystallized out after 3 hours cooling at 4 ° C was separated by filtration, washed three times with 20 cm of 1-propanol and dried under reduced pressure (0.067 kPa). 8.7 g of M- (7-methoxy-1,8-naphl - tiridin-2-yl) -3-pyridylcarboxamide, melted at 247 ° C.
Example 56. Acting as indicated in Example 1, however, 1.7 g of 6-methoxypyridine-3- are used as starting compounds. carboxylic acid, 1.8 g N, N -carbonyldiimidazole and 1.95 g 2-amine-7
7 30
chlorine-1,8-naphthyridine. The resulting compound (2.5 g, mp. 270 ° C) is dissolved in 190 cm3 of a mixture of dimethylformamide and methanol (1/6). After cooling for 1 hour at 4 ° C, the solid that crystallized was separated by filtration. washed twice with 10 cm of methanol and dried at 40 ° C under reduced pressure (0.066 kPa). 2.1 g of N- (7-chloro-1,8-naphthyridin-2-sh1) -6-methoxy-3-pyridine carboxamide, melting at 270 ° C, are obtained.
6-Methoxy-3-pyridinecarboxylic acid can be obtained as follows.
To suspension A, 15 g of 6-chloro-3-pyridinecarboxylic acid in 40 cm of methanol was added 40 cm of 4 M methanol solution of sodium methane. The mixture is heated to reflux for 60 hours. The solvent is distilled off under reduced pressure.
(4 kPa). The residue is dissolved in 100 cm of distilled water, and the mixture is acidified to pH 5 with the aid of an aqueous 11.9 M hydrochloric acid solution. The precipitate obtained is separated by filtration, then it is flashed 5 times with 10 cm.
distilled water and air dried. 3.3 g of 6-methoxy-3-pyridinecarboxylic acid are obtained, melting at 180 ° C.
Example 57. They act in the same way as in Example 1, however, 4.7 g of 6-methoxy-3-pyridine-carboxylic acid, 4.9 g of N, N-Kap-bonyldiimidazole and 9.1 g of 2-amine are used as starting compounds. -7-,
fvnoxy-1,8-naphthyridine. The compound obtained by precipitation in water (11 g, mp. 115 ° C) is dissolved in 50 cm of boiling acetonitrile. After cooling for 10 hours at 20 ° C, the solid that crystallized out was separated by filtration, then washed three times with 10 cm of diisopropyl ether and dried at 30 ° C under reduced pressure. (0.067 kPa).
7 g of K- (7-phenoxy-1, B-naphthyridine-2-yl) -6-methoxy-3-pyridinecarboxamide are obtained, melting at 115-120 C.
Example 58. They act similarly to that specified in Example 1, however, 9 g of 2-thiophenecarboxylic acid, 11.2 g of N, N -carbonyldiimidazole and 9.5 g of 2-amine-7-chloro-1.8 are used as starting compounds. nafti
31
readin Soya; The line obtained by precipitation in water (9.6 g, m.p., 242 ° C) is dissolved in 700 cm of boiling ethanol. After 1 hour cooling, carried out at 4 ° C, the solid that crystallized out was separated by fingulation, washed twice with 25 cm of ethanol and dried at 40 ° C under reduced pressure (0.067 kPa). 7.5 g of N- (7-chloro-1.8 -naphthyridin-2-yl) -2-thiophene-carboxamide, melted at 244 s.
Example 55. They act similarly to that indicated in gfimer 1, however, as starting compounds, 16 g of 3-thiophenecarboxylic acid, 20.1 g of N, N -carbonyldiimidazol and 16.8 g of 2-amine-7-chloro-1.8 -naphthyridine. The compound obtained by precipitation in water (10.6 g, mp. 250 ° C) is dissolved in 980 cm of boiling acetonitrile. After cooling for 2 hours at 4 ° C, the solid that crystallized out was separated by filtration, which was then washed twice with 25 cm of acetonitrile and dried at 40 seconds under reduced pressure (0.067 kPa). Obtain 7.5 g of N- (7-chloro-1,8-naphthyridin-2 yl) -3-tiofenc boxbamide, melting at 254 ° C.
Example. 60. They act in the same way as in Example 1, however, 14 g of 2-thiophenecarboxylic acid, 17.8 g of N, N -carbonyldiimidazole and 12.3 g of 2-amine-7-methoxy-1,8-naphthyne are used as starting compounds. readin The compound obtained by precipitating it with water (19.5 g, mp. Dissolves in 750 cm of boiling ethanol. After cooling for 3 hours, n) at the solid, the crystallized substance is separated by filtration, after which it is washed 2 25 cm of ethanol and dried at 40 ° C and under reduced pressure (0.067 kPa). 15.6 g of N- (7-methoxy-1,8-naphthyridin-2-yl) -2-thiophene-carboxamide are obtained, melting at 220 C.
Example 61. They operate under conditions similar to those specified in Example 1, however, 4 g of 2-thiophenecarboxylic acid, 5.1 g of N, N -carbonyldiimidazole and 7 g of 2-amine-7-chloro are used as starting materials. 1,8- naphthyridine. The compound obtained by precipitation in water (8.8 g, mp 175 ° C) is dissolved in 150 cm of boiling methanol. After 3 hours of cooling.







