HRID1049775

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID69112

Benzoyl chloride, 2-iodo-

C7H4ClIO

HCID117699123

未命名化合物

PRODUCTS

生成物

结构：CCc1cccc2c1NC(=O)CC(=O)N2c1ccc(NC(=O)c2ccccc2I)cc1

HCID117699072

未命名化合物

HCID117699123

未命名化合物

PROCEDURE

实验过程

By using 1-(4-aminophenyl)-6-ethyl-1H-benzo[b][1,4]diazepine-2,4(3H,5H)-dione, and 2-iodobenzoyl chloride, the title compound was obtained in the same manner as that of Example 1, (4).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0a55eda004b74b2d939eaebe7b62b22f
来源数据集: uspto-grants-2016_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09382236B2
来源说明: uspto-grants-2016_07

反应 SMILES

[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:14](=[O:15])[CH2:13][C:12](=[O:16])[NH:11][C:10]3[C:17]([CH2:21][CH3:22])=[CH:18][CH:19]=[CH:20][C:9]2=3)=[CH:4][CH:3]=1.[I:23][C:24]1[CH:32]=[CH:31][CH:30]=[CH:29][C:25]=1[C:26](Cl)=[O:27]>>[CH2:21]([C:17]1[C:10]2[NH:11][C:12](=[O:16])[CH2:13][C:14](=[O:15])[N:8]([C:5]3[CH:4]=[CH:3][C:2]([NH:1][C:26](=[O:27])[C:25]4[CH:29]=[CH:30][CH:31]=[CH:32][C:24]=4[I:23])=[CH:7][CH:6]=3)[C:9]=2[CH:20]=[CH:19][CH:18]=1)[CH3:22].[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:14](=[O:15])[CH2:13][C:12](=[O:16])[NH:11][C:10]3[C:17]([CH2:21][CH3:22])=[CH:18][CH:19]=[CH:20][C:9]2=3)=[CH:6][CH:7]=1