2-methyl-N-[3-(4-piperidyl)phenyl]propanamide → N-(3-{1-[3-(1H-Indol-1-YL)propyl]-4-piperidinyl}phenyl)-2-methylpropanamide

HRID 1832995Notes

Reaction equation

HRID 1832995 reaction equation
Cl[CH2:2][CH2:3][CH2:4][N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6]1.[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]>>[N:5]1([CH2:4][CH2:3][CH2:2][N:28]2[CH2:29][CH2:30][CH:25]([C:21]3[CH:20]=[C:19]([NH:18][C:16](=[O:17])[CH:15]([CH3:14])[CH3:31])[CH:24]=[CH:23][CH:22]=3)[CH2:26][CH2:27]2)[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6]1

Participants

3

Procedure

Prepared by Procedure AH and Scheme P using 1-(3-chloropropyl)-1H-indole and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 404.2 (M+H)+.

Workup

  1. customPrepared by Procedure AH and Scheme P

Sources & evidence

ORD record
ord-b605053e624d4f4dbe6992432a899bc5
Source dataset
uspto-grants-2006_06
Patent number
US07067534B1

Reaction notes

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