IP Library Granted Patent US 12,178,813
Granted Patent B2
US 12,178,813 · App. 17/139,299 · Granted Dec 31, 2024

CGRP receptor antagonists

Inventors: John Andrew Christopher (Cambridge, GB); Miles Stuart Congreve (Cambridge, GB); Sarah Joanne Bucknell (Cambridge, GB); Francesca Deflorian (Cambridge, GB); Mark Pickworth (Cambridge, GB); Jonathan Stephen Mason (Cambridge, GB)
Assignee: Nxera Pharma UK Limited
A61K31/496C07D241/14C07D401/14C07D471/04C07D498/10C07D498/20
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Quick Facts
Patent No.
US 12,178,813
App. No.
17/139,299
Granted
Dec 31, 2024
Kind
B2
Abstract

The disclosures herein relate to novel compounds of formula wherein R 1 , R 2 , R 3 and R 4 are as defined herein, and their use in treating, preventing, ameliorating, controlling or reducing cerebrovascular or vascular disorders associated with CGRP receptor function.

Claims (62)

1. A pharmaceutical composition comprising a) a compound of formula (I):

or a salt thereof, an optical isomer thereof, or a combination thereof,

wherein R 1 is H or Q-(C 1 -C 6 )alkyl; where Q is a bond, C(O) or C(O)O and where the (C 1 -C 6 )alkyl can be optionally substituted by N(C 1 -C 3 alkyl) 2 or CO 2 H;

R 2 is H or forms a spirocyclic heterocyclic ring with R 3 ;

R 3 forms a spirocyclic heterocyclic ring with R 2 or is a heterocyclic ring if R 2 is H; and

R 4 is an optionally substituted aryl group which may be monocyclic or fused to a further ring; and

b) one or more pharmaceutically acceptable carriers.

2. The pharmaceutical composition according to claim 1 wherein R 4 is a substituted phenyl group wherein the substituents are selected from halo or hydroxy.

3. The pharmaceutical composition according to claim 1 wherein R 4 is a moiety according to formula (II)

wherein X is halo.

4. The pharmaceutical composition according to claim 3 wherein X is Br.

5. The pharmaceutical composition according to claim 1 wherein R 4 is

6. The pharmaceutical composition according to claim 5 wherein R 4 is

7. The pharmaceutical composition according to claim 1 wherein R 2 is H and R 3 is:

8. The pharmaceutical composition according to claim 1 wherein R 2 forms a spirocyclic heterocyclic ring with R 3 to form:

9. The pharmaceutical composition according to claim 1 wherein R 2 is H or forms a spirocyclic heterocyclic ring with R 3 to form:

and wherein when R 2 is H, R 3 is:

10. The pharmaceutical composition according to claim 1 wherein R 1 is H, CO 2 t Bu, CH 2 CH 3 , CH 2 CH 2 CH 3 , COCH 2 CH 2 CH 2 CH 3 , CH 2 CH 2 N(CH 3 ) 2 , or COCH 2 CO 2 H.

11. The pharmaceutical composition according to claim 10 wherein R 1 is H.

12. The pharmaceutical composition according to claim 1 wherein the compound is selected from the group consisting of:

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide;

tert-butyl 4-{(2S)-2-{[(2R)-3-(7-methyl-1H-indazol-5-yl)-2-({[4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidin-1-yl]carbonyl}amino)propanoyl]amino}-3-oxo-3-[4-(pyridin-4-yl)piperazin-1-yl]propyl}piperidine-1-carboxylate;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(1-propylpiperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

3,5-dibromo-Nα-{[4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidin-1-yl]carbonyl}-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}-D-tyrosinamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(1-pentanoylpiperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

N-[(2R)-1-({(2S)-3-(1-ethylpiperidin-4-yl)-1-oxo-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

3,5-dibromo-Nα-{[4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidin-1-yl]carbonyl}-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}-D-tyrosinamide;

3,5-dibromo-Nα-{[4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidin-1-yl]carbonyl}-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}-D-tyrosinamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carboxamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-2′-oxo-1′,2′-dihydro-1H-spiro[piperidine-4,4′-pyrido[2,3-d][1,3]oxazine]-1-carboxamide;

N-[(2R)-1-({(2S)-3-{1-[2-(dimethylamino)ethyl]piperidin-4-yl}-1-oxo-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide;

3-(4-{(2S)-2-{[(2R)-3-(7-methyl-1H-indazol-5-yl)-2-({[4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidin-1-yl]carbonyl}amino)propanoyl]amino}-3-oxo-3-[4-(pyridin-4-yl)piperazin-1-yl]propyl}piperidin-1-yl)-3-oxopropanoic acid, ammonium salt; and

3,5-dibromo-Nα-[(2′-oxo-1′,2′-dihydro-1H-spiro[piperidine-4,4′-pyrido[2,3-d][1,3]oxazin}-1-yl)carbonyl]-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl[propan-2-yl}-D-tyrosinamide.

