产量(工程)
水杨酰胺
钥匙(锁)
过程(计算)
化学
计算机科学
组合化学
有机化学
材料科学
计算机安全
操作系统
冶金
作者
Abdullajon Odilov,Yin Liu,Tianwen Hu,Xiangrui Jiang,Jin Suo,Guanghui Tian,Feipu Yang,Jingshan Shen
标识
DOI:10.1021/acs.oprd.1c00184
摘要
An improved synthesis of simmerafil, a potent PDE5 inhibitor as a clinical candidate, is described with a 38.1% overall yield and 99.7% purity. Starting from the safe and inexpensive salicylamide (15), the key intermediate 2-propoxybenzimidamide (21), which is also a potential precursor for the preparation of pyrimidinone derivatives, was effectively and conveniently obtained. The subsequent process from 21 to simmerafil was optimized, which makes it more amenable to scale-up.
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