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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231510생성일: 2026년 10월 26일

7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile → 4,5-Dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/reaction/231510

반응식

참여 물질

역할이름HCID투입량
반응물7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 2741014—
반응물Sodium cyanoborohydrideHCID 5003444—
용매Acetic AcidHCID 176—
생성물4,5-Dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 135773307—

반응 단계

To a solution of 6.0 g of 7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (Ex. 3, U.S. Pat. No. 4,236,005) in 100 ml of glacial acetic acid, was added in portions, 3.0 g of sodium cyanoborohydride at room temperature under nitrogen. The mixture was stirred at room temperature for 2 hours. The precipitate was collected by filtration, washed with water, then dissolved in dichloromethane. The organic solution was neutralized with a saturated solution of sodium bicarbonate, then dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo and gave the desired product as a white solid. The product was recrystallized from isopropyl alcohol, mp 175°-177° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847256
출처 데이터셋uspto-grants-1989_07
ORD IDord-8031aa026700490d9a59d611704f7ea8
출처 메모uspto-grants-1989_07