4-(3,4-Difluorophenoxy)benzaldehyde → N-(5-{1-[4-(3,4-Difluorophenoxy)benzyl]-4-piperidinyl}-2-methylphenyl)-2-methylpropanamide
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][C:16]=1[F:17])[O:5][C:6]1[CH:13]=[CH:12][C:9]([CH:10]=O)=[CH:8][CH:7]=1.[CH3:18][CH:19]([CH3:36])[C:20]([NH:22][C:23]1[CH:28]=[C:27]([CH:29]2[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]2)[CH:26]=[CH:25][C:24]=1[CH3:35])=[O:21]>>[F:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][C:16]=1[F:17])[O:5][C:6]1[CH:13]=[CH:12][C:9]([CH2:10][N:32]2[CH2:33][CH2:34][CH:29]([C:27]3[CH:26]=[CH:25][C:24]([CH3:35])=[C:23]([NH:22][C:20](=[O:21])[CH:19]([CH3:18])[CH3:36])[CH:28]=3)[CH2:30][CH2:31]2)=[CH:8][CH:7]=1Participants
3
Procedure
Prepared by Procedure AA and Scheme AJ using 4-(3,4-difluorophenoxy)benzaldehyde and 2-methyl-N-[2-methyl-5-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 479.2 (M+H)+.
Workup
- customPrepared by Procedure AA and Scheme AJ
Sources & evidence
- ORD record
- ord-72a3fde3668f4659bd2a514b4a256414
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
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