4-Sulfamoylthiobenzamide → 4-(6-Chloro-3a-hydroxy-8,8a-dihydro-3aH-indeno[1,2-d]thiazol-2-yl)benzenesulfonamide

HRID 275665

反応式

HRID 275665 の反応式
Br[CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:11])[CH:8]=2)[C:3]1=[O:12].[S:13]([C:17]1[CH:25]=[CH:24][C:20]([C:21]([NH2:23])=[S:22])=[CH:19][CH:18]=1)(=[O:16])(=[O:15])[NH2:14]>>[Cl:11][C:7]1[CH:6]=[CH:5][C:4]2[C:3]3([OH:12])[N:23]=[C:21]([C:20]4[CH:19]=[CH:18][C:17]([S:13]([NH2:14])(=[O:15])=[O:16])=[CH:25][CH:24]=4)[S:22][CH:2]3[CH2:10][C:9]=2[CH:8]=1

参加物

3

反応物 2

HCID 30032664-SulfamoylthiobenzamideHCID 113340692-Bromo-5-chloro-2,3-dihydro-1H-inden-1-one

生成物 1

HCID 98646914-(6-Chloro-3a-hydroxy-8,8a-dihydro-3aH-indeno[1,2-d]thiazol-2-yl)benzenesulfonamide

実験手順

4-(6-Chloro-3a-hydroxy-8,8a-dihydro-3aH-indeno[1,2-d]thiazol-2-yl)benzenesulfonamide is prepared in a similar manner by reacting 2-bromo-5-chloroindan-1-one with 4-sulfamoylthiobenzamide. The compound has a melting point of 160° C.

出典と根拠

ORDレコード
ord-e5b29e27975f438baf5df7248b349d71
出典データセット
uspto-grants-2002_03
特許番号
US06352987B2

関連ノート

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