5-Methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde → 2-Methyl-N-(3-{1-[(5-methyl-1-phenyl-1H-pyrazol-4-YL)methyl]-4-piperidinyl}phenyl)propanamide
Reaction equation
[CH3:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[CH:13]=O.[CH3:15][CH:16]([CH3:32])[C:17]([NH:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH:26]2[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]2)[CH:21]=1)=[O:18]>>[CH3:15][CH:16]([CH3:32])[C:17]([NH:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH:26]2[CH2:31][CH2:30][N:29]([CH2:13][C:3]3[CH:4]=[N:5][N:6]([C:7]4[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=4)[C:2]=3[CH3:1])[CH2:28][CH2:27]2)[CH:21]=1)=[O:18]Participants
3
Procedure
Prepared by Procedure F and Scheme R using 5-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 417.1 (M+H)+.
Workup
- customPrepared by Procedure F and Scheme R
Sources & evidence
- ORD record
- ord-4f79e0ed0f7e4fbe986d25074823ccff
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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