(3-Chlorophenyl)hydrazine → 3-[2-(3-Chloro-phenyl)-2H-pyrazol-3-yl]-1-(4-trifluoromethanesulfonyl-phenyl)-1H-pyridazin-4-one
Reaction equation
CN(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]([C:23]([F:26])([F:25])[F:24])(=[O:22])=[O:21])=[CH:16][CH:15]=2)[N:8]=1)=O.[Cl:28][C:29]1[CH:30]=[C:31]([NH:35][NH2:36])[CH:32]=[CH:33][CH:34]=1>>[Cl:28][C:29]1[CH:30]=[C:31]([N:35]2[C:5]([C:7]3[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]4[CH:15]=[CH:16][C:17]([S:20]([C:23]([F:26])([F:24])[F:25])(=[O:22])=[O:21])=[CH:18][CH:19]=4)[N:8]=3)=[CH:4][CH:3]=[N:36]2)[CH:32]=[CH:33][CH:34]=1Participants
3
Procedure
The product was obtained starting from 3-((E)-3-Dimethylamino-acryloyl)-1-(4-trifluoromethansulfonyl-phenyl)-1H-pyridazin-4-one (A-27) and 3-chloro-phenylhydrazine according to the method described for example 1. MS: M=481.1 (M+H)+
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-e4778d69734c4cb28249fad42ed0f281
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178538B2
Reaction notes
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