HRID1984185

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11009581

未命名化合物

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

HCID86261131

未命名化合物

PRODUCTS

生成物

结构：Fc1ccccc1N1CCN(CCNCc2cc(-c3ccc(C4CCCCC4)cc3)n(-c3ccccc3)n2)CC1

HCID16038997

未命名化合物

收率 64.8%

PROCEDURE

实验过程

Compound 71 was prepared using the same method as that of Example 1 except that 4-(2-fluorophenyl)piperazin-1-ylethylamine and 5-(4-cyclohexylphenyl)-1-phenyl pyrazole-3-carbaldehyde were used.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0ba99d87fd6b4512b76c72721ba2bb62
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

[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][NH2:16])[CH2:10][CH2:9]1.[CH:17]1([C:23]2[CH:28]=[CH:27][C:26]([C:29]3[N:33]([C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=4)[N:32]=[C:31]([CH:40]=O)[CH:30]=3)=[CH:25][CH:24]=2)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1>>[CH:17]1([C:23]2[CH:28]=[CH:27][C:26]([C:29]3[N:33]([C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=4)[N:32]=[C:31]([CH2:40][NH:16][CH2:15][CH2:14][N:11]4[CH2:10][CH2:9][N:8]([C:3]5[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=5[F:1])[CH2:13][CH2:12]4)[CH:30]=3)=[CH:25][CH:24]=2)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]1