HRID2284144

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C(Nc1ccc([N+](=O)[O-])c([N+](=O)[O-])c1)c1ccc(N2CCCC2)cc1

HCID86673966

未命名化合物

HCID178434561

未命名化合物

PRODUCTS

生成物

结构：Cc1n[nH]cc1NC(=O)c1ccc(-c2nc3cc(NC(=O)c4ccc(N5CCCC5)cc4)ccc3[nH]2)cc1

HCID178434560

未命名化合物

PROCEDURE

实验过程

Compound 232 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide and 4-(3-methyl-4-pyrazolyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C29H27N7O2: 506.23; found: 506.25.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-231ffd9cdb3f4024af5fc27877042def
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:26])[C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:25][CH2:24][CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[CH3:27][C:28]1[C:32]([NH:33][C:34]([C:36]2[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=2)=[O:35])=[CH:31][NH:30][N:29]=1>>[CH3:27][C:28]1[C:32]([NH:33][C:34](=[O:35])[C:36]2[CH:43]=[CH:42][C:39]([C:40]3[NH:10][C:9]4[CH:8]=[CH:7][C:6]([NH:13][C:14](=[O:26])[C:15]5[CH:20]=[CH:19][C:18]([N:21]6[CH2:25][CH2:24][CH2:23][CH2:22]6)=[CH:17][CH:16]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:38][CH:37]=2)=[CH:31][NH:30][N:29]=1