Реакция #49888

Уравнение реакции

methyl disulfide

butyllithium

4-chloro-1-(diethylcarbamoyl)-3-(2-ethyl-6-methylphenylsulfonyl)pyrazole

ammonium chloride

→

title compound

Выход 35.0%

4-Chloro-1-(diethylcarbamoyl)-3-(2-ethyl-6-methylphenylsulfonyl)-5-methylthiopyrazole

Выход 35.0%

Растворители

hexane

tetrahydrofuran

Условия реакции

Обработка

1. 1
   ДругоеThe resulting reaction mixture
2. 2
   workup.STIRRINGwas stirred for 30 minutes
3. 3
   Экстракцияextracted with diethyl ether
4. 4
   ПромывкаThe extract was washed with water
5. 5
   Сушкаdried over anhydrous sodium sulfate
6. 6
   Концентрированиеconcentrated by evaporation under reduced pressure
7. 7
   ДругоеThe concentrate was purified by column chromatography through silica gel
8. 8
   Промывкаeluted with a 10:1 by volume mixture of hexane and ethyl acetate

Методика

0.11 ml of a 1.49M solution of butyllithium in hexane was added, at -78° C. and under an atmosphere of nitrogen, to a solution of 59 mg of 4-chloro-1-(diethylcarbamoyl)-3-(2-ethyl-6-methylphenylsulfonyl)pyrazole (prepared as described in Example 18) in 2 ml of dry tetrahydrofuran, and the resulting mixture was stirred for 30 minutes, after which 15 μl of methyl disulfide were added. The resulting reaction mixture was stirred for 30 minutes, and then mixed with an aqueous solution of ammonium chloride and extracted with diethyl ether. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, eluted with a 10:1 by volume mixture of hexane and ethyl acetate, to afford 28 mg (yield 35%) of the title compound as an oil.

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