[(5-Chloropentyl)sulfanyl]benzene → N-(3-{1-[5-(Phenylsulfanyl)pentyl]-4-piperidinyl}phenyl)propanamide
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][S:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[NH:14]1[CH2:19][CH2:18][CH:17]([C:20]2[CH:21]=[C:22]([NH:26][C:27](=[O:30])[CH2:28][CH3:29])[CH:23]=[CH:24][CH:25]=2)[CH2:16][CH2:15]1>>[C:8]1([S:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:14]2[CH2:19][CH2:18][CH:17]([C:20]3[CH:21]=[C:22]([NH:26][C:27](=[O:30])[CH2:28][CH3:29])[CH:23]=[CH:24][CH:25]=3)[CH2:16][CH2:15]2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1Participants
3
Procedure
Prepared by Procedure G and Scheme B1 using [(5-chloropentyl)sulfanyl]benzene and N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 411.1 (M+H)+.
Workup
- customPrepared by Procedure G and Scheme B1
Sources & evidence
- ORD record
- ord-9b77fbf8418943faa9fd6c5783e9d861
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
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