IP Library Granted Patent US 9,517,989
Granted Patent B2
US 9,517,989 · App. 14/436,865 · Granted Dec 13, 2016

2-cycloalkyl resorcinol cannabinergic ligands

Inventors: Alexandros Makriyannis (Watertown, MA); Marsha R. D'Souza (Boston, MA); Shama Bajaj (Somerville, MA); Spyridon P. Nikas (Waltham, MA); Ganeshsingh A. Thakur (Cambridge, MA)
Assignee: NORTHEASTERN UNIVERSITY
C07C39/23C07C39/42C07C43/168C07C43/1788C07C47/27C07C47/46C07C49/603C07C49/747C07C62/32C07C69/16C07C69/18C07C69/63C07C235/40C07C245/24C07C247/06C07C255/36C07C255/38C07D295/092C07D295/096C07D295/192C07D309/06C07D311/78C07D339/06C07C2101/02C07C2101/04C07C2101/08C07C2101/14C07C2101/16C07C2102/42C07C2103/04C07C2103/74
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Quick Facts
Patent No.
US 9,517,989
App. No.
14/436,865
Granted
Dec 13, 2016
Kind
B2
Abstract

The present invention relates to novel 2-cycloalkyl resorcinol compounds; to pharmaceutical compositions comprising the compounds; and to methods of preparing the compounds and uses thereof. The disclosed compounds can bind to and modulate the cannabinoid receptors and thus, they are specific ligands for these receptors. The invented compounds, when administered in a therapeutically effective amount to an individual or animal, results in a sufficiently high level of that compound in the individual or animal to cause a physiological response. The physiological response may be useful to treat a number of physiological conditions.

Claims (31)

1. A compound of formula I or a pharmaceutically acceptable salt thereof, including all stereoisomers and enantiomers:

wherein:

R 1 and R 2 are each independently selected from the group consisting of: —H, —F, —Cl, —Br, —I, —OH, —SH, —NH 2 , —NO 2 , —CN, —CF 3 , —OC(O)CH 3 , —C(O)CH 3 , —C(O)CF 3 , —O-alkyl, OSi(alkyl) 3 , —S— alkyl, —NH-alkyl, —N(alkyl) z , —O—P(O)(OR) 2 , —O—P(O)(OH)(OR) (wherein R is selected from the group consisting of H and alkyl), —P(O)(OR) 2 , —P(O)(OH)(OR) (wherein R is selected from the group consisting of H and alkyl), —O-alkyl-COOR (wherein R is selected from the group consisting of H and alkyl), —O-alkyl-NR 6 R 7 , —O-alkyl-CONR 6 R 7 , —OC(O)—R (wherein R is selected from the group consisting of H and alkyl), —OC(O)—CH(OH)—CH 2 OH, —OC(O)—C(CH 2 OH) 2 —CH 3 , —OC(O)—CH 2 OH, —OC(O)-alkyl-COOH, —OC(O)—CH═CHCOOH, —OC(O)-alkyl-NR 6 R 7 , —OC(O)-alkyl-C(O)NR 6 R 7 , —OC(O)—O-alkyl-NR 6 R 7 , and —OC(O)—CH(NH 2 )—R 8 (wherein R 8 is selected from the group consisting of H, CH(OH)CH 3 and alkyl-X 1 , and X 1 is selected from the group consisting of: —H, —NHC(═NH)NH 2 , —C(O)NH 2 , —COOH, —SH, —SCH 3 , —OH, —NH 2 , and an aromatic, heteroaromatic or heterocyclic ring);

R 6 and R 7 are each independently selected from the group consisting of: H and alkyl, or R 6 and R 7 together comprise part of a 3 to 7 membered saturated heterocyclic ring containing up to one additional heteroatom selected from the group consisting of N, O and S;

R 3 is selected from the group consisting of: -cycloalkyl-R 9 , -heterocyclic-R 9 , -adamantyl, -adamantyl-R 9 , and -heteroadamantyl-R 9 ;

R 9 is selected from the group consisting of: —(CH 2 ) j —R 10 , —(CH) j -A-(CH 2 ) k —R 10 , and —(CH 2 ) j -A-(CH 2 ) k —B—R 10 ;

A and B are each independently selected from the group consisting of: —CH 2 —CH 2 —, —C≡C—, —CH═CH—, —O—, —S—, —NH—, —C(O)—, —C(O)O—, —OC(O)—, —C(O)NH—, —NHC(O)—, —S(O)—, —SO 2 —, —SO 2 NH—, —NHSO 2 —, —SO 2 O— and —OSO 2 —;

