The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 26, 2017

Filed:

Nov. 20, 2013
Applicant:

Biogen MA Inc., Cambridge, MA (US);

Inventors:

Hairuo Peng, Cambridge, MA (US);

Edward Yin-Shiang Lin, Cambridge, MA (US);

Jianhua Chao, Cambridge, MA (US);

Zhili Xin, Cambridge, MA (US);

Bin Ma, Cambridge, MA (US);

Kevin Guckian, Cambridge, MA (US);

Timothy Chan, Cambridge, MA (US);

Gnanasambandam Kumaravel, Cambridge, MA (US);

Arthur G. Taveras, Cambridge, MA (US);

Assignee:

BIOGEN MA INC., Cambridge, MA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C07D 211/22 (2006.01); C07D 213/74 (2006.01); C07D 401/12 (2006.01); C07D 237/22 (2006.01); C07D 239/47 (2006.01); C07D 207/08 (2006.01); C07D 211/56 (2006.01); C07D 211/62 (2006.01); C07D 295/15 (2006.01); C07D 295/155 (2006.01); C07D 211/70 (2006.01); A61K 31/451 (2006.01); A61K 31/4545 (2006.01); A61K 31/495 (2006.01); A61K 31/501 (2006.01); A61K 31/506 (2006.01); A61K 45/06 (2006.01); C07D 401/04 (2006.01); C07D 403/04 (2006.01);
U.S. Cl.
CPC ...
C07D 211/22 (2013.01); A61K 31/451 (2013.01); A61K 31/4545 (2013.01); A61K 31/495 (2013.01); A61K 31/501 (2013.01); A61K 31/506 (2013.01); A61K 45/06 (2013.01); C07D 207/08 (2013.01); C07D 211/56 (2013.01); C07D 211/62 (2013.01); C07D 211/70 (2013.01); C07D 213/74 (2013.01); C07D 237/22 (2013.01); C07D 239/47 (2013.01); C07D 295/15 (2013.01); C07D 295/155 (2013.01); C07D 401/04 (2013.01); C07D 401/12 (2013.01); C07D 403/04 (2013.01);
Abstract

Compounds of formula (I) wherein: X is —O—, —S(O)—, —CH—, or —NR—, wherein r is 0, 1, or 2; X, X, and Xare each independently CRor N; one of Xor Xis C and is attached by a single bond to -L-, and the other is CRor N, provided that no more than three of X, X, X, X or Xare N; Ring A is monocyclic Cscycloalkyl or a 5- to 6-membered monocyclic heterocyclyl comprising from 1 to 5 heteroatoms independently selected from N, S, or O; wherein Ring A is further optionally substituted with from 1 to 3 R; provided that Ring A is not morpholinyl, thiomorpholinyl or tetrahydro-2H-pyranyl; L is a bond, —O—, —NR—, —S(O)—, —CH—, or —C(O)—, wherein n is 0, 1, or 2; 1 2 Lis an Calkylene, Ccycloalkylene, —CH-L-, or a 3- to 8-membered heterocyclylene comprising 1 to 5; Ris Calkyl or a monocyclic Ccycloalkyl; wherein said Ccycloalkyl is substituted with at least one Rand may be optionally substituted with from 1 to 5 additional Rsubstituents, wherein Rfor each occurrence is independently selected; and Ris —C(O)OR, —C(O)N(R)—S(O)R, —S(O)OR, —C(O)NHC(O)R, —Si(O)OH, —B(OH), —N(R)S(O)R, —S(O)N(R), —O—P(O)(OR), or —P(O)(OR), —CN, —S(O)NHC(O)R, —C(O)NHS(O)R3, —C(O)NHOH, —C(O)NHCN, —CH(CF)OH, —C(CF)OH, or a selected heteroaryl or heterocyclyl; and pharmaceutically acceptable salts thereof, can modulate the activity of one or more SIP receptors and/or the activity of autotaxin (ATX).


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