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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225274생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/225274

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물3-Bromo-7-(alpha,alpha,alpha-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidineHCID 11473317—
생성물7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 2741014—

반응 단계

A mixture of 0.95 g. of 3-bromo-7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine, 0.45 g. cuprous cyanide and 25 ml. of dimethylformamide is refluxed for 16 hours. Evaporation of the reaction mixture gave a residue which was triturated with methylene chloride. The methylene chloride solution is passed through a short column of hydrous magnesium silicate. The effluent is collected and refluxed on a steam bath with gradual addition of n-hexane and the desired nitrile crystallized from solution, m.p. 141°-143° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04236005
출처 데이터셋uspto-grants-1980_11
ORD IDord-eeabe8c54d2443feb9b80e225e38510f
출처 메모uspto-grants-1980_11