R 10 is selected from the group consisting of: —H, —F, —Cl, —Br, —I, —OH, —SH, —NH 2 , —CN, —N 3 , —NCS, —NCO, —SO 2 Cl, —SO 2 F, —SO 2 NH 2 , —C(O)NH 2 , —COOH, —NO 2 , —CHO, —CF 3 , —SO 3 H, —O—P(O)(OH) 2 , —Sn(alkyl) 3 , —Si(alkyl) 3 , —C≡CH, —CH═CH 2 , and an aromatic, heteroaromatic or heterocyclic ring;

j is an integer from 0 to 8;

k is an integer from 0 to 8;

R 4 is selected from the group consisting of: -alkyl-R 11 , and —C 1-3 alkyl-OC(O)-alkyl;

R 11 is selected from the group consisting of: —F, —Cl, —Br, —I, —OH, —SH, —NH 2 , —NH-alkyl, —N(alkyl) 2 , —CN, —N 3 , —NCS, —OC(O)CH 3 , —C(O)OCH 3 , —SO 2 NH 2 , —C(O)NH 2 , —COOH, —NO 2 , —CHO, —CF 3 , —Sn(alkyl) 3 , —Si(alkyl) 3 , —C≡CH, —CH═CH 2 , and an aromatic, heteroaromatic or heterocyclic ring;

R 5 is selected from the group consisting of: —H, -alkyl, -alkyl-R 12 , -alkenyl, -alkenyl-R 12 , -alkynyl and -alkynyl-R 12 ; and

R 12 is selected from the group consisting of: —F, —Cl, —Br, —I, —OH, —SH, —NH 2 , —NH-alkyl, —N(alkyl) 2 , —CN, —N 3 , —NCS, —OC(O)CH 3 , —C(O)OCH 3 , —SO 2 NH 2 , —C(O)NH 2 , —COOH, —NO 2 , —CHO, —CF 3 , —Sn(alkyl) 3 , —Si(alkyl) 3 , —C≡CH, —CH═CH 2 , —(CH 2 ) n -Q (wherein Q is selected from the group consisting of —F, —Cl, —Br, —I, —OH, and n is an integer from 1 to 5), and an aromatic, heteroaromatic or heterocyclic ring.

2. The compound of claim 1 , wherein each of R 1 and R 2 are independently selected from the group consisting of —H, —SH, —NH 2 , —OH, —O-alkyl, —OSi(alkyl) 3 , —OC(O)CH 3 , and —O— alkyl-COOR (wherein R is selected from the group consisting of H and alkyl).

3. The compound of claim 2 , wherein R 1 and R 2 are —OH.

4. The compound of claim 1 , wherein R 3 is selected from the group consisting of -cycloalkyl-R 9 , -heterocyclyl-R 9 and -adamantyl.

5. The compound of claim 4 , wherein R 3 is selected from the group consisting of -cycloalkyl-R 9 and -heterocyclyl-R 9 , and R 9 is selected from the group consisting of —(CH 2 ) j -A-(CH 2 ) k —R 10 and —(CH 2 ) j -A-(CH 2 ) k —B—R 10 .

6. The compound of claim 5 , wherein R 9 is —(CH 2 ) j -A-(CH 2 ) k —R 10 .

7. The compound of claim 5 , wherein R 9 is —(CH 2 ) j -A-(CH 2 ) k —B—R 10 .

8. The compound of claim 6 , wherein A is selected from the group consisting of —CH 2 —CH 2 —, —CH═CH—, —C≡C—, —O—, —S—, —NH—, —C(O)—, —C(O)O—, —C(O)NH— and —NHC(O)—.

9. The compound of claim 8 , wherein A is selected from the group consisting of —CH 2 —CH 2 — and —CH═CH—.

10. The compound of claim 7 , wherein each of A and B are independently selected from the group consisting of —CH 2 —CH 2 —, —CH═CH—, —C≡C—, —O—, —S—, —NH—, —C(O)—, —C(O)O—, —C(O)NH— and —NHC(O)—.

11. The compound of claim 10 , wherein each of A and B are independently selected from the group consisting of —CH 2 —CH 2 — and —CH═CH—.

12. The compound of claim 1 , wherein R 10 is selected from the group consisting of —H, —F, —Cl, —Br, —I, —OH, —SH, —NH 2 , —CN, and —N 3 .

13. The compound of claim 1 , wherein j is selected from the group consisting of 0, 5 and 6.

14. The compound of claim 1 , wherein k is selected from the group consisting of 1 and 3.

15. The compound of claim 1 , wherein R 11 is —OH.

16. The compound of claim 1 , wherein R 5 is -alkenyl.

17. The compound of claim 1 , wherein the compound is selected from the group consisting of:

18. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.

Assignments (1)
CONFIRMATORY LICENSE Recorded Dec 13, 2016
From: NORTHEASTERN UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040899/0715 →
Continuity (2)
Provisional Application 61714914 · Oct 17, 2012
Related Publication 20150274623A1 · Oct 1, 2015