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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231512생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/231512

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 (Ex. 24) in 40 ml of trifluoroacetic acid was stirred under nitrogen and heated to 60° C. in an oil bath. Then 5.0 ml of triethylsilane was added and the mixture was stirred at 60° C. for 24 hours. The reaction mixture was cooled and carefully poured into a beaker containing a 25% aqueous solution of potassium hydroxide and cracked ice. The product which precipitated was extracted into chloroform. The chloroform was washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo and gave crystals which were recrystallized from toluene-hexane to give the desired product, mp 152°-154° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847256
출처 데이터셋uspto-grants-1989_07
ORD IDord-eec79a0350064775b60e18124d16bc30
출처 메모uspto-grants-1989_07