97
32
carried out at 4 (, the solid that crystallized out was separated by filtration, after which it was washed 3 times with 10 cm of methanol and dried at 40 ° C and under reduced pressure (0.067 kPa). 6 g of N- (7-phenoxy-1,8-naphthyridine -2-yl) -2-thio-phencarboxamide, melted at 176 C.
Example 62. They act in the same way as in Example 1, however, as starting compounds, 5 g of 3-thiophenecarboxylic acid, 6.3 g of N, N -carbonyldiimidazole and 8.3 g of 2-amine-7-phenoxy-1,8-naphty are used - Ridin. The compound obtained by precipitation in water (11.6 g, mp. 110 ° C) is dissolved in 50 cm of boiling acetonitrile. After. 2 hours of cooling at 4 ° C, the solid, precipitated substance is separated by filtration, after which it is washed 3 times with 10 cm of diisopropyl ether and dried at 35 ° C under reduced pressure (0.067 kPa). Obtain 8.2 g of N- (7-phenoxy-1,8-naphthyridin-2-yl) -3-thiofenccarboximide, melting at 95 ° C.
Example 63o: They act in the same way as in Example 1; however, 4.1 F 5-metsh-2-2-thiophenecarboxylic acid, 5.6 g of N, N-carboxy-di-imidazole and 4.85 g of 2-amine-7 are used as starting compounds. chlorine-1,8-naphthyridine. The compound, which was obtained (3.8 g, so pl., Was dissolved in 150 cm of boiling acetonitrile. After cooling for 4 hours,
at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed 2 times with 10 cm of acetonitrile and dried at 40 ° C under reduced pressure (0.066 kPa),
3.1 g of H- (7-chloro-1,8-naphthydidin-2-yl) -5-methyl-2-thiofencap6ococamidea are obtained by melting at 222 ° C.
Example 64. They act in the same manner as in Example 1, however, 8.95 g of 2-furancarboxylic acid are used as starting compounds. acids, 12.8 g of N, N -carbonyldiimidazole and 10.5 g of 2-a shn-7-methoxy-1,8-naphthyridine. The compound obtained by precipitation in water (15.5 g, mp. 199 ° C) is dissolved in 500 cm of boiling ethanol. After 2 hours of cooling, carried out at 4 ° C, the solid crystallized substance that has been sprinkled is separated by
filtration, followed by washing it with 1) T twice with 10 cm of ethanol and sushi, at at a reduced pressure (0.067 kPa) .. 13.5 g of N- (7-methoxy-1,8-naphthyridin-2-yl) - are obtained 2-furan carboxamide, melted at 201 ° C,
Example 65. They act in the same manner as in Example 1, but 7.5 g of 2-furancarboxylic acid is used as starting compounds. lots, 10.9 g of N, N -carboni-lidimidazol and 11.9 g of 2-amine-7-phenoxy-1,8-naphthyridine. The compound obtained by precipitation in water (15.7 g, mp. 164 ° C) is dissolved in 200 cm of boiling ethanol. After cooling for 2 hours at 4 ° C, the solid that crystallized out was separated by filtration, after which it was washed with 15 cm of ethanol and dried under reduced pressure (0.067 kPa). 14.4 g of N- (7-phenoxy-1,8-naphthyridin-2-yl) -2-furancarboxamide are obtained, melting at 167 ° C,
Example 66. They act in the same way as in the example 1, but 7.5 g of 3-furancarboxylic acid, 10.9 g of N, N -carbonyldiimnadazole and 11.9 g of 2-amine-7-phenoxy are used as starting compounds. 1.8 naphthyne shchna. The compound obtained by precipitating in water (13g, mp approx. 90 ° C) is dissolved in BO cm of boiling acetonitride. After cooling for 2 hours with the solid that crystallized out, separated by filtration, then it was washed 2. times with 10 cm of acetonitrile and dried under reduced pressure (0.067 kPa). 10.7 g of K- (7-phenoxy-1 , 8-naphthyridin-2-yl) -3-furancarboxamide, melted at.
Example 67. To a solution of 12 g of b-methylpyridazine-3-carboxylic acid in 250 cm of anhydrous tetrahydrofuran, 20 g of N, N -carbonyldiimidazole are added. Note slow gas emission. The mixture is stirred at, until the end of the gas. Then 11 g of 2-amine-7-chloro-1, 8-naphthyridine are added and the mixture is heated at reflux for 20 hours. The precipitate formed is separated by filtration, then it is washed in ethanol, dried in air, and then extracted with 1000 cm of isopropanol with reflux c. extractor solid-liquid. for 20 hours. After 2 hours cooling at 4c, the isopropanol solution obtained in this manner crystallizes out a solid, which is separated by filtration and then dissolved in 300 cm of warm dimethylformamide ().
After cooling for 3 hours at 4 ° C, the solid that crystallized out was separated by filtration, then washed twice with 20 cm of methanol and dried at 40 ° C and under reduced pressure (0.066 kPa). 4.5 g of N- (7-chloro-1,8-naphthyridin-2-yl) -b-methyl-3-pyridazine carboxamide are obtained, melting at 258 C.
