HRID735822

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID170235

Benzoyl chloride, 4-(hexyloxy)-

C13H17ClO2

结构：CCOC(=O)C(=O)N(Cc1ccccc1)Cc1ccc(N)cc1

HCID67187687

未命名化合物

PRODUCTS

生成物

结构：CCCCCCOc1ccc(C(=O)Nc2ccc(CN(Cc3ccccc3)C(=O)C(=O)OCC)cc2)cc1

HCID67186531

未命名化合物

收率 58%

PROCEDURE

实验过程

The same procedure as employed in the preparation of Example 15, step d but using 4-hexyloxy-benzoyl chloride and ethyl[(4-aminobenzyl)(benzyl)amino](oxo)acetate gave the title compound as a colorless oil (58%). M−(ESI): 515.2. HPLC (Condition A), Rt: 6.0 min (HPLC purity: 94.9%).

WORKUP

后处理

customThe same procedure as employed in the preparation of Example 15, step d

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e526092712d24841b39530a47b3d5632
来源数据集: uspto-grants-2009_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07592477B2
来源说明: uspto-grants-2009_09

反应 SMILES

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