Reaction #1005961
ord-3888f7a4df22403fadecfbef95e3f411
Reaction equation
2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole
N-chlorosuccinimide
sodium thiosulfate
→
3-chloro-2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole
Yield 100.8%
Reactants
Reagents
None
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1Extractionthe mixture was extracted with t-butyl methyl ether
- 2WashThe organic layer was washed with water
- 3Dryingdried over anhydrous magnesium sulfate
- 4Concentrationconcentrated under reduced pressure
- 5WashThe resulting residue was washed with n-hexane
Procedure
A mixture of 226 mg of 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole, 86 mg of N-chlorosuccinimide and 2 ml of DMF was stirred at room temperature for 10 hours. A 10% aqueous sodium thiosulfate solution was poured to the reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, then concentrated under reduced pressure. The resulting residue was washed with n-hexane to obtain 250 mg of 3-chloro-2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole (hereinafter, referred to as Compound of Present Invention 3).