PRI mepera 68. Acts as indicated in Example 8, however, 10.7 g of 2-amine-7-chloroquinoline in 120 cm of anhydrous pyridine and 15.5 g of benzoyl chloride are used as starting compounds. The compound obtained by precipitation in water (16 g, mp), in | slit T by filtration, after which it is dissolved in 1000 cm of boiling cyclohexane. After cooling for 5 h at 4 ° C, the solid that crystallized out was separated by filtration and dried at 45 ° C under reduced pressure. (0.067 kPa). 12,, 9 g of compound are obtained, melting at, which is again crystallized in 60 cm of boiling acetone. After cooling for 1 hour at 4. ° C, the solid crystallized substance is separated by filtration, washed twice with 5 cm of acetone and dried at 40 ° C under a reduced pressure (0.067 kPa). -.
 9 g of N- (7-chloro-2-xynol) are obtained - benzam, melted at.
Example 69. Operate under conditions of example 1, but. out of 14 g of 2-fluorobenzoic acid, 16,, 2 g of N, N -carbonyldiimidazole and 13.7 g of 2-amino-7-methoxy-naphthyridine-1.8.
The compound obtained by precipitation with water (22 g, m.p., 181 ° C) is dissolved in 350 cm of boiling acetonitrile. After cooling for 3 hours at 4 ° C, the solid crystallizes and is filtered off, washed, twice 15 cm of acetonitrile and dried at 45 ° C under reduced pressure (0.07 kPa). 20 g of N- (7-methoxy-1, 8-naphthyridin-2-1x) -2-fluorobenzamide, melted at, are obtained.
Example 70. Work in the same way, 1Uluchay-K- (7-hydroxymethyl-1,8-naphthyridin-2-yl) 4-methoxybenz-am1-schA, so pl. 218 ° C.
Example 71. In a similar manner, K- (7-chloro-1,8-naphthyridin-2-yl) -1,2,5,6-tetrahydro-1-pyridinecarbox-S amide, m.p. 173 ° C.
These products have been tested in bio4
logical tests.
The proposed compounds have particularly interesting pharmacological properties. They exhibit an anxiolytic action, a hypnotic effect, an anticonvulsant action, an antiepileptic effect and an obesity in the 7-position of the methoxy group or a phenoxy group, and also exhibit antiviral activity.
Antiviral activity appears to be clearly in vivo on influenza viruses A and B at concentrations of 1.5-30 pg / cm.
In addition, these compounds develop in vivo significant protective activity against influenza infection (A, jAm Arbor) of mice at doses of 30-300 mg / kg, orally.
The proposed compounds have a low toxicity: their LDjo is parorally for the younger one is 300-900 mg / kg and the doses exceed 900 mg / kg.
Data on the affinity of the compounds obtained for 1, the central areas of the benolay relaxing the muscular system 20 Diazepines and toxicity are given
by a good level, what about in-table. one.
The test is described below. Ana closest structural anaimno they have good means
in vitro to benzodi receptor sites
The log of compounds obtained is a compound of the formula
Averaging at a concentration of from 5 to values close to 1000 pM, according to a known technique.
In animals (microorganisms), these compounds manifest their effect at doses.
25
CHjCONH-Y Y V
Activity data of this compound
equal to 10-200 mg / kg, orally, at ot-zo and pentatrazole are summarized in table. 2
It follows from the comparison that the products offered are superior to the activity of known compounds.
against seizures caused by pentatrazole, in accordance with the known method.
Immunostimulatory activity appears in vitro at molar concentrations equal when stimulating the cytostatic activity of the peritoneal macrophages in mice against tumor cells in accordance with the known method appears in vivo in micehay — they stimulate protective reactions against infection at a dose equal to 2-20 mg / kg intraperitoneally, according to a known method.
The advantage of the immunostimulating effect of the compounds is their use as an anti-infective agent, which has the ability to counteract microbes that have become resistant to traditional antibiotics.
In addition, the compounds according to the invention, wherein R is 4-methoxyphenyl, 3-thienyl or 5-methylthienyl, and Het is 1,8-naphthyridin-2-yl, substituted at the 7 position of chlorine atoms, with a methoxy group or oxymethyl, or -. e where R -2-.thiensh1, and Het - 1,8-naphthyridin-2-yl, substituted
7 at the position of a methoxy group or a phenoxy group, also exhibit antiviral activity.
Antiviral activity appears to be clearly in vivo on influenza viruses A and B at concentrations of 1.5-30 pg / cm.
In addition, these compounds develop in vivo significant protective activity against influenza infection (A, jAm Arbor) of mice at doses of 30-300 mg / kg, orally.
The proposed compounds have a low toxicity: their LDjo is parorally for the younger one is 300-900 mg / kg and the doses exceed 900 mg / kg.
The data on the affinity of the compounds obtained for 1, the central sites by the bioengineer of the compounds is the compound of the formula
25
CHjCONH-Y Y V
Activity data of this compound
35
up to g
It follows from the comparison that the proposed products translate into the activity of the known compounds.

