HRID902752

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID9880217

未命名化合物

结构：CC(C)CC(CN(CCCOC1=CC=CC(=CC(=O)O)C1)Cc1cccc(C(F)(F)F)c1Cl)c1ccccc1.Cl

HCID131726851

未命名化合物

PRODUCTS

生成物

结构：CC(C)C(CN(CCCOC1=CC=CC(=CC(=O)O)C1)Cc1cccc(C(F)(F)F)c1Cl)c1ccccc1.Cl

HCID131726852

未命名化合物

PROCEDURE

实验过程

The titled compound was prepared from 2-phenyl-3-methylbutylamine (Acta. Pharmaceutica Nordica (1992), 4(2), 105-9) in the same manner as the preparation of N-(2-Phenyl-4-methylpentyl)-N-(2-chloro-3-trifluoromethylbenzyl)-3-(3-carboxymethylenephenoxy)propylamine, hydrochloride, Example 189e-h. MS (ESI) 548 (MH+).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8cc11d307d4642eeaf79531d5d64818b
来源数据集: uspto-grants-2008_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07365085B2
来源说明: uspto-grants-2008_04

反应 SMILES

[C:1]1(C(C(C)C)CN)[CH:6]=CC=C[CH:2]=1.Cl.[C:14]1([CH:20](CC(C)C)[CH2:21][N:22]([CH2:35][CH2:36][CH2:37][O:38][C:39]2[CH2:40][C:41](=[CH:45][C:46]([OH:48])=[O:47])[CH:42]=[CH:43][CH:44]=2)[CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:33])([F:32])[F:31])[C:25]=2[Cl:34])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[ClH:34].[C:14]1([CH:20]([CH:1]([CH3:6])[CH3:2])[CH2:21][N:22]([CH2:35][CH2:36][CH2:37][O:38][C:39]2[CH2:40][C:41](=[CH:45][C:46]([OH:48])=[O:47])[CH:42]=[CH:43][CH:44]=2)[CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:32])([F:33])[F:31])[C:25]=2[Cl:34])[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1