1-(2-Hydroxyethyl)piperazine → Isopropyl 2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-formate
反応式
Br[C:2]1[N:7]=[C:6]([CH3:8])[N:5]=[C:4]([NH:9][C:10]2[S:11][C:12]([C:15]([O:17][CH:18]([CH3:20])[CH3:19])=[O:16])=[CH:13][N:14]=2)[CH:3]=1.[OH:21][CH2:22][CH2:23][N:24]1[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1>>[OH:21][CH2:22][CH2:23][N:24]1[CH2:29][CH2:28][N:27]([C:2]2[N:7]=[C:6]([CH3:8])[N:5]=[C:4]([NH:9][C:10]3[S:11][C:12]([C:15]([O:17][CH:18]([CH3:20])[CH3:19])=[O:16])=[CH:13][N:14]=3)[CH:3]=2)[CH2:26][CH2:25]1参加物
3
実験手順
Prepared from isopropyl 2-(6-bromo-2-methylpyrimidin-4-ylamino)thiazole-5-formate and Compound 3: isopropyl 2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-formate was yielded (yield: 77.2%).
出典と根拠
- ORDレコード
- ord-53ee88201cc24cbd94e69e6438ee6667
- 出典データセット
- uspto-grants-2015_08
- DOI