Trifluoromethylsulfonamide → N-(Trifluoromethanesulphonyl)-6-[N-(5-chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazin-3-carboxamide

反応式

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

参加物

反応物 2

HCID 79001Trifluoromethylsulfonamide

HCID 186932496-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylic acid

生成物 1

HCID 18693222N-(Trifluoromethanesulphonyl)-6-[N-(5-chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazin-3-carboxamide

出典と根拠

ORDレコード: ord-c64756f089924c80ae4317bef86ec4af
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…