Ethanesulfonamide → Ethanesulfonamide

反応式

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

参加物

反応物 3

HCID 73702Ethanesulfonamide

HCID 441195946-Chloro-1-methyl-1H-indole-2-boronic acid

HCID 66788384N-(5-bromopyridin-3-yl)ethanesulfonamide

生成物 2

HCID 73702Ethanesulfonamide

HCID 58215662N-[5-(6-chloro-1-methylindol-2-yl)-3-pyridinyl]ethanesulfonamide

出典と根拠

ORDレコード: ord-9288666ab8c44251bbfe499b6c5fec0a
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…