HRID1883778

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3153997

4-(2,6-Dimethyl-piperidin-1-ylmethyl)-phenylamine

C14H22N2

结构：CCOC(=O)c1ccc2c(c1)N(C(C)=O)C(=O)C2=C(OCC)c1ccccc1

HCID68527561

Ethyl 1-acetyl-3-(ethoxyphenylmethylene)-2,3-dihydro-2-oxo-1H-indole-6-carboxylate

C22H21NO5

PRODUCTS

生成物

$结构：CCOC(=O)c1ccc2c(c1)NC(=O)/C2=C(\Nc1ccc(CN2C(C)CCCC2C)cc1)c1ccccc1$

HCID178468590

未命名化合物

PROCEDURE

实验过程

Prepared from 1-acetyl-3-(1-ethoxy-1-phenylmethylene)-6-ethoxycarbonyl-2-indolinone and 4-[(2,6-dimethyl-piperidin-1-yl)-methyl]-aniline Rf value: 0.6 (silica gel, methylene chloride/ethanol=5:1) C32H35N3O3

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-535e1970e69f483c85d91aca9095ec09
来源数据集: uspto-grants-2004_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06762180B1
来源说明: uspto-grants-2004_07

反应 SMILES

C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=2)[C:6](=[C:18](OCC)[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:5]1=[O:28])(=O)C.[CH3:29][CH:30]1[CH2:35][CH2:34][CH2:33][CH:32]([CH3:36])[N:31]1[CH2:37][C:38]1[CH:44]=[CH:43][C:41]([NH2:42])=[CH:40][CH:39]=1>>[CH3:36][CH:32]1[CH2:33][CH2:34][CH2:35][CH:30]([CH3:29])[N:31]1[CH2:37][C:38]1[CH:39]=[CH:40][C:41]([NH:42]/[C:18](=[C:6]2\[C:5](=[O:28])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=3)/[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:43][CH:44]=1