IP Library Granted Patent US 7,199,150
Granted Patent B2
US 7,199,150 · App. 10/889,657 · Granted Apr 3, 2007

Amino alcohol compounds

Assignee: Sankyo Company, Limited
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Quick Facts
Patent No.
US 7,199,150
App. No.
10/889,657
Granted
Apr 3, 2007
Kind
B2
Abstract

Amino alcohol compounds and phosphonic acid compounds having excellent immunosuppressive activity, pharmacologically acceptable salts thereof and pharmacologically acceptable esters thereof, and pharmaceutical compositions comprising such compounds, the compounds having the following formula: wherein R 1 and R 2 each represent hydrogen, or a protecting group of the amino group; R 3 represents hydrogen, or a protecting group of the hydroxyl group; R 4 represents a lower alkyl group; n is 1 to 6; X represents oxygen or nitrogen, which is unsubstituted or substituted with a lower alkyl group; Y represents ethylene; Z represents a C 1 –C 10 alkylene; R 5 represents an aryl group; and R 6 and R 7 each represents hydrogen; provided that when R 5 represents hydrogen, then Z represents a group other than a single bond or a straight chain C 1 –C 10 alkylene group.

Claims (53)

1. A compound of formula (Ia)

wherein R 1 and R 2 are each a hydrogen atom;

R 3 is a hydrogen atom;

R 4 is a C 1 –C 2 alkyl group;

n is 2;

X is ═N—D, wherein D is a hydrogen atom, a C 1 –C 4 alkyl group or a phenyl group;

Y is an ethylene group, an ethynylene group, a group of a formula —CO—CH 2 or a phenylene group;

Z is an ethylene group or a trimethylene group;

R 5 is an unsubstituted C 3 –C 10 cycloalkyl group, an unsubstituted C 6 –C 10 aryl group, or a C 3 –C 10 cycloalkyl group or a C 6 –C 10 aryl group substituted with from 1 to 3 substituents selected from the group consisting of a halogen atom, a lower alkyl group, a halogeno lower alkyl group and a lower alkoxy group;

R 6 and R 7 are each a hydrogen atom;

a pharmacologically acceptable salt thereof, or a pharmacologically acceptable ester thereof.

2. The compound according to claim 1 or a pharmacologically acceptable salt thereof, wherein R 4 is a methyl group.

3. The compound according to claim 2 or a pharmacologically acceptable salt thereof, wherein X is a group of a formula ═N—CH 3 .

4. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(3,4-dimethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol, or a pharmacologically acceptable salt thereof.

5. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(3,5-dimethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol, or a pharmacologically acceptable salt thereof.

6. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(3-trifluoromethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol, or a pharmacologically acceptable salt thereof.

7. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(4-trifluoromethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol.

8. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(4-methylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol.

9. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(4-methoxyphenyl)butanoyl]pyrrol-2-yl}butan-1-ol.

10. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(3-methylphenyl)butyl]pyrrol-2-yl}butan-1-ol.

11. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(3,4-dimethylphenyl)butyl]pyrrol-2-yl}butan-1-ol.

12. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1-methyl-5-[4-(3,5-dimethylphenyl)butyl]pyrrol-2-yl}butan-1-ol.

13. The compound according to claim 1 , wherein said compound is 2-amino-2-methyl-4-{1methyl-5-[4-(3-triflouromethylphenyl)butyl]pyrrol-2-yl}butan-1-ol.

14. The compound according to claim 1 , wherein R 1 , R 2 and R 3 are each a hydrogen atom, R 4 is a methyl group, n is 2 and Y—Z—R 5 is —(O—(CH 2 ) 3 -(4-F-phenyl).

15. The compound according to claim 1 , wherein the compound is selected from the group consisting of

2-amino-2-methyl-4-{1-methyl-5-[4-(3,4-dimethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(3,5-dimethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(3-trifluoromethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(4-trifluoromethylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(4-methylphenyl)butanoyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(4-methoxyphenyl)butanoyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(3-methylphenyl)butyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(3,4-dimethylphenyl)butyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(3,5-dimethylphenyl)butyl]pyrrol-2-yl}butan-1-ol;

2-amino-2-methyl-4-{1-methyl-5-[4-(3-triflouromethylphenyl)butyl]pyrrol-2-yl}butan-1-ol; and

a compound of the formula (Ia), wherein R 1 , R 2 and R 3 are each a hydrogen atom, R 4 is a methyl group, n is 2 and Y—Z—R 5 is —CO—(CH 2 ) 3 -(4-F-phenyl),

or a pharmacologically acceptable salt thereof.

16. The compound according to claim 4 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

17. The compound according to claim 5 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

18. The compound according to claim 6 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

19. The compound according to claim 7 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

20. The compound according to claim 8 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

21. The compound according to claim 9 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

22. The compound according to claim 10 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

23. The compound according to claim 11 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

24. The compound according to claim 12 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

25. The compound according to claim 13 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

26. The compound according to claim 14 , wherein the configuration at the carbon atom to which the group of the formula —NR 1 R 2 attaches is the R configuration, or a pharmacologically acceptable salt thereof.

27. A pharmaceutical composition comprising as an active ingredient a compound, a pharmacologically acceptable salt thereof or a pharmacologically acceptable ester thereof according to any one of claims 1 to 26 , in combination with a pharmacologically acceptable carrier.

28. A method for the treatment of a disease selected from the group consisting of rheumatoid arthritis and psoriasis in a human in need thereof, which comprises administering to said human a pharmaceutically effective amount of a compound, a pharmacologically acceptable salt or a pharmacologically acceptable ester according to any one of claims 1 to 26 .

29. The method according to claim 28 , wherein the disease is rheumatoid arthritis.

30. The method according to claim 28 , wherein the disease is psoriasis.

31. A method for the treatment of a disease selected from the group consisting of rheumatoid arthritis and psoriasis in a mammal in need thereof comprising administering to said mammal a pharmaceutically effective amount of a compound according to any one of claims 1 to 26 , a pharmacologically acceptable salt thereof or a pharmacologically acceptable ester thereof.

Assignments (2)
MERGER Recorded Aug 10, 2011
From: SANKYO COMPANY, LIMITED
To: DAIICHI SANKYO COMPANY, LIMITED
Reel/Frame 026724/0805 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2004
From: NISHI, TAKAHIDE; SHIMOZATO, TAKAICHI; NARA, FUTOSHI; MIYAZAKI, SHOJIRO
To: SANKYO COMPANY, LIMITED
Reel/Frame 015262/0154 →
Priority Claims (2)
JP 2002-004456 · Jan 11, 2002 · national
JP 2002-004484 · Jan 11, 2002 · national
Continuity (2)
Continuation In Part PCTJP030013600 · Jan 9, 2003
Related Publication 20050043386A1 · Feb 24, 2005