HRID2284113

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CN(C)c1ccc(C(=O)Nc2ccc([N+](=O)[O-])c([N+](=O)[O-])c2)cc1

HCID86673952

未命名化合物

HCID86673954

未命名化合物

PRODUCTS

生成物

结构：CN(C)c1ccc(NC(=O)c2ccc(-c3nc4cc(NC(=O)c5ccc(N(C)C)cc5)ccc4[nH]3)cc2)cc1

HCID178482869

未命名化合物

PROCEDURE

实验过程

Compound 193 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-dimethylaminobenzoyl)aniline and 4-(4-dimethylaminophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C31H30N6O2: 519.24; found: 519.04.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c7aee3f2611f406e96e944836fa67dfb
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]([CH:19]=[CH:20][C:21]=1[N+:22]([O-])=O)[NH:7][C:8](=[O:18])[C:9]1[CH:14]=[CH:13][C:12]([N:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=1)([O-])=O.[CH3:25][N:26]([CH3:44])[C:27]1[CH:32]=[CH:31][C:30]([NH:33][C:34]([C:36]2[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=2)=[O:35])=[CH:29][CH:28]=1>>[CH3:16][N:15]([CH3:17])[C:12]1[CH:13]=[CH:14][C:9]([C:8]([NH:7][C:6]2[CH:19]=[CH:20][C:21]3[NH:22][C:40]([C:39]4[CH:38]=[CH:37][C:36]([C:34](=[O:35])[NH:33][C:30]5[CH:31]=[CH:32][C:27]([N:26]([CH3:44])[CH3:25])=[CH:28][CH:29]=5)=[CH:43][CH:42]=4)=[N:1][C:4]=3[CH:5]=2)=[O:18])=[CH:10][CH:11]=1