HRID2301816

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COC(=O)c1ccc(N)c(NC(=O)c2ccc(C(C)(C)C)cc2)c1

HCID10687588

未命名化合物

HCID16227938

1H-Indazole-6-carboxylic acid

C8H6N2O2

结构：COC(=O)c1ccc(NC(=O)c2ccc3cn[nH]c3c2)c(N)c1

HCID86586447

未命名化合物

PRODUCTS

生成物

结构：COC(=O)c1ccc(NC(=O)c2ccc3cn[nH]c3c2)c(NC(=O)c2ccc(C(C)(C)C)cc2)c1

HCID12015827

未命名化合物

PROCEDURE

实验过程

By methods substantially equivalent to those described in Example 9-C, N2-(4-t-butylbenzoyl)]-N1-(6-indazolylcarbonyl)-4-methoxycarbonyl-1,2-benzenediamine (0.1 g, 5%) was prepared from 4-methoxycarbonyl-N2-(4-t-butylbenzoyl)-1,2-benzenediamine and 6-indazolecarboxylic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-27990e329a674fb2b3fe7c31afed29ea
来源数据集: uspto-grants-2002_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06500851B2
来源说明: uspto-grants-2002_12

反应 SMILES

[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:10]([NH:12][C:13]3[C:14]([NH2:23])=[CH:15][C:16]([C:19]([O:21][CH3:22])=[O:20])=[CH:17][CH:18]=3)=[O:11])[CH:8]=2)[CH:3]=[N:2]1.COC(C1C=C(N[C:36](=[O:47])[C:37]2[CH:42]=[CH:41][C:40]([C:43]([CH3:46])([CH3:45])[CH3:44])=[CH:39][CH:38]=2)C(N)=CC=1)=O.N1C2C(=CC=C(C(O)=O)C=2)C=N1>>[C:43]([C:40]1[CH:39]=[CH:38][C:37]([C:36]([NH:23][C:14]2[C:13]([NH:12][C:10]([C:7]3[CH:8]=[C:9]4[C:4]([CH:3]=[N:2][NH:1]4)=[CH:5][CH:6]=3)=[O:11])=[CH:18][CH:17]=[C:16]([C:19]([O:21][CH3:22])=[O:20])[CH:15]=2)=[O:47])=[CH:42][CH:41]=1)([CH3:46])([CH3:44])[CH3:45]