权利要求:
Claims (1)
[1]
Invention Formula
The method of obtaining the substituted amide derivative of the general formula
R - CONH - Het
(I)
de R is phenyl or phenyl substituted by lower alkyl, 1 or 2 fluorine atoms or hydroxy group, or substituted in position 3 or 4 by alkyloxy group, methylenedioxy group or substituted in position 3 by dialkylamine, or
R is a heterocycle selected from 3-pyri. Esil, 3-alkyloxypyridyl, thienyl, alkylthienyl, furyl, alkyl pyridazine; or tetrahydropyridyl; Het is 2-quinolyl substituted at the 7 position with a halogen, or 1,8-naphthyridin-2-yl, not substituted or substituted at the 7 position with a halogen, alkyl 37
1A G / 797
scrap, annloxy group, an alkylnoxoxyloxy group, an alkoxyloxy group, or an alkynyloxy group containing 3 or 4 carbon atoms, an apythio group, a benzylthio group, a phenoxy group, not substituted or substituted by fluorine, chlorine or bromine, 10 in a position 2, or a substitute, or a substitute for a non-substituted, fluorine, chlorine or bromine group in a position 2, or a substitute , 1 or 2 methyl atoms, or a pyridyloxy group, or an alkyl piperidyloxy group, with -jg this, when Het is 2-quinoyl, then R is not phenyl,
alkyls and alkyl parts have or branched structure and t 1-4 carbon atoms, about t - 20
Data on the activity of the compounds obtained and their toxicity
82
38
that acid
and y and u with the formula
R - COOH
where R has the indicated meanings; in the presence of a peptide condensation agent, such as N, N -carbonyldiimidazole, its reactive derivative in the presence of an acid acceptor such as a nitrogen-containing base, is reacted with an amine of the general formula
 - het
where Het has the indicated values, with the introduction of protection of the hydroxy groups in the starting compounds, after which, if necessary, the protective groups are removed and the resulting product is isolated
Table 1
37.5
17.5 16.7 17.5
66
36.5
87.5
25
24.4
200
50
44
116
60
eleven
20
nineteen
Nontoxic 900
900
Non-toxic 900 900
Nontoxic 900 nontoxic 900
900 non-toxic 900
eleven
eleven
900 900 900 900 900 900 900 900
41
1417797, 42
Continuation of table 1

