HRID2284277

反应详情

EQUATION

反应方程式

REACTANTS

反应物

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

HCID86673975

未命名化合物

结构：N#Cc1ccc(COc2ccc([N+](=O)[O-])c([N+](=O)[O-])c2)cc1

HCID86674011

未命名化合物

PRODUCTS

生成物

结构：N#Cc1ccc(COc2ccc3nc(-c4ccc(C(=O)Nc5ccc(N6CCOCC6)cc5)cc4)[nH]c3c2)cc1

HCID67686981

未命名化合物

PROCEDURE

实验过程

Compound 641 was prepared according to the procedure similar to that described in Scheme III from 1-(4-cyanobenzyloxy)-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C32H27N5O3: 530.21; found: 530.10.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-20b1d94e018b4f4dbb6d469cfd9cbcf3
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

[C:1]([C:3]1[CH:22]=[CH:21][C:6]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[C:11]([N+:18]([O-])=O)[CH:10]=2)=[CH:5][CH:4]=1)#[N:2].[O:23]1[CH2:28][CH2:27][N:26]([C:29]2[CH:34]=[CH:33][C:32]([NH:35][C:36]([C:38]3[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=3)=[O:37])=[CH:31][CH:30]=2)[CH2:25][CH2:24]1>>[C:1]([C:3]1[CH:22]=[CH:21][C:6]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]3[N:15]=[C:42]([C:41]4[CH:40]=[CH:39][C:38]([C:36]([NH:35][C:32]5[CH:31]=[CH:30][C:29]([N:26]6[CH2:25][CH2:24][O:23][CH2:28][CH2:27]6)=[CH:34][CH:33]=5)=[O:37])=[CH:45][CH:44]=4)[NH:18][C:11]=3[CH:10]=2)=[CH:5][CH:4]=1)#[N:2]