1-Isocyanato-2-(methylsulfanyl)benzene → 2-Methyl-N-(3-{1-[3-({[2-(methylsulfanyl)anilino]carbonyl}amino)propyl]-4-piperidinyl}phenyl)propanamide
Reaction equation
[N:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][CH3:11])=[C:2]=[O:3].[NH2:12][CH2:13][CH2:14][CH2:15][N:16]1[CH2:21][CH2:20][CH:19]([C:22]2[CH:23]=[C:24]([NH:28][C:29](=[O:33])[CH:30]([CH3:32])[CH3:31])[CH:25]=[CH:26][CH:27]=2)[CH2:18][CH2:17]1>>[CH3:31][CH:30]([CH3:32])[C:29]([NH:28][C:24]1[CH:25]=[CH:26][CH:27]=[C:22]([CH:19]2[CH2:18][CH2:17][N:16]([CH2:15][CH2:14][CH2:13][NH:12][C:2]([NH:1][C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[S:10][CH3:11])=[O:3])[CH2:21][CH2:20]2)[CH:23]=1)=[O:33]Participants
3
Procedure
Prepared by Procedure P and Scheme AB using 1-isocyanato-2-(methylsulfanyl)benzene and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}-2-methylpropanamide: ESMS m/e: 469.1 (M+H)+.
Workup
- customPrepared by Procedure P and Scheme AB
Sources & evidence
- ORD record
- ord-f715004be085429c9dc2c24c446471e9
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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