HRID1832339

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID16757255

2-methyl-N-[3-(4-piperidyl)phenyl]propanamide

C15H22N2O

HCID17608687

未命名化合物

PRODUCTS

生成物

结构：CC(C)C(=O)Nc1cccc(C2CCN(Cc3c(OCc4ccc(C#N)cc4)ccc4ccccc34)CC2)c1

HCID22049331

未命名化合物

PROCEDURE

实验过程

Prepared by Procedure F and Scheme R using 4-{[(1-formyl-2-naphthyl)oxy]methyl}benzonitrile and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 518.2 (M+H)+.

WORKUP

后处理

customPrepared by Procedure F and Scheme R

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5c2828f28e2b4e5393e694b58a0889b9
来源数据集: uspto-grants-2006_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07067534B1
来源说明: uspto-grants-2006_06

反应 SMILES

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