HRID232859

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7370

Benzenesulfonamide

C6H7NO2S

结构：O=C(O)CSC1c2ccccc2COc2ccc(OCc3ccc4ccccc4n3)cc21

HCID23359214

未命名化合物

PRODUCTS

生成物

结构：O=C(CSC1c2ccccc2COc2ccc(OCc3ccc4ccccc4n3)cc21)NS(=O)(=O)c1ccccc1

HCID23359157

未命名化合物

PROCEDURE

实验过程

11-Carboxymethylthio-2-(quinolin-2-yl)methoxy-6,11-dihydrodibenz[b,e]oxepine and benzensulfonamide were used and reacted in the same manner as in Example 39 to obtain the title compound.

WORKUP

后处理

customreacted in the same manner as in Example 39

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-18e333f04868449a9b5d8ce46cbe459a
来源数据集: uspto-grants-1997_01
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05591752
来源说明: uspto-grants-1997_01

反应 SMILES

[C:1]([CH2:4][S:5][CH:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:10][O:9][C:8]2[CH:17]=[CH:18][C:19]([O:21][CH2:22][C:23]3[CH:32]=[CH:31][C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[N:24]=3)=[CH:20][C:7]1=2)([OH:3])=O.[C:33]1([S:39]([NH2:42])(=[O:41])=[O:40])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>>[C:33]1([S:39]([NH:42][C:1]([CH2:4][S:5][CH:6]2[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[CH2:10][O:9][C:8]3[CH:17]=[CH:18][C:19]([O:21][CH2:22][C:23]4[CH:32]=[CH:31][C:30]5[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=5)[N:24]=4)=[CH:20][C:7]2=3)=[O:3])(=[O:41])=[O:40])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1