4-Aminobenzyl alcohol → (4-(4-Chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)methanol

反応式

[Cl:1][c:2]1[n:3][c:4]([NH:12][c:13]2[cH:14][cH:15][c:16]([CH:19]([NH:20][C:21](=[O:22])[O:23][C:24]([CH3:25])([CH3:26])[CH3:27])[CH3:28])[cH:17][cH:18]2)[n:5][cH:6][c:7]1[C:8]([F:9])([F:10])[F:11].[NH2:29][c:30]1[cH:31][cH:32][c:33]([CH2:34][OH:35])[cH:36][cH:37]1>>[Cl:1][c:2]1[n:3][c:4]([NH:12][c:13]2[cH:14][cH:15][c:16]([CH2:34][OH:35])[cH:17][cH:18]2)[n:5][cH:6][c:7]1[C:8]([F:9])([F:10])[F:11]

参加物

反応物 2

HCID 693314-Aminobenzyl alcohol

HCID 76611269Tert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate

生成物 1

HCID 57584696(4-(4-Chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)methanol

出典と根拠

ORDレコード: ord-dce2ec02919c434092d82621bc3d744b
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…