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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1069생성일: 2026년 10월 23일

Pyrazole → 4,4,5,8-Tetramethyl-6-(1-ethyl-5-ethanesulfonyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide

https://huagongshe.com/ko/reaction/1069

반응식

참여 물질

역할이름HCID투입량
반응물PyrazoleHCID 1048—
반응물Potassium CarbonateHCID 11430—
반응물Ethanesulfonyl chlorideHCID 11667—
반응물HCID 178418286HCID 178418286—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4,4,5,8-Tetramethyl-6-(1-ethyl-5-ethanesulfonyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxideHCID 1547735882%

반응 단계

0.7 Gram (1.9 mmol) of the 4,4,5,8-tetramethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound Ic-1) corresponding to pyrazole derivative (I-H), obtained in Referential Production Example 5, was dissolved in 8 ml of methylene chloride. Then, a solution of 0.51 g (3.8 mmol) of potassium carbonate in 5 ml of water was added, and further, 0.49 g (3.8 mmol) of ethanesulfonyl chloride and 0.05 g (0.2 mmol) of benzyltriethylammonium chloride, corresponding to compound B-A-Hal, were added. The mixture was allowed to react at room temperature for 2 hours, and further refluxed under heat for 2 hours. The reaction mixture was allowed to cool, and then a methylene chloride layer was recovered and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resultant oil was purified by silica gel column chromatography to give 0.73 g (yield 82%) of 4,4,5,8-tetramethyl-6-(1-ethyl-5-ethanesulfonyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound Ic-2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723408
출처 데이터셋uspto-grants-1998_03
ORD IDord-b437e05b173c435b946ece88305eb18d
출처 메모uspto-grants-1998_03