HRID2284114

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(N2CCOCC2)cc1

HCID86673955

未命名化合物

结构：O=Cc1ccc(C(=O)Nc2ccc(N3CCOCC3)cc2)cc1

HCID86673975

未命名化合物

PRODUCTS

生成物

结构：O=C(Nc1ccc(N2CCOCC2)cc1)c1ccc(-c2nc3cc(NC(=O)c4ccc(N5CCOCC5)cc4)ccc3[nH]2)cc1

HCID178522196

未命名化合物

PROCEDURE

实验过程

Compound 195 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-morpholin-4-ylbenzoyl)aniline and 4-(4-morpholinylphenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C35H34N6O4: 603.26; found: 603.36.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-6baa4ec936a84b2f9506697ead3a02b6
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:22]=[CH:23][C:24]=1[N+:25]([O-])=O)[NH:7][C:8](=[O:21])[C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)=[CH:11][CH:10]=1)([O-])=O.[N:28]1([C:34]2[CH:39]=[CH:38][C:37]([NH:40][C:41]([C:43]3[CH:50]=[CH:49][C:46]([CH:47]=O)=[CH:45][CH:44]=3)=[O:42])=[CH:36][CH:35]=2)[CH2:33][CH2:32][O:31][CH2:30][CH2:29]1>>[O:18]1[CH2:19][CH2:20][N:15]([C:12]2[CH:13]=[CH:14][C:9]([C:8]([NH:7][C:6]3[CH:22]=[CH:23][C:24]4[NH:25][C:47]([C:46]5[CH:49]=[CH:50][C:43]([C:41](=[O:42])[NH:40][C:37]6[CH:38]=[CH:39][C:34]([N:28]7[CH2:29][CH2:30][O:31][CH2:32][CH2:33]7)=[CH:35][CH:36]=6)=[CH:44][CH:45]=5)=[N:1][C:4]=4[CH:5]=3)=[O:21])=[CH:10][CH:11]=2)[CH2:16][CH2:17]1