发明名称 |
Synthesis of Raltegravir |
摘要 |
The present invention relates to a novel synthetic route for the preparation of raltegravir and pharmaceutically acceptable salts, starting from 2-amino-2-methylpropanenitrile and oxadiazole carbonyl chloride, through the formation of a pyrimidinone intermediate of formula (V). |
申请公布号 |
US9475799(B1) |
申请公布日期 |
2016.10.25 |
申请号 |
US201615195477 |
申请日期 |
2016.06.28 |
申请人 |
Emcure Pharmaceuticals Limited |
发明人 |
Gurjar Mukund Keshav;Sonawane Swapnil Panditrao;Maikap Golakchandra Sudarshan;Patil Gulabrao Dagadu;Shinde Shivnath Bhaupatil;Shalikrao Pankaj;Mehta Samit Satish |
分类号 |
C07D271/10;C07D413/12 |
主分类号 |
C07D271/10 |
代理机构 |
Florek & Endres PLLC |
代理人 |
Florek & Endres PLLC |
主权项 |
1. A compound of formula: wherein R is CN; wherein R′ is H or CH3; wherein R2 is H and R3 is C1-4 alkyl group; or |
地址 |
IN |