HRID2284131

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11264599

未命名化合物

结构：CN1CCN(c2ccc(C(=O)Nc3ccc([N+](=O)[O-])c([N+](=O)[O-])c3)cc2)CC1

HCID86673957

未命名化合物

PRODUCTS

生成物

结构：CN1CCN(c2ccc(C(=O)Nc3ccc4[nH]c(-c5ccc(C(=O)Nc6ccccc6)cc5)nc4c3)cc2)CC1

HCID178480673

未命名化合物

PROCEDURE

实验过程

Compound 216 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-(1-methyl-4-piperazinyl)benzamide and 4-phenylaminocarbonylbenzaldehyde. [M+H]+ calcd for C32H30N6O2: 531.25; found: 531.05.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fe8ded217f6a410f95c3ee805e7fca2a
来源数据集: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09144557B2
来源说明: uspto-grants-2015_09

反应 SMILES

[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:28])[C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][N:24]([CH3:27])[CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[C:29]1([NH:35][C:36]([C:38]2[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=2)=[O:37])[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>>[CH3:27][N:24]1[CH2:25][CH2:26][N:21]([C:18]2[CH:19]=[CH:20][C:15]([C:14]([NH:13][C:6]3[CH:7]=[CH:8][C:9]4[NH:10][C:42]([C:41]5[CH:40]=[CH:39][C:38]([C:36](=[O:37])[NH:35][C:29]6[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=6)=[CH:45][CH:44]=5)=[N:1][C:4]=4[CH:5]=3)=[O:28])=[CH:16][CH:17]=2)[CH2:22][CH2:23]1