Substituted bicyclic compounds

US9770459B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9770459-B2
Application numberUS-201615337843-A
CountryUS
Kind codeB2
Filing dateOct 28, 2016
Priority dateAug 20, 2014
Publication dateSep 26, 2017
Grant dateSep 26, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Disclosed are compounds of Formulas (I), (II), (III), (IV), and (V): and/or a salt thereof, wherein R 1 is —OH or —OP(O)(OH) 2 , and X 1 , X 2 , X 3 , R 2 , R 2a , R a , R b , and R c are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P 1 , and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for treating an autoimmune disease or a chronic inflammatory disease, comprising administering to a mammalian patient a compound, wherein said autoimmune disease and chronic inflammatory disease is selected from systemic lupus erythematosis, multiple sclerosis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, rheumatoid arthritis, scleroderma, giant cell arteritis, and Sjogren's syndrome, wherein said compound is or salt there of; wherein R 1 is —OH or —OP(O)(OH) 2 . R 2 is R 2a or R 2b ; represents either a single bond to R 2a or a double bond to R 2b ; R 2a is —(CH 2 ) 3-6 CH 3 , —(CH 2 ) 1-4 CH═CR x R x , —(CH 2 ) 1-4 CH═CR x (CH 2 CH 3 , —CH═CH(CH 2 ) 1-3 C(R x ) 3 , —CH═CH(CH 2 ) 1-3 OCH 3 , —(CH 2 ) 1-3 CH═CHCH═CR x R x , —CH═CH(CH 2 ) 1-3 CH═CR x R x , —CH═CHR z , —(CH 2 ) 1-3 R z , —(CH 2 ) 1-3 O(CH 2 ) 0-3 R z , —(CH 2 ) 1-3 S(CH 2 ) 0-3 R z , —CH 2 S(O)R z , —CH 2 S(O) 2 R z , —O(CH 2 ) 1-2 R z , —O(CH 2 ) 1-2 O(CH 2 ) 0-2 R z , —OC(O)R z , —(CH 2 ) 1-4 O(CH 2 ) 0-9 C(R x ) 3 , —(CH 2 ) 1-4 O(CH 2 ) 0-9 CF 3 , —(CH 2 ) 1-4 CR x R x O(CH 2 ) 0-4 C(R x ) 3 , —(CH 2 ) 1-3 O(CH 2 ) 1-4 CH═CR x (CH 2 ) 0-3 CH 3 , —(CH 2 ) 1-3 O(CH 2 ) 1-4 CH═CR x R x , —(CH 2 ) 1-3 O(CH 2 ) 1-4 C(OH)R x R x , —(CH 2 ) 1-3 O(CH 2 ) 1-4 O(CH 2 ) 0-3 CH 3 , —(CH 2 ) 1-3 S(CH 2 ) 0-4 C(R x ) 3 , —(CH 2 ) 0-3 O(CH 2 ) 1-4 S(CH 2 ) 0-3 C(R x ) 3 , —(CH 2 ) 1-3 S(CH 2 ) 1-4 Si(CH 3 ) 3 , —(CH 2 ) 1-3 S(O)(CH 2 ) 0-4 C(R x ) 3 , —(CH 2 ) 1-3 S(O) 2 (CH 2 ) 0-4 C(R x ) 3 , —(CH 2 ) 1-5 NR x R x , —O(CH 2 ) 1-7 C(R x ) 3 , —O(CH 2 ) 1-4 O(CH 2 ) 0-4 C(R x ) 3 , —O(CH 2 ) 1-4 CH═CR x (CH 2 ) 0-3 CH 3 , —O(CH 2 ) 1-4 (CH 2 ) 0-3 C(R x ) 3 , —O(CH 2 ) 1-4 O(CH 2 ) 1-3 CH═CR x R x , —O(CH 2 ) 1-4 O(CH 2 ) 1-3 C≡CR x , —C(O)(CH 2 ) 0-4 C(R x ) 3 , —OC(O)(CH 2 ) 0-4 C(R x ) 3 , —OC(O)CR x R x (CH 2 ) 0-4 C(R x ) 3 , —OC(O)NR x (CH 2 ) 0-5 C(R x ) 3 , —NR x C(O)NR x (CH 2 ) 0-5 C(R x ) 3 , —C(CH 3 )═N—O(CH 2 ) 0-5 C(R x ) 3 , —C(CH 3) ═N—O(CH 2 ) 1-2 (phenyl), —C(CH 3 )═N—O(CH 2 ) 1-2 (fluorophenyl), —C(CH 3 )═N—O(CH 2 ) 1-2 (methoxyphenyl), phenyl, or pyridinyl; R 2b is (i) a 6-membered spiro-ring having one oxygen atom and substituted with R b , wherein R b is H or —(CH 2 ) 3 CH 3 ; or (ii) ═N—O—(CH 2 ) 3 CH 3 , ═N—O—CH 2 CH(CH 3 ) 2 , ═N—OCH 2 CH 2 (phenyl), or ═N—O—CH 2 CH 2 CH 2 (phenyl); R a is H each R b is H each R c is H, each R x is independently H or —CH 3 ; and R z is phenyl, imidazolyl, pyrazolyl, pyridinyl, pyrimidinyl, pyrazinyl, quinolinyl, thiophenyl, thiazolyl, oxetanyl, C 