HRID2284159

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7071

3,3'-Diaminobenzidine

C12H14N4

HCID11264599

未命名化合物

PRODUCTS

生成物

结构：O=C(Nc1ccccc1)c1ccc(-c2nc3cc(-c4ccc5nc(-c6ccc(C(=O)Nc7ccccc7)cc6)[nH]c5c4)ccc3[nH]2)cc1

HCID136352326

未命名化合物

PROCEDURE

实验过程

Compound 261 was prepared according to the procedure similar to that described in Scheme III from 3,3′-diaminobenzidine and 4-phenylaminocarbonylbenzaldehyde. [M+H]+ calcd for C40H28N6O2: 625.23; found: 625.53.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7a8dddbb26ea451d80115cb98162a665
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

[NH2:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:15]=[CH:14][C:12]([NH2:13])=[C:11]([NH2:16])[CH:10]=2)[CH:5]=[CH:6][C:7]=1[NH2:8].[C:17]1([NH:23][C:24]([C:26]2[CH:33]=[CH:32][C:29]([CH:30]=O)=[CH:28][CH:27]=2)=[O:25])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[NH:8]1[C:7]2[CH:6]=[CH:5][C:4]([C:9]3[CH:15]=[CH:14][C:12]4[N:13]=[C:30]([C:29]5[CH:32]=[CH:33][C:26]([C:24]([NH:23][C:17]6[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=6)=[O:25])=[CH:27][CH:28]=5)[NH:16][C:11]=4[CH:10]=3)=[CH:3][C:2]=2[N:1]=[C:30]1[C:29]1[CH:28]=[CH:27][C:26]([C:24]([NH:23][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:25])=[CH:33][CH:32]=1