4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-oxazol-5-yl-benzenesulfonamide

反応式

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

参加物

反応物 2

HCID 27764154-(1,3-Oxazol-5-yl)benzenesulphonyl chloride

HCID 22327305(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanone

生成物 1

HCID 10389230N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-oxazol-5-yl-benzenesulfonamide

出典と根拠

ORDレコード: ord-dbde0c9801c242358ece1e97fb041f86
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…