HRID1984138

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID4742503

2-(4-phenylpiperazin-1-yl)ethanamine

C12H19N3

结构：O=Cc1cc(-c2ccc(C3CCCCC3)cc2)n(-c2ccccc2)n1

HCID86261131

未命名化合物

PRODUCTS

生成物

结构：c1ccc(N2CCN(CCNCc3cc(-c4ccc(C5CCCCC5)cc4)n(-c4ccccc4)n3)CC2)cc1

HCID16039472

未命名化合物

收率 71.2%

PROCEDURE

实验过程

Compound 12 was prepared using the same method as that of Example 1 except that 4-phenylpiperazin-1-ylethylamine and 5-(4-cyclohexylphenyl)-1-phenylpyrazole-3-carbaldehyde were used.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7d17052803404d7c9141e0af8a4bc667
来源数据集: uspto-grants-2009_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07544686B2
来源说明: uspto-grants-2009_06

反应 SMILES

[C:1]1([N:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][NH2:15])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:16]1([C:22]2[CH:27]=[CH:26][C:25]([C:28]3[N:32]([C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=4)[N:31]=[C:30]([CH:39]=O)[CH:29]=3)=[CH:24][CH:23]=2)[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[CH:16]1([C:22]2[CH:27]=[CH:26][C:25]([C:28]3[N:32]([C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=4)[N:31]=[C:30]([CH2:39][NH:15][CH2:14][CH2:13][N:10]4[CH2:9][CH2:8][N:7]([C:1]5[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=5)[CH2:12][CH2:11]4)[CH:29]=3)=[CH:24][CH:23]=2)[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]1