3-6 cycloalkyl, adamantanyl, or tetrahydropyranyl, each substituted with zero to 4 substituents independently selected from F, Cl, I, C 1-4 alkyl, —O(C 1-3 alkyl), —CF 3 , —OCF 3 , —(CH 2 ) 1-6 OCH 3 , —CH 2 NR x R x , —C(O)NR x R x , —C(O)NR x (C 1-4 alkyl), and —CH 2 C(O)NR x R x ; with the proviso that R 2 is not —(CH 2 ) 5 CH 3 wherein said autoimmune disease or chronic inflammatory disease is selected from systemic lupus erythematosis, multiple sclerosis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, rheumatoid arthritis, scleroderma, giant cell arteritis, and Sjögren's syndrome. 2. The method according to claim 1 wherein said compound is or a salt thereof. 3. The method according to claim 1 wherein said compound is or a salt thereof. 4. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is systemic lupus erythematosis. 5. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is ulcerative colitis. 6. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is multiple sclerosis. 7. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is inflammatory bowel disease. 8. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is rheumatoid arthritis. 9. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is Crohn's disease. 10. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is Sjögren's syndrome. 11. The method according to claim 3 wherein said autoimmune disease or chronic inflammatory disease is systemic lupus erythematosis. 12. The method according to claim 3 wherein said autoimmune disease or chronic inflammatory disease is ulcerative colitis. 13. The method according to claim 3 wherein said autoimmune disease or chronic inflammatory disease is multiple sclerosis. 14. The method according to claim 3 wherein said autoimmune disease or chronic inflammatory disease is inflammatory bowel disease. 15. The method according to claim 3 wherein said autoimmune disease or chronic inflammatory disease is rheumatoid arthritis. 16. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is Crohn's disease. 17. The method according to claim 2 wherein said autoimmune disease or chronic inflammatory disease is Sjögren's syndrome.

Assignees

Inventors

Classifications

  • Drugs for immunological or allergic disorders · CPC title

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • Immunomodulators · CPC title

  • Immunosuppressants, e.g. drugs for graft rejection · CPC title

  • Drugs for disorders of the cardiovascular system · CPC title

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What does patent US9770459B2 cover?
Disclosed are compounds of Formulas (I), (II), (III), (IV), and (V): and/or a salt thereof, wherein R 1 is —OH or —OP(O)(OH) 2 , and X 1 , X 2 , X 3 , R 2 , R 2a , R a , R b , and R c are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P 1 , and pharmaceutical compositions comprising such comp…
Who is the assignee on this patent?
Bristol Myers Squibb Co
What technology area does this patent fall under?
Primary CPC classification C07C217/74. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).