HRID1029241

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID72896

Benzamide, N-(3-aminophenyl)-

C13H12N2O

结构：CN(C)CCNC(=O)c1ccc2c(=O)[nH]c3nccc(Cl)c3c2c1

HCID69810673

未命名化合物

PRODUCTS

生成物

结构：CN(C)CCNC(=O)c1ccc2c(=O)[nH]c3nccc(Nc4cccc(NC(=O)c5ccccc5)c4)c3c2c1

HCID69811630

未命名化合物

PROCEDURE

实验过程

The title compound was synthesized according to the procedure described for the preparation of Example 267 using 296 (40 mg, 0.12 mmol) and N-(3-amino-phenyl)-benzamide to provide 301. LC-MS (M+H=521, obsd.=521).

WORKUP

后处理

customThe title compound was synthesized

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e287c48075f84540a658f3b3ba548399
来源数据集: uspto-grants-2014_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08735584B2
来源说明: uspto-grants-2014_05

反应 SMILES

Cl[C:2]1[CH:11]=[CH:10][N:9]=[C:8]2[C:3]=1[C:4]1[CH:16]=[C:15]([C:17]([NH:19][CH2:20][CH2:21][N:22]([CH3:24])[CH3:23])=[O:18])[CH:14]=[CH:13][C:5]=1[C:6](=[O:12])[NH:7]2.[NH2:25][C:26]1[CH:27]=[C:28]([NH:32][C:33](=[O:40])[C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[CH:29]=[CH:30][CH:31]=1>>[C:33]([NH:32][C:28]1[CH:27]=[C:26]([NH:25][C:2]2[CH:11]=[CH:10][N:9]=[C:8]3[C:3]=2[C:4]2[CH:16]=[C:15]([C:17]([NH:19][CH2:20][CH2:21][N:22]([CH3:24])[CH3:23])=[O:18])[CH:14]=[CH:13][C:5]=2[C:6](=[O:12])[NH:7]3)[CH:31]=[CH:30][CH:29]=1)(=[O:40])[C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1