HRID2115492

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CN(C)c1cccc(N(CC(=O)O)S(=O)(=O)c2ccc(C(C)(C)C)cc2)c1

HCID58978433

未命名化合物

HCID58978434

未命名化合物

PRODUCTS

生成物

结构：CCN(Cc1cccc(N(C)C)n1)C(=O)CN(c1cccc(N(C)C)c1)S(=O)(=O)c1ccc(C(C)(C)C)cc1

HCID58978377

未命名化合物

PROCEDURE

实验过程

prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-(3-dimethylamino-phenyl)-amino]-acetic acid with (6-ethylaminomethyl-pyridin-2-yl)-dimethyl-amine

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-02c9c6ab31e04325b197f65d93fea7bd
来源数据集: uspto-grants-2008_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07435815B2
来源说明: uspto-grants-2008_10

反应 SMILES

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