4-Methylphenylhydrazine monohydrochloride → HCID 22048984, compound
Reaction equation
[CH3:1][CH:2]([CH3:30])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][CH2:20][CH2:21][C:22](=O)[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH2:14][CH2:13]2)[CH:7]=1)=[O:4].Cl.[CH3:32][C:33]1[CH:38]=[CH:37][C:36]([NH:39]N)=[CH:35][CH:34]=1>>[CH3:1][CH:2]([CH3:30])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][CH2:20][C:21]3[C:37]4[C:36](=[CH:35][CH:34]=[C:33]([CH3:32])[CH:38]=4)[NH:39][C:22]=3[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH2:14][CH2:13]2)[CH:7]=1)=[O:4]Participants
3
Procedure
Prepared by Procedure E and Scheme M using 2-methyl-N-{3-[1-(5-oxo-5-phenylpentyl)-4-piperidinyl]phenyl}propanamide and 1-(4-methylphenyl)hydrazine hydrochloride: ESMS m/e: 494.3 (M+H)+.
Workup
- customPrepared by Procedure E and Scheme M
Sources & evidence
- ORD record
- ord-9308a041fd784942993406e523851ebc
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
Loading…