IP Library Granted Patent US 7,879,848
Granted Patent B2
US 7,879,848 · App. 11/910,370 · Granted Feb 1, 2011

Dipeptidyl Peptidase-IV inhibiting compounds, method of preparing the same, and pharmaceutical compositions containing the same as an active agent

Assignee: LG Life Sciences, Ltd.
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Quick Facts
Patent No.
US 7,879,848
App. No.
11/910,370
Granted
Feb 1, 2011
Kind
B2
Abstract

Novel compounds exhibiting good inhibitory activity versus Dipeptidyl Peptidase-IV(DPP-IV) include those of the following formula (1) or pharmaceutically acceptable salt thereof: wherein A is a substituted or unsubstituted 1,4,5,7-tetrahydro-pyrazolo[3,4-c]pyridine, 5,6 -dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazine, 4,5-dihydro-7H-isooxazolo[3,4-c]pyridine, 3,4 -dihydroisoquinoline, 5,8-dihydropyrido[3,4-d]pyrimidine, or 6,7 -dihydro[1,3]thiazolo[4,5,c]pyridine, and B is a substituted or unsubstituted piperidin-2-one, morpholin-3-one, oxazolidin-2-one, pyrrolidin-2-one, or 1,5-dihydro-pyrrol-2-one. Methods of preparing the novel inhibitory compounds of formula (1) and pharmaceutical compositions containing the same as an active agent are disclosed.

Claims (110)

1. A compound of the following formula (1) or pharmaceutically acceptable salt thereof:

wherein

A is a substituent of the following formula (5):

wherein R 3 is hydrogen, or substituted or unsubstituted C 1 -C 4 alkyl, cycloalkyl, aryl or heteroaryl; and R′ 3 is hydrogen, or CF 3 ;

B is selected from the group consisting of substituents of the following formulas (8) to (11):

wherein R 7 , R 8 , R 9 and R 10 are each independently hydrogen, halogen, or substituted or unsubstituted C 1 -C 4 alkyl;

wherein R 11 , R 12 and R 13 are each independently hydrogen, halogen, or substituted or unsubstituted C 1 -C 4 alkyl; and Y is oxygen, sulfur or SO 2;

wherein R 14 and R 15 are each independently hydrogen, halogen, or substituted or unsubstituted C 1 -C 4 alkyl; and Z is —CH— or oxygen, where Z is oxygen, R 14 is nothing; and

wherein R 17 is substituted or unsubstituted C 1 -C 4 alkyl, wherein the substituted C 1 -C 4 alkyl is substituted with halogen.

2. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the halogen is fluoride.

3. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein R 3 is selected from the group consisting of:

hydrogen;

substituted or unsubstituted C 1 -C 4 alkyl;

formula —CH 2 -R 18 , wherein R 18 is C 1 -C 4 alkoxyalkyl, or C 3 -C 7 cycloalkyl unsubstituted or substituted with halogen or hydroxy, or phenyl unsubstituted or substituted with halogen or hydroxy, or heteroaryl;

substituted or unsubstituted C 3 -C 7 cycloalkyl;

formula

wherein R 19 and R 20 are each independently hydrogen, halogen, or substituted or unsubstituted C 1 -C 4 alkyl; and

5-membered or 6-membered heteroaryl unsubstituted or substituted with halogen or hydroxy,

wherein the substituted C 3 -C 7 cycloalkyl and C 1 -C 4 alkyl are the cycloalkyl and alkyl substituted with halogen or hydroxy.

4. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the heteroaryl is a 2-furan, 3-furan, 2-thiophene, 3-thiophene, 2-pyridine, 3-pyridine, 4-pyridine, 2-pyrrole or 3-pyrrole, unsubstituted or substituted with a halogen or hydroxy.

5. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound is a stereoisomer as represented in the following formula (1a):

wherein A and B are the same as in formula (1).

6. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of:

1-[2S-amino-4-oxo-4-(4-trifluoromethyl-5,8-dihydro-6H-pyrido[3,4-d]pyrimidin-7-yl)-butyl]-5R-methyl-1-piperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-phenyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-oxo-4-[2-phenyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-6-methylmorpholin-3-one;.

1-{(2S)-2-amino-4-oxo-4-[2-phenyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

1-{(2S)-2-amino-4-[2-cyclopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

1-{(2S)-2-amino-4-[2-cyclopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-cyclopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

1-{(2S)-2-amino-4-[2-(4-fluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-(4-fluorophenyl)-4-(trifluoromethyl)-5,8- dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-2-one;

1-{(2S)-2-amino-4-[2-(3-fluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4- d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-(3-fluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

(5R)-1-{(2S)-2-amino-4-[2-(4-fluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(3,4-difluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-(3,4-difluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

(5R)-1-{(2S)-2-amino-4-[2-(3,4-difluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-cyclopentyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-cyclopentyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

1-{(2S)-2-amino-4-[2-cyclopentyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-(2-methoxyethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(2-methoxyethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-(cyclopropylmethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(cyclopropylmethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-pyridin-4-yl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-oxo-4-[2-pyridin-4-yl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-(4-fluorobenzyl)-4-(trifluoromethyl)-5,8- dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(4-fluorobenzyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-(3-thienyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-oxo-4-[2-(3-thienyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-(2-thienyl)-4-(trifluoromethyl)-5,8- dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-oxo-4-[2-(2-thienyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-(2-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(2-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-(3-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(3-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-(1H-pyrrol-2-yl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-oxo-4-[2-(1H-pyrrol-2-yl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-pyridin-3-yl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-oxo-4-[2-pyridin-3-yl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

1-{(2S)-2-amino-4-[2-ethyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-ethyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

1-{(2S)-2-amino-4-[2-isopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

1-{(2S)-2-amino-4-[2-isopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-isopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

(5S)-1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-methyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin- 7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin- 7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

1-{(2S)-2-amino-4-[2-methyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin- 7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-[2-methyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one;

1-{(2S)-2-amino-4-oxo-4-[4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin- 7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-oxo-4-[4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-6-methylmorpholin-3-one;

4-{(2S)-2-amino-4-[2.4-bis(trifluoromethyl)-5,8- dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylthiomorpholin-3-one;

(5R)-1-{(2S)-2-amino-4-[2-ethyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-(pentafluoroethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

(6S)-4-{(2S)-2-amino-4-oxo-4-[2-(pentafluoroethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-6-methylmorpholin-3-one;

1-{(2S)-2-amino-4-oxo-4-[2-(pentafluoroethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-oxo-4-[2-propyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-oxo-4-[2-propyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-(fluoromethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one;

1-{(2S)-2-amino-4-[2-(fluoromethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one;

1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-methyl-1,5-dihydro-2H-pyrrol-2-one;

1-{(2S)-2-amino-4-[2-(3-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-methyl-1,5-dihydro-2H-pyrrol-2-one;

1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-methyloxopyrolidin-2-one;

1-{(2S)-2-amino-4-[2-(3-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-methylpyrolidin-2-one;

1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-(trifluoromethyl)piperidin-2-one;

1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-(trifluoromethyl)pyrolidin-2-one;

1-{(2S)-2-amino-4-[2-(3-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-(trifluoromethyl)pyrolidin-2-one;

1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-methyloxopiperidin-2-one;

1-{(2S)-2-amino-4-[2-(3-furyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-4-methylpiperidin-2-one;

(5R)-1-{(2S)-2-amino-4-[2-cyclobutyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one; and

1-{(2S)-2-amino-4-[2-cyclobutyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one .

7. A pharmaceutical composition for inhibiting Dipeptidyl Peptidase-IV(DPP-IV) comprising the compound according to claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.

8. The pharmaceutical composition according to claim 7 , wherein the composition is used for treating diabetes mellitus or obesity.

9. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (5R)-1-{(2S)-2-amino-4-[2-methyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

10. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (5R)-1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

11. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of 1-{(2S)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

12. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of 1-{(2S)-2-amino-4-[2-methyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

13. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (6S)-4-{(2S)-2-amino-4-[2-methyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

14. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (6S)-4-{(2S)-2-amino-4-[2-(4-fluorophenyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

15. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of 1-{(2S)-2-amino-4-[2-t-butyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

16. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (6S)-4-{(2S)-2-amino-4-[2-t-butyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

17. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (6S)-4-{(2S)-2-amino-4-[2-cyclopropyl-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-6-methylmorpholin-3-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

18. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (5R)-1-{(2S)-2-amino-4-oxo-4-[2-(pentafluoroethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5-methylpiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

19. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (6S)-4-{(2S)-2-amino-4-oxo-4-[2-(pentafluoroethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-6-methylmorpholin-3-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

20. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of 1-{(2S)-2-amino-4-oxo-4-[2-(pentafluoroethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]butyl}-5,5-difluoropiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

21. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of (5R)-1-{(2S)-2-amino-4-[2-(fluoromethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5-methylpiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

22. The compound according to claim 1 , or pharmaceutically acceptable salt thereof, wherein the compound or pharmaceutically acceptable salt is selected from the group consisting of 1-{(2S)-2-amino-4-[2-(fluoromethyl)-4-(trifluoromethyl)-5,8-dihydropyrido[3,4-d]pyrimidin-7(6H)-yl]-4-oxobutyl}-5,5-difluoropiperidin-2-one, and salts thereof with maleic acid, phosphoric acid, tartaric acid, hydrochloric acid, methanesulfonic acid or citric acid.

Assignments (3)
MERGER Recorded Sep 2, 2017
From: LG LIFE SCIENCES LTD.
To: LG CHEM, LTD.
Reel/Frame 043475/0619 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 019903 FRAME 0916. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNEE ADDRESS IS LG TWIN TOWER, 20, YOIDO-DONG, YOUNGDUNGPO-GU, SEOUL, 150-721. Recorded Aug 13, 2008
From: LEE, CHANG-SEOK; KOH, JONG SUNG; KOO, KI DONG; KIM, GEUN TAE; KIM, KYOUNG-HEE; HONG, SANG YONG; KIM, SUNGSUB; KIM, MIN-JUNG; YIM, HYEON JOO; LIM, DONGCHUL; KIM, HYE JIN; HAN, HEE OON; BU, SEONG CHEOL; KWON, OH HWAN; KIM, SUNG HO; HUR, GWONG-CHEUNG; KIM, JI YOUNG; YEOM, ZI-HO; YEO, DONG-JUN
To: LG LIFE SCIENCES, LTD.
Reel/Frame 021382/0626 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2007
From: LEE, CHANG-SEOK; KOH, JONG SUNG; KOO, KI DONG; KIM, GEUN TAE; KIM, KYOUNG-HEE; HONG, SANG YONG; KIM, SUNGSUB; KIM, MIN-JUNG; YIM, HYEON JOO; LIM, DONGCHUL; KIM, HYE JIN; HAN, HEE OON; BU, SEONG CHEOL; KWON, OH HWAN; KIM, SUNG HO; HUR, GWONG-CHEUNG; KIM, JI YOUNG; YEOM, ZI-HO; YEO, DONG-JUN
To: LG LIFE SCIENCES, LTD.
Reel/Frame 019903/0916 →
Priority Claims (4)
KR 10-2005-0027756 · Apr 1, 2005 · national
KR 10-2005-0053761 · Jun 22, 2005 · national
KR 10-2005-0085980 · Sep 15, 2005 · national
KR 10-2005-0122361 · Dec 13, 2005 · national
Continuity (1)
Related Publication 20080188471A1 · Aug 7, 2008