IP Library Granted Patent US 6,992,193
Granted Patent B2
US 6,992,193 · App. 10/458,135 · Granted Jan 31, 2006

Sulfonylamino phenylacetamide derivatives and methods of their use

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Quick Facts
Patent No.
US 6,992,193
App. No.
10/458,135
Granted
Jan 31, 2006
Kind
B2
Abstract

Sulfonylamino phenylacetamide derivatives of the general formula are disclosed. Pharmaceutical compositions containing the compounds and methods for their use are also disclosed. In certain embodiments, the compounds of the invention that, preferably: (1) bind with high affinity to κ opioid receptors; (2) display good opioid receptor selectivity of κ versus μ and κ versus δ; and (3) do not substantially inhibit cytochrome P450 enzymatic activity, in particular CYP2D6, CYP2C9 and CYP3A4.

Claims (34)

1. A compound of Formula I:

or a stereoisomer, prodrug, pharmaceutically acceptable salt, hydrate, solvate, acid salt hydrate, N-oxide or isomorphic crystalline form thereof;

wherein, independently:

n is an integer from 0 to 4;

R 1 is H or —OH;

R 2 is an optionally substituted alkyl or optionally substituted aryl;

R 3 is H, optionally substituted alkyl, or, when taken together with R 2 , forms an optionally substituted 4-7 membered heterocycloalkyl ring;

R 4 is H or optionally substituted alkyl;

R 5 is optionally substituted alkyl, optionally substituted aryl or optionally substituted heteroaryl; and

R 6 and R 7 are H; with the proviso that when n is 0, R 1 is hydrogen, R 3 is methyl, R 4 is hydrogen and R 5 is methyl or unsubstituted phenyl, then R 2 is other than unsubstituted phenyl, methoxyphenyl, hydroxyphenyl or methanesulfonylaminophenyl, and when n is 0, R 1 is hydroxy, R 3 is methyl, R 4 is hydrogen and R 5 is methyl, then R 2 is other than unsubstituted phenyl or trifluoromethylphenyl.

2. A compound according to claim 1 , wherein n is 1.

3. A compound according to claim 1 , wherein R 1 is H.

4. A compound according to claim 1 , wherein R 1 is —OH.

5. A compound according to claim 1 , wherein R 2 is optionally substituted alkyl.

6. A compound according to claim 5 , wherein R 2 is isopropyl.

7. A compound according to claim 1 , wherein R 2 is optionally substituted aryl.

8. A compound according to claim 7 , wherein R 2 is phenyl.

9. A compound according to claim 1 , wherein R 3 is H or optionally substituted alkyl.

10. A compound according to claim 9 , wherein R 3 is methyl.

11. A compound according to claim 1 , wherein R 2 and R 3 form an optionally substituted 4- to 7-membered heterocycloalkyl ring.

12. A compound according to claim 1 , wherein R 4 is H or lower alkyl.

13. A compound according to claim 12 , wherein R 4 is H or methyl.

14. A compound according to claim 1 , wherein R 5 is optionally substituted alkyl.

15. A compound according to claim 1 of Formula II:

16. A compound according to claim 1 of Formula III:

17. A compound according to claim 1 , wherein said compound is 2-[4-(methanesulfonylamino-methyl)-phenyl]-N-methyl-N-[1-(S)-phenyl-2-pyrrolidin-1-ylethyl]-acetamide.

18. A compound according to claim 1 , wherein said compound is N-{2-[3-(S)-hydroxy-pyrrolidin-1-yl]-1-(S)-phenyl-ethyl}-2-[4-(methanesulfonylamino-methyl)-phenyl]-N-methyl-acetamide.

19. A pharmaceutical composition, comprising:

a pharmaceutically acceptable carrier; and

an effective amount of a compound according to claim 1 .

20. A pharmaceutical composition according to claim 19 , further comprising an effective amount of at least one opioid.

21. A pharmaceutical composition according to claim 20 , wherein said opioid is selected from the group consisting of alfentanil, buprenorphine, butorphanol, codeine, dezocine, dihydrocodeine, fentanyl, hydrocodone, hydromorphone, levorphanol, meperidine (pethidine), methadone, morphine, nalbuphine, oxycodone, oxymorphone, pentazocine, propiram, propoxyphene, sufentanil, tramadol and mixtures thereof.

22. A pharmaceutical composition according to claim 19 , further comprising an effective amount of a compound selected from the group consisting of antibiotics, antivirals, antifungals, anti-inflammatories, anesthetics and mixtures thereof.

23. A compound according to claim 16 , wherein said compound is N-[4-(2-{2-[3-(S)-hydroxy-pyrrolidin-1-ylmethyl]-(S)-piperidin-1-yl}-2-oxo-ethyl)benzyl]methanesulfonamide.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jul 24, 2015
From: ROYAL BANK OF CANADA, AS ADMINISTRATIVE AGENT
To: CALIXA THERAPEUTICS, INC.; ADOLOR CORPORATION; CUBIST PHARMACEUTICALS, INC.
Reel/Frame 036180/0070 →
SECURITY AGREEMENT Recorded Nov 20, 2012
From: CUBIST PHARMACEUTICALS, INC.; ADOLOR CORPORATION; CALIXA THERAPEUTICS, INC.; CUBIST PHARMACEUTICALS HOLDINGS, INC.; CUBIST PHARMACEUTICALS U.S.
To: ROYAL BANK OF CANADA, AS ADMINISTRATIVE AGENT
Reel/Frame 029339/0669 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2003
From: BOURDONNEC, BERTRAND LE; AJELLO, CHRISTOPHER WILLIAM; DOLLE, ROLAND E.
To: ADOLOR CORPORATION
Reel/Frame 014576/0990 →