HRID1984200

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID14210620

未命名化合物

HCID86611059

未命名化合物

PRODUCTS

生成物

结构：Cc1ccc(-c2cc(CNCCN3CCN(C(c4ccccc4)c4ccc(Cl)cc4)CC3)nn2C(C)(C)C)cc1

HCID68974445

未命名化合物

收率 41%

PROCEDURE

实验过程

Compound 99 was prepared using the same method as that of Example 1 except for using 4-(4-chlorobenzhydryl)piperazin-1-ylethylamine and 1-t-butyl-5-(4-methylphenyl)pyrazole-3-carbaldehyde.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-78deba9c59ee46f4a23af285d616507d
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

[Cl:1][C:2]1[CH:23]=[CH:22][C:5]([CH:6]([N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][NH2:21])[CH2:15][CH2:14]2)[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.[C:24]([N:28]1[C:32]([C:33]2[CH:38]=[CH:37][C:36]([CH3:39])=[CH:35][CH:34]=2)=[CH:31][C:30]([CH:40]=O)=[N:29]1)([CH3:27])([CH3:26])[CH3:25]>>[C:24]([N:28]1[C:32]([C:33]2[CH:34]=[CH:35][C:36]([CH3:39])=[CH:37][CH:38]=2)=[CH:31][C:30]([CH2:40][NH:21][CH2:20][CH2:19][N:16]2[CH2:15][CH2:14][N:13]([CH:6]([C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:5]3[CH:4]=[CH:3][C:2]([Cl:1])=[CH:23][CH:22]=3)[CH2:18][CH2:17]2)=[N:29]1)([CH3:27])([CH3:26])[CH3:25]