HRID379449

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID15723

Azacyclonol

C18H21NO

结构：CN(CC(CCS(C)(=O)=O)c1ccccc1)C(=O)c1ccccc1

HCID18354437

未命名化合物

PRODUCTS

生成物

结构：CN(CC(CCN1CCC(C(O)(c2ccccc2)c2ccccc2)CC1)c1ccccc1)C(=O)c1ccccc1

HCID15870532

未命名化合物

PROCEDURE

实验过程

Prepare by the method of Example 1.7 using N-methyl-N-(2-phenyl-4-methanesulfonylbutyl)benzamide and 4-(hydroxydiphenylmethyl)piperidine to give the title compound.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-1b2bab0e5f8145279edc6d62e10d48ef
来源数据集: uspto-grants-2001_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06297259B1
来源说明: uspto-grants-2001_10

反应 SMILES

[CH3:1][N:2]([CH2:11][CH:12]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH2:13][CH2:14]S(C)(=O)=O)[C:3](=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[OH:25][C:26]([C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[CH:27]1[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]1>>[CH3:1][N:2]([CH2:11][CH:12]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH2:13][CH2:14][N:30]1[CH2:31][CH2:32][CH:27]([C:26]([OH:25])([C:33]2[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=2)[C:39]2[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=2)[CH2:28][CH2:29]1)[C:3](=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1