N-Methylmethanesulfonamide → HCID 24826096, compound
Reaction equation
Cl[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:17]3[CH2:16][CH2:15][CH2:14][CH2:13][C:12]=3[C:11]([C:18]([F:21])([F:20])[F:19])=[N:10]2)=[CH:5][CH:4]=1.[CH3:22][NH:23][S:24]([CH3:27])(=[O:26])=[O:25]>>[CH3:22][N:23]([CH2:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:17]3[CH2:16][CH2:15][CH2:14][CH2:13][C:12]=3[C:11]([C:18]([F:21])([F:20])[F:19])=[N:10]2)=[CH:5][CH:4]=1)[S:24]([CH3:27])(=[O:26])=[O:25]Participants
3
Procedure
The title compound was prepared from 1-[4-(chloromethyl)phenyl]-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole and N-methyl methanesulfonamide using a similar procedure to that described for Description 15.
Sources & evidence
- ORD record
- ord-fb38df4955f344da921ae80d75be164a
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07566735B2
Reaction notes
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