HRID274975

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=[N+]([O-])c1ccccc1-c1ccc(S(=O)(=O)Cl)cc1

HCID21806117

2′-Nitro[1,1′-biphenyl]-4-sulfonyl chloride

C12H8ClNO4S

结构：CC1CCN(C(=O)C(N)Cc2ccc3[nH]cnc3c2)CC1

HCID178428665

未命名化合物

PRODUCTS

生成物

结构：CC1CCN(C(=O)C(Cc2ccc3[nH]cnc3c2)NS(=O)(=O)c2ccc(-c3ccccc3[N+](=O)[O-])cc2)CC1

HCID178428643

未命名化合物

PROCEDURE

实验过程

Prepared from 1-(1H-benzimidazol-5-yl-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethylamine and 2'-nitro-4-biphenylyl-sulphonic acid chloride analogously to Example 2.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b9775ba961bb4e4da4112db7f80b3b39
来源数据集: uspto-grants-1995_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05391556
来源说明: uspto-grants-1995_02

反应 SMILES

[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH:11]([NH2:21])[C:12]([N:14]3[CH2:19][CH2:18][CH:17]([CH3:20])[CH2:16][CH2:15]3)=[O:13])=[CH:9][C:4]=2[N:3]=[CH:2]1.[N+:22]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[C:31]1[CH:36]=[CH:35][C:34]([S:37](Cl)(=[O:39])=[O:38])=[CH:33][CH:32]=1)([O-:24])=[O:23]>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH:11]([NH:21][S:37]([C:34]3[CH:33]=[CH:32][C:31]([C:26]4[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=4[N+:22]([O-:24])=[O:23])=[CH:36][CH:35]=3)(=[O:38])=[O:39])[C:12]([N:14]3[CH2:19][CH2:18][CH:17]([CH3:20])[CH2:16][CH2:15]3)=[O:13])=[CH:9][C:4]=2[N:3]=[CH:2]1