HCID 21701834, compound → HCID 59370095, compound
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][CH:17]=[C:16]([O:20][C:21]([F:24])([F:23])[F:22])[CH:15]=2)[N:8]=1)=O.[NH:26]([C:28]1[CH:29]=[C:30]([S:34]([N:37]([CH3:39])[CH3:38])(=[O:36])=[O:35])[CH:31]=[CH:32][CH:33]=1)N>>[CH3:38][N:37]([CH3:39])[S:34]([C:30]1[CH:31]=[CH:32][CH:33]=[C:28]([N:26]2[C:5]([C:7]3[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]4[CH:19]=[CH:18][CH:17]=[C:16]([O:20][C:21]([F:24])([F:23])[F:22])[CH:15]=4)[N:8]=3)=[CH:4][CH:3]=[N:2]2)[CH:29]=1)(=[O:35])=[O:36]Participants
3
Procedure
The product was obtained starting from 3-((E)-3-Dimethylamino-acryloyl)-1-(3-trifluoromethoxy-phenyl)-1H-pyridazin-4-one (A-6) and 3-hydrazino-N,N-dimethyl-benzenesulfonamide according to the method described for example 91.
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-5e92671148c545ada81957be03cbe99c
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178538B2
Reaction notes
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