HRID1064323

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CN(C)C=CC(=O)c1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1

HCID69665932

未命名化合物

HCID178512488

未命名化合物

PRODUCTS

生成物

结构：Clc1cccc(Nc2nccc(-c3cn(C(c4ccccc4)(c4ccccc4)c4ccccc4)cn3)n2)c1

HCID22273504

未命名化合物

PROCEDURE

实验过程

4-(3-Dimethylaminoprop-2-en-1-oyl)-1-triphenylmethylimidazole (Method 3) was treated with 3-chlorophenylguanidine under conditions analogous to those described in Example 7 to give the title compound; m/z: 514.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-189d70e2234145709c678f9459c11a27
来源数据集: uspto-grants-2005_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06969714B2
来源说明: uspto-grants-2005_11

反应 SMILES

CN(C)[CH:3]=[CH:4][C:5]([C:7]1[N:8]=[CH:9][N:10]([C:12]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:11]=1)=O.[Cl:32][C:33]1[CH:34]=[C:35]([NH:39][C:40]([NH2:42])=[NH:41])[CH:36]=[CH:37][CH:38]=1>>[Cl:32][C:33]1[CH:34]=[C:35]([CH:36]=[CH:37][CH:38]=1)[NH:39][C:40]1[N:42]=[C:5]([C:7]2[N:8]=[CH:9][N:10]([C:12]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH:11]=2)[CH:4]=[CH:3][N:41]=1