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HRID 251913作成日:2026年10月23日

Water → 5-BroMo-N,N-diMethylpyrazole-1-sulfonaMide

https://huagongshe.com/ja/reaction/251913

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
反応物N,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 10954038—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5-BroMo-N,N-diMethylpyrazole-1-sulfonaMideHCID 5766099183.4%

反応条件

温度-78 °C

反応手順

To a mixture of 17.6 g of N,N-dimethyl-1H-pyrazole-1-sulfonamide and 200 ml of tetrahydrofuran was added dropwise 80 ml of a 1.3M solution of n-butyl lithium in hexane at −78° C., and the resulting mixture was stirred at −78° C. for 15 minutes. To the mixture, a solution of 35.8 g of 1,2-dibromo-1,1,2,2-tetrachloroethane in 60 ml of tetrahydrofuran was added dropwise, and the resulting mixture was stirred at −78° C. for 15 minutes. The reaction mixture was returned to room temperature, and stirred for 1 hour. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 21.3 g of 5-bromo-N,N-dimethyl-1H-pyrazole-1-sulfonamide of the formula:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07867949B2
出典データセットuspto-grants-2011_01
ORD IDord-c30c779f11f74b559e1b4eda0607c810
出典メモuspto-grants-2011_01