5-Hydrazinylisoquinoline → 3-(2-Isoquinolin-5-yl-2H-pyrazol-3-yl)-1-(4-methanesulfonyl-phenyl)-1H-pyridazin-4-one
Reaction equation
C[N:2](C)/[CH:3]=[CH:4]/[C:5]([C:7]1[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]2[CH:19]=[CH:18][C:17]([S:20]([CH3:23])(=[O:22])=[O:21])=[CH:16][CH:15]=2)[N:8]=1)=O.[CH:25]1[C:34]2[C:29](=[C:30]([NH:35]N)[CH:31]=[CH:32][CH:33]=2)[CH:28]=[CH:27][N:26]=1>>[CH:25]1[C:34]2[C:29](=[C:30]([N:35]3[C:5]([C:7]4[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]5[CH:19]=[CH:18][C:17]([S:20]([CH3:23])(=[O:22])=[O:21])=[CH:16][CH:15]=5)[N:8]=4)=[CH:4][CH:3]=[N:2]3)[CH:31]=[CH:32][CH:33]=2)[CH:28]=[CH:27][N:26]=1Participants
3
Procedure
The product was obtained starting from 3-((E)-3-Dimethylamino-acryloyl)-1-(4-methansulfonyl-phenyl)-1H-pyridazin-4-one (A-16) and isoquinolin-5-yl-hydrazine according to the method described for example 43. MS: M=444.5 (M+H)+
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-98a3b83a53d643fa9927c2093746063f
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178538B2
Reaction notes
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