4-(Difluoromethyl)-1,3-thiazol-2-amine → HCID 24820902、化合物
反応式
C(O[C:4]([C:6]1[CH:11]=[C:10]([C:12]2[CH:17]=[C:16]([F:18])[CH:15]=[C:14]([F:19])[CH:13]=2)[CH:9]=[C:8]([CH3:20])[N:7]=1)=[O:5])C.[F:21][CH:22]([F:29])[C:23]1[N:24]=[C:25]([NH2:28])[S:26][CH:27]=1>>[F:21][CH:22]([F:29])[C:23]1[N:24]=[C:25]([NH:28][C:4]([C:6]2[CH:11]=[C:10]([C:12]3[CH:13]=[C:14]([F:19])[CH:15]=[C:16]([F:18])[CH:17]=3)[CH:9]=[C:8]([CH3:20])[N:7]=2)=[O:5])[S:26][CH:27]=1参加物
3
実験手順
The title compound, was prepared from 4-(3,5-Difluorophenyl)-6-methyl-pyridine-2-carboxylic acid ethyl ester in accordance with the general method of example 26, step 6 using 4-Difluoromethyl-thiazol-2-ylamine instead of 3-chloroaniline to yield the final compound as a white solid, MS (ISP): m/e=382 [M]+.
出典と根拠
- ORDレコード
- ord-481fe5c6f9f84994a860179fdbc6222b
- 出典データセット
- uspto-grants-2011_05
- 特許番号