Реакция #1005961

Уравнение реакции

2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole

N-chlorosuccinimide

sodium thiosulfate

→

3-chloro-2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole

Выход 100.8%

Растворители

DMF

Условия реакции

Обработка

1. 1
   Экстракцияthe mixture was extracted with t-butyl methyl ether
2. 2
   ПромывкаThe organic layer was washed with water
3. 3
   Сушкаdried over anhydrous magnesium sulfate
4. 4
   Концентрированиеconcentrated under reduced pressure
5. 5
   ПромывкаThe resulting residue was washed with n-hexane

Методика

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).

Источник