13. The pharmaceutical composition according to claim 12 wherein the compound is:

14. The pharmaceutical composition according to claim 1 , further comprising one or more ingredients selected from the group consisting of diluents, adjuvants, excipients, vehicles, preserving agents, fillers, disintegrating agents, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavouring agents, perfuming agents, antibacterial agents, antifungal agents, lubricating agents, and dispersing agents.

15. The pharmaceutical composition according to claim 1 , wherein said composition is in the form of a tablet, dragee, powder, elixir, syrup or liquid preparation.

16. The pharmaceutical composition according to claim 1 , wherein said composition is in the form of a suspension, spray, inhalant, tablet, lozenge, emulsion, solution, cachet, granule, capsule, or suppository.

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

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide;

tert-butyl 4-{(2S)-2-{[(2R)-3-(7-methyl-1H-indazol-5-yl)-2-({[4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidin-1-yl]carbonyl}amino)propanoyl]amino}-3-oxo-3-[4-(pyridin-4-yl)piperazin-1-yl]propyl}piperidine-1-carboxylate;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(1-propylpiperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

3,5-dibromo-Nα-{[4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidin-1-yl]carbonyl}-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}-D-tyrosinamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(1-pentanoylpiperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

N-[(2R)-1-({(2S)-3-(1-ethylpiperidin-4-yl)-1-oxo-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl]-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide;

3,5-dibromo-Nα-{[4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidin-1-yl]carbonyl}-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}-D-tyrosinamide;

3,5-dibromo-Nα-{[4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidin-1-yl]carbonyl}-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}-D-tyrosinamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carboxamide;

N-[(2R)-3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-({(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)propan-2-yl]-2′-oxo-1′,2′-dihydro-1H-spiro[piperidine-4,4′-pyrido[2,3-d][1,3]oxazine]-1-carboxamide;

N-[(2R)-1-({(2S)-3-{1-[2-(dimethylamino)ethyl]piperidin-4-yl}-1-oxo-1-[4-(pyridin-4-yl)piperazin-1-yl]propan-2-yl}amino)-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide;

3-(4-{(2S)-2-{[(2R)-3-(7-methyl-1H-indazol-5-yl)-2-({[4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidin-1-yl]carbonyl}amino)propanoyl]amino}-3-oxo-3-[4-(pyridin-4-yl)piperazin-1-yl]propyl}piperidin-1-yl)-3-oxopropanoic acid, ammonium salt; and

3,5-dibromo-Nα-[(2′-oxo-1′,2′-dihydro-1H-spiro[piperidine-4,4′-pyrido[2,3-d][1,3]oxazin}-1-yl)carbonyl]-N-{(2S)-1-oxo-3-(piperidin-4-yl)-1-[4-(pyridin-4-yl)piperazin-1-yl[propan-2-yl}-D-tyrosinamide;

or a salt thereof, an optical isomer thereof, or a combination thereof.

18. The pharmaceutical composition according to claim 1 , wherein the compound is:

a salt thereof, an optical isomer thereof, or a combination thereof.

19. The pharmaceutical composition according to claim 1 , wherein the compound is:

20. The pharmaceutical composition according to claim 1 , wherein the compound is:

or a salt thereof, an optical isomer thereof, or a combination thereof.

21. The pharmaceutical composition according to claim 1 , wherein the compound is:

22. The pharmaceutical composition according to claim 1 , wherein the compound is:

or a salt thereof, an optical isomer thereof, or a combination thereof.

Assignments (2)
CHANGE OF NAME Recorded Sep 25, 2024
From: HEPTARES THERAPEUTICS LIMITED
To: NXERA PHARMA UK LIMITED
Reel/Frame 068695/0706 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2021
From: CHRISTOPHER, JOHN ANDREW; CONGREVE, MILES STUART; BUCKNELL, SARAH JOANNE; DEFLORIAN, FRANCESCA; PICKWORTH, MARK; MASON, JONATHAN STEPHEN
To: HEPTARES THERAPEUTICS LIMITED
Reel/Frame 056178/0679 →
Priority Claims (1)
GB 1519196 · Oct 30, 2015 · national
Continuity (4)
Continuation 16377519 · Apr 8, 2019
Continuation 15713775 · Sep 25, 2017
Division 15336866 · Oct 28, 2016
Related Publication 20210213011A1 · Jul 15, 2021