IP Library Granted Patent US 7,652,058
Granted Patent B2
US 7,652,058 · App. 11/792,514 · Granted Jan 26, 2010

Octahydropyrano[3,4-C]pyrrole tachykinin receptor antagonists

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Quick Facts
Patent No.
US 7,652,058
App. No.
11/792,514
Granted
Jan 26, 2010
Kind
B2
Abstract

The present invention is directed to certain hydropyranopyrrolidine compounds which are useful as neurokinin-1 (NK-1) receptor antagonists, and inhibitors of tachykinin and in particular substance P. The invention is also concerned with pharmaceutical formations comprising these compounds as active ingredients and the use of the compounds and their formulations in the treatment of certain disorders, including emesis, urinary incontinence, depression, and anxiety.

Claims (78)

1. A compound of the formula I:

wherein:

R 1 is selected from the group consisting of:

(1) hydrogen,

(2) C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl,

(3) cyclopentenone, which is unsubstituted or substituted with hydroxyl or methyl,

(4) furanone, which is unsubstituted or substituted with methyl,

(5) —(CO)—C 1-6 alkyl,

(6) —(CO)—NH 2 ,

(7) —(CO)—NHC 1-6 alkyl, and

(8) —(CO)—N(C 1-6 alkyl)(C 1-6 alkyl);

X, Y and Z are independently selected from the group consisting of:

(1) hydrogen,

(2) halo, and

(3) methyl;

and pharmaceutically acceptable salts thereof and individual enantiomers and diastereomers thereof.

2. The compound of claim 1 of the formula Ia:

and pharmaceutically acceptable salts thereof and individual enantiomers and diastereomers thereof.

3. The compound of claim 1 of the formula Ib:

and pharmaceutically acceptable salts thereof and individual enantiomers and diastereomers thereof.

4. The compound of claim 1 wherein R 1 is selected from the group consisting of:

(1) hydrogen,

(2) C 1-3 alkyl, which is unsubstituted or substituted with hydroxyl or phenyl,

(3) cyclopent-2-en-1-one, which is unsubstituted or substituted with hydroxyl or methyl,

(4) furanone, which is unsubstituted or substituted with methyl,

(5) —(CO)—C 1-3 alkyl,

(6) —(CO)—NH 2 ,

(7) —(CO)—NHC 1-3 alkyl, and

(8) —(CO)—N(C 1-3 alkyl)(C 1-3 alkyl).

5. The compound of claim 1 wherein R 1 is selected from the group consisting of:

(1) hydrogen,

(2) methyl,

(3) 2-phenylethyl,

(4) 2-hydroxyethyl,

(5) cyclopent-2-en-1-one,

(6) 5-hydroxycyclopent-2-en-1-one,

(7) 4-hydroxycyclopent-2-en-1-one,

(8) 2-methylcyclopent-2-en-1-one,

(9) 5-furanone,

(10) acetyl,

(11) acetamido,

(12) methyl-acetamido, and

(13) dimethyl-acetamido.

6. The compound of claim 1 wherein X is fluorine, Y is hydrogen, and Z is hydrogen.

7. The compound of claim 1 wherein X is methyl, Y is hydrogen, and Z is hydrogen.

8. A compound which is selected from the group consisting of:

9. A compound of claim 1 selected from the group consisting of

and pharmaceutically acceptable salts thereof,

10. A compound of claim 1 of the formula

Ex

R 1

X

28

4-F

29

4-F.

11. A compound of claim 1 of the formula

Ex. #

R 1

X

30

4-F

31

Me

4-F

32

H

33

4-F

34

2-Me

35

2-Me

36

2-Me

37

4-F.

12. A pharmaceutical composition which comprises an inert carrier and a compound of claim 1 or a pharmaceutically acceptable salt thereof.

Assignments (2)
CHANGE OF NAME Recorded Nov 24, 2009
From: MERCK & CO., INC
To: MERCK SHARP & DOHME CORP.
Reel/Frame 023563/0437 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2007
From: DEVITA, ROBERT J; JIANG, JINLONG; MILLS, SANDER G; YOUNG, JONATHAN R.
To: MERCK & CO., INC
Reel/Frame 019959/0886 →