HRID1393603

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7398

Benzenesulfonyl chloride, 4-chloro-

C6H4Cl2O2S

结构：COC(=O)CCCCCNc1ccc2c(c1)nc(-c1ccccc1)n2-c1ccccc1

HCID67364955

未命名化合物

PRODUCTS

生成物

结构：COC(=O)CCCCCN(c1ccc2c(c1)nc(-c1ccccc1)n2-c1ccccc1)S(=O)(=O)c1ccc(Cl)cc1

HCID67366000

未命名化合物

PROCEDURE

实验过程

6-[[1,2-Diphenyl-1H-benzimidazol-5-yl]amino]hexanoic acid methyl ester was reacted with 4-chlorobenzenesulfonic acid chloride according to general operating instructions 13.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0d892cff9fc049f987173613fab9758b
来源数据集: uspto-grants-2008_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07345075B2
来源说明: uspto-grants-2008_03

反应 SMILES

[CH3:1][O:2][C:3](=[O:31])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][NH:9][C:10]1[CH:30]=[CH:29][C:13]2[N:14]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[N:16][C:12]=2[CH:11]=1.[Cl:32][C:33]1[CH:38]=[CH:37][C:36]([S:39](Cl)(=[O:41])=[O:40])=[CH:35][CH:34]=1>>[CH3:1][O:2][C:3](=[O:31])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][N:9]([S:39]([C:36]1[CH:37]=[CH:38][C:33]([Cl:32])=[CH:34][CH:35]=1)(=[O:41])=[O:40])[C:10]1[CH:30]=[CH:29][C:13]2[N:14]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:15]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)=[N:16][C:12]=2[CH:11]=1