HRID1833507

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID16245296

未命名化合物

PRODUCTS

生成物

结构：Cc1c2c(c(-c3ccccc3)c(-c3ccccc3)c1-c1ccccc1)C(=N)NC2=C1SC(NCc2ccccc2)=NC1=N.Cl

HCID178421562

未命名化合物

PROCEDURE

实验过程

Using a procedure similar to that described in Example 9, part B above but substituting 4-methyl-5,6,7-triphenyl-1,3-diiminoisoindoline and 2-benzylamino-4-imino-2-thiazoline hydrochloride for the 1,3-diiminoisoindoline and 2-piperidino-4-imino-2-thiazoline hydrochloride respectively, there is obtained as the product 1-imino-4-methyl-5,6,7-triphenyl-3-(2benzylamino-4-imino-2-thiazolin-5-ylidene)isoindoline hydrochloride.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c88f61021e344224b55fda2924841148
来源数据集: uspto-grants-1978_01
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04066653
来源说明: uspto-grants-1978_01

反应 SMILES

[CH3:1][C:2]1[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:9]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:8]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:7]2[C:3]=1[C:4](=N)[NH:5][C:6]2=[NH:29].[ClH:31].[CH2:32]([NH:39][C:40]1[S:41][CH2:42][C:43](=[NH:45])[N:44]=1)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1.N=C1C2C(=CC=CC=2)C(=N)N1.Cl.N1(C2SCC(=N)N=2)CCCCC1>>[ClH:31].[NH:29]=[C:6]1[C:7]2[C:3](=[C:2]([CH3:1])[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[C:9]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:8]=2[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[C:4](=[C:42]2[S:41][C:40]([NH:39][CH2:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)=[N:44][C:43]2=[NH:45])[NH:5]1