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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2050508생성일: 2026년 10월 26일

Triethylsilane → 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide

https://huagongshe.com/reaction/2050508

반응식

참여 물질

역할이름HCID투입량
반응물TriethylsilaneHCID 12052—
반응물Potassium HydroxideHCID 14797—
반응물4,5-Dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 2737093—
용매Trifluoroacetic acidHCID 6422—
생성물4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 135621397—

반응 조건

온도60 °C

반응 단계

A solution of 3.44 g of 4,5-dihydro-7-(3-trifluoromethyl)phenyl)pyrazolo(1,5-a)pyrimidine-3-carboxamide (Example 8) in 40 ml of trifluoroacetic acid is stirred under nitrogen and heated to 60° C. in an oil bath. Then 5.0 ml of triethylsilane is added and the mixture is stirred at 60° C. for 24 hours. The reaction mixture is cooled and carefully poured into a beaker containing a 25 percent aqueous solution of potassium hydroxide and cracked ice. The product which precipitates is extracted into chloroform, and the extract is washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate is evaporated in vacuo to give crystals which are then recrystallized from toluene-hexane to give the desired product, mp 152-154° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05013737
출처 데이터셋uspto-grants-1991_05
ORD IDord-e7de8176c5cc45b6b607074fc86f9053
출처 메모uspto-grants-1991_05