HRID2115489

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cc1ccc(N(CC(=O)O)S(=O)(=O)c2ccc(C(C)(C)C)cc2)cc1

HCID58978369

未命名化合物

HCID58978391

未命名化合物

PRODUCTS

生成物

结构：CCNc1cccc(CN(CC)C(=O)CN(c2ccc(C)cc2)S(=O)(=O)c2ccc(C(C)(C)C)cc2)n1

HCID58978406

未命名化合物

PROCEDURE

实验过程

prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-p-tolyl-amino]-acetic acid with ethyl-(6-ethylaminomethyl-pyridin-2-yl)-amine

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b8ea5d499e1b4933b6d086e2a99a39d2
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]([CH2:22][C:23]([OH:25])=O)[C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:26]([NH:28][C:29]1[CH:34]=[CH:33][CH:32]=[C:31]([CH2:35][NH:36][CH2:37][CH3:38])[N:30]=1)[CH3:27]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([C:15]2[CH:16]=[CH:17][C:18]([CH3:21])=[CH:19][CH:20]=2)[CH2:22][C:23]([N:36]([CH2:37][CH3:38])[CH2:35][C:31]2[CH:32]=[CH:33][CH:34]=[C:29]([NH:28][CH2:26][CH3:27])[N:30]=2)=[O:25])(=[O:12])=[O:13])=[CH:7][CH:6]=1)([CH3:2])([CH3:4])[CH3:3]