3-Nitro-4-(piperidin-1-yl)benzaldehyde → HCID 22048913, compound

HRID 1832367Notes

Reaction equation

HRID 1832367 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][C:11]=1[N:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[CH:7]=O)([O-:3])=[O:2].[CH3:18][CH:19]([CH3:35])[C:20]([NH:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]2[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]2)[CH:24]=1)=[O:21]>>[CH3:18][CH:19]([CH3:35])[C:20]([NH:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]2[CH2:34][CH2:33][N:32]([CH2:7][C:6]3[CH:9]=[CH:10][C:11]([N:12]4[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]4)=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=3)[CH2:31][CH2:30]2)[CH:24]=1)=[O:21]

Participants

3

Reactant 2

HCID 27370763-Nitro-4-(piperidin-1-yl)benzaldehydeHCID 167572552-methyl-N-[3-(4-piperidyl)phenyl]propanamide

Product 1

HCID 22048913HCID 22048913, compound

Procedure

Prepared by Procedure F and Scheme R using 3-nitro-4-(1-piperidinyl)benzaldehyde and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 465.2 (M+H)+.

Workup

  1. customPrepared by Procedure F and Scheme R

Sources & evidence

ORD record
ord-8ffe3485b312464698daa83d74866751
Source dataset
uspto-grants-2006_06
Patent number
US07067534B1

Reaction notes

Loading…