IP Library Granted Patent US 11,319,312
Granted Patent B2
US 11,319,312 · App. 17/069,070 · Granted May 3, 2022

Pharmaceutical compounds

Inventors: Giles Albert Brown (Cambridge, GB); Barry John Teobald (Cambridge, GB); Benjamin Gerald Tehan (Cambridge, GB)
C07D413/14C07D451/02C07D451/14C07D453/06C07D471/10C07D487/10C07D491/08C07D498/08C07D498/10C07B2200/07C07B2200/09
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Quick Facts
Patent No.
US 11,319,312
App. No.
17/069,070
Granted
May 3, 2022
Kind
B2
Abstract

This invention relates to compounds that are agonists of the muscarinic M 1 and/or M 4 receptor and which are useful in the treatment of diseases mediated by the muscarinic M 1 and M 4 receptors. Also provided are pharmaceutical compositions containing the compounds and the therapeutic uses of the compounds. Compounds provided are of formula where X 1 ; X 2 ; X 3 ; X 4 ; R 1 R 2 and R 4 are as defined herein.

Claims (47)

1. A compound of formula (1):

or a salt thereof, wherein:

the ring system formed by X 1 and X 2 is selected from:

the ring system formed by X 3 and X 4 is selected from:

R 1 is CONR 5 R 6 ;

R 2 is selected from hydrogen, fluorine, cyano and a C 1-3 hydrocarbon group which is optionally substituted with one to six fluorine atoms;

R 4 is H or C 1-6 alkyl optionally substituted with one or more fluorine atoms;

R 5 is hydrogen or a non-aromatic C 1-10 hydrocarbon group optionally substituted with one or more fluorine atoms;

R 6 is hydrogen or a non-aromatic C 1-10 hydrocarbon group optionally substituted with one or more fluorine atoms.

2. The compound according to claim 1 which is a compound of formula (2):

or a salt thereof.

3. The compound according to claim 1 which is a compound of formula (3):

or a salt thereof.

4. The compound according to claim 1 , or a salt thereof, wherein the ring system formed by X 1 and X 2 is:

5. The compound according to claim 1 , or a salt thereof, wherein R 5 is methyl, ethyl or methylcyclobutyl.

6. The compound according to claim 1 , or a salt thereof, wherein R 5 is methylcyclobutyl.

7. The compound according to claim 1 , or a salt thereof, wherein R 6 is H, methyl, ethyl or methylcyclobutyl.

8. The compound according to claim 1 , or a salt thereof, wherein R 6 is H.

9. The compound according to claim 1 , or a salt thereof, wherein R 1 is selected from:

10. The compound according to claim 1 , or a salt thereof, wherein R 1 is:

11. The compound according to claim 1 , or a salt thereof, wherein R 2 is selected from H, methyl, cyano and F.

12. The compound according to claim 1 , or a salt thereof, wherein R 2 is H.

13. The compound according to claim 1 , or a salt thereof, wherein R 4 is methyl, trifluoromethyl, ethyl or isopropyl.

14. The compound according to claim 1 , which is selected from:

N-(1-Methylcyclobutyl)-1-[8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]oct-3-yl]piperidine-4-carboxamide;

(1R,5S,6r)-N,N-Diethyl-3-[9-(3-methyl-1,2,4-oxadiazol-5-yl)-3-oxa-9-azabicyclo[3.3.1]non-7-yl]-3-azabicyclo[3.1.0] hexane-6-carboxamide;

1-(8-(3-Methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-N-(1-(trifluoromethyl)cyclobutyl)piperidine-4-carboxamide;

N-(1-Ethylcyclobutyl)-1-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)piperidine-4-carboxamide;

N-(1-isopropylcyclobutyl)-1-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)piperidine-4-carboxamide;

1-(8-(3-Methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-N-(1-methylcyclopentyl)piperidine-4-carboxamide;

1-(8-(3-Methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-N-((1-methylcyclobutyl)methyl)piperidine-4-carboxamide;

(1R,5S,6r)-3-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-N-(1-methylcyclobutyl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

N-(1-Methylcyclobutyl)-1-(8-(3-(trifluoromethyl)-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)piperidine-4-carboxamide;

(1R,5S,6r)-N-isopropyl-N-methyl-3-(9-(3-methyl-1,2,4-oxadiazol-5-yl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

(1R,5S,6r)-N,N-diethyl-3-(9-(3-(trifluoromethyl)-1,2,4-oxadiazol-5-yl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

(1R,5S,6r)-N-ethyl-N-methyl-3-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

(1R,5S,6r)-N,N-diethyl-3-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

(1R,5S,6r)-N,N-dimethyl-3-(9-(3-(trifluoromethyl)-1,2,4-oxadiazol-5-yl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

(1R,5S,6r)-N-isopropyl-N-methyl-3-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

(1R,5S,6r)-3-(8-(3-methyl-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)-N-(1-(trifluoromethyl)cyclobutyl)-3-azabicyclo[3.1.0]hexane-6-carboxamide;

or a salt thereof.

15. The compound according to claim 1 , which is N-(1-Methylcyclobutyl)-1-(8-(3-(trifluoromethyl)-1,2,4-oxadiazol-5-yl)-8-azabicyclo[3.2.1]octan-3-yl)piperidine-4-carboxamide or a salt thereof.

16. The compound according to claim 1 , which is (1R,5S,6r)-N,N-diethyl-3-(9-(3-(trifluoromethyl)-1,2,4-oxadiazol-5-yl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-3-azabicyclo[3.1.0]hexane-6-carboxamide or a salt thereof.

17. A pharmaceutical composition comprising a compound according to claim 1 , or a salt thereof, and a pharmaceutically acceptable excipient.

18. A method of treating a cognitive disorder selected from Schizophrenia, Alzheimer's disease and dementia with Lewy bodies, or for the treatment or lessening the severity of acute, chronic, neuropathic, or inflammatory pain comprising administering an effective amount of a compound according to claim 1 , or a salt thereof, to a subject in need thereof.

19. The method according to claim 18 wherein the cognitive disorder is Alzheimer's disease.

20. The method according to claim 18 wherein the cognitive disorder is dementia with Lewy bodies.

Assignments (3)
CHANGE OF NAME Recorded Sep 9, 2024
From: HEPTARES THERAPEUTICS LIMITED
To: NXERA PHARMA UK LIMITED
Reel/Frame 068524/0400 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 3, 2023
From: HEPTARES THERAPEUTICS LIMITED
To: ALLERGAN PHARMACEUTICALS INTERNATIONAL LIMITED; HEPTARES THERAPEUTICS LIMITED
Reel/Frame 065452/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2021
From: BROWN, GILES ALBERT; TEOBALD, BARRY JOHN; TEHAN, BENJAMIN GERALD
To: HEPTARES THERAPEUTICS LIMITED
Reel/Frame 054865/0858 →
Priority Claims (1)
GB 1810245 · Jun 22, 2018 · national
Continuity (2)
Continuation 16450279 · Jun 24, 2019
Related Publication 20210101893A1 · Apr 8, 2021
Cited By (3)
US 12,202,843 US 12,215,099 US 12,291,512