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同族专利:

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公开号 | 公开日

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FI79313C|1989-12-11|

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DK327285A|1986-01-20|

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HUT40799A|1987-02-27|

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HU199802B|1990-03-28|

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EP0172083B1|1988-04-20|

---

IL75817A|1988-06-30|

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PL254570A1|1986-10-21|

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EP0172083A1|1986-02-19|

---

CA1224787A|1987-07-28|

---

PT80840B|1988-02-17|

---

ES545336A0|1986-02-01|

---

AT33652T|1988-05-15|

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YU118785A|1988-10-31|

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FI852821A0|1985-07-18|

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IL75817D0|1985-11-29|

---

PH21301A|1987-09-28|

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US4642308A|1987-02-10|

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NO161673B|1989-06-05|

---

DD240011A5|1986-10-15|

---

PL145331B1|1988-09-30|

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AU4509085A|1986-01-23|

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NO161673C|1989-09-13|

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KR860001100A|1986-02-22|

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PT80840A|1985-08-01|

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ES8604584A1|1986-02-01|

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MA20487A1|1986-04-01|

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JPS6163656A|1986-04-01|

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NO852877L|1986-01-20|

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ZA855409B|1986-04-30|

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DK327285D0|1985-07-18|

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NZ212764A|1988-05-30|

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AU572672B2|1988-05-12|

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FR2567887B1|1986-12-19|

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FI79313B|1989-08-31|

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DE3562250D1|1988-05-26|

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FI852821L|1986-01-20|

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OA08069A|1987-03-31|

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CS253730B2|1987-12-17|

---

FR2567887A1|1986-01-24|

---

GR851774B|1985-11-26|

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BRPI0606365A2|2005-02-28|2017-06-27|Renovis Inc|compound or a pharmaceutically acceptable salt, solvate or prodrug thereof and stereoisomers and tautomers thereof, pharmaceutical composition, methods for preventing, treating, ameliorating or controlling a disease or condition and for preparing a compound, use of a compound or a salt , solvate or pharmaceutically acceptable composition thereof, method of treating a mammal, and, combination|

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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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FR8411442A|FR2567887B1|1984-07-19|1984-07-19|NEW SUBSTITUTED AMIDES, THEIR PREPARATION AND THE MEDICINAL PRODUCTS CONTAINING THEM|

---