2-methyl-N-[3-(4-piperidyl)phenyl]propanamide → N-(3-{1-[(2S)-3-(2-Chlorophenoxy)-2-methylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide

HRID 1832560Notes

Reaction equation

HRID 1832560 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH2:9][C@@H:10]([CH3:13])[CH2:11]Cl.[CH3:14][CH:15]([CH3:31])[C:16]([NH:18][C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH:25]2[CH2:30][CH2:29][NH:28][CH2:27][CH2:26]2)[CH:20]=1)=[O:17]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH2:9][C@@H:10]([CH3:13])[CH2:11][N:28]1[CH2:29][CH2:30][CH:25]([C:21]2[CH:20]=[C:19]([NH:18][C:16](=[O:17])[CH:15]([CH3:14])[CH3:31])[CH:24]=[CH:23][CH:22]=2)[CH2:26][CH2:27]1

Participants

3

Reactant 2

HCID 167572552-methyl-N-[3-(4-piperidyl)phenyl]propanamideHCID 695239811-Chloro-2-{[(2R)-3-chloro-2-methylpropyl]oxy}benzene

Product 1

HCID 58651325N-(3-{1-[(2S)-3-(2-Chlorophenoxy)-2-methylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide

Procedure

Prepared by Procedure G and Scheme B1 using 1-chloro-2-{[(2R)-3-chloro-2-methylpropyl]oxy}benzene and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 429.1 (M+H)+.

Workup

  1. customPrepared by Procedure G and Scheme B1

Sources & evidence

ORD record
ord-10c4248c20584455b7ba2641c0e70953
Source dataset
uspto-grants-2006_06
Patent number
US07067534B1

Reaction notes

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