1-Methylpiperazine → 2-isobutyl-4-(4-methyl-1-piperazinyl)-methyl-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one
Reaction equation
C(O[C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[C:15](=[O:33])[N:16]([CH2:29][CH:30]([CH3:32])[CH3:31])[N:17]=[C:18]([C:21]3[CH:26]=[CH:25][C:24](C)=[C:23](F)[CH:22]=3)[C:19]=2[CH3:20])[CH2:10][CH2:9]1)=O)(C)(C)C.C(N1C(=O)C(CO[S:47]([CH3:50])(=O)=O)=CC(C2C=CC(SC)=CC=2)=N1)C(C)C.CN1CCNCC1>>[CH2:29]([N:16]1[C:15](=[O:33])[C:14]([N:11]2[CH2:12][CH2:13][N:8]([CH3:6])[CH2:9][CH2:10]2)=[C:19]([CH3:20])[C:18]([C:21]2[CH:26]=[CH:25][C:24]([S:47][CH3:50])=[CH:23][CH:22]=2)=[N:17]1)[CH:30]([CH3:32])[CH3:31]Participants
4
Reactant 3
Product 1
Procedure
Following the procedure of Example 1 (10), 2-isobutyl-4-methanesulfonyloxymethyl-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one and 1-methylpiperazine were reacted to yield the title compound as a yellow oil (yield: 68.3%).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-beeed6c788104ac49612491fac170148
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07087606B2
Reaction notes
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