发明名称 Piperidinyl monocarboxylic acids as S1P1 receptor agonists
摘要 The present invention relates to novel compounds acting as agonists at S1P (sphingosine-1-phosphate) receptors, compositions containing these compounds, use of these compounds in medicine and their process of preparation.;
申请公布号 US9266867(B2) 申请公布日期 2016.02.23
申请号 US201214111438 申请日期 2012.04.10
申请人 BIOPROJET;SUN PHARMA ADVANCED RESEARCH COMPANY LTD 发明人 Capet Marc;Berrebi-Bertrand Isabelle;Robert Philippe;Schwartz Jean-Charles;Lecomte Jeanne-Marie;Thennati Rajamannar;Pal Ranjan Kumar;Samanta Biswajit;Pillai Muthukumaran Natarajan;Desai Japan Nitinkumar;Rana Dijixa Chandubhai;Prajapati Kaushik Dhanjubhai;Pathak Sandeep Pankajbhai;Panchal Bhavesh M.;Aradhye Jayraj D.
分类号 C07D413/10;C07D271/06;A61K31/454;A61K45/06 主分类号 C07D413/10
代理机构 Stites & Harbison, PLLC 代理人 Schulman, Esq. B. Aaron;Stites & Harbison, PLLC
主权项 1. A compound of formula (I): wherein: Ar is a phenyl group optionally substituted by one or more identical or different group(s) selected from the group consisting of halogen, alkyl, cycloalkyl, —Oalkyl, and phenyl; R1 represents —X—(Y)n— where —X— is selected from the group consisting of -alkyl-, -alkenyl-, -alkynyl-, -aryl-, and -alkylaryl-,each Y, identical or different is selected from the group consisting of H, OH, halogen, —Oalkyl, —Oalkylaryl, —OalkylOalkyl, —Oaryl, heteroaryl, —Oaryl(Oalkyl), —Ocycloalkyl, -cycloalkyl, and heterocyclyl;n is 1 to 3; and where R1 is not —C(═O)OH; and R2 is H or alkyl; or one of its stereoisomers or salts thereof.
地址 Paris FR