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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1587787생성일: 2026년 10월 25일

Sodium cyanoborohydride → N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide

https://huagongshe.com/reaction/1587787

반응식

참여 물질

역할이름HCID투입량
반응물Sodium cyanoborohydrideHCID 5003444—
반응물N-DesesethylzaleplonHCID 9993635—
반응물N-[3-(3-Dimethylaminoacryloyl)phenyl]acetamideHCID 53412415—
반응물HCID 178510443HCID 178510443—
용매Acetic AcidHCID 176—
생성물N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamideHCID 136093204—

반응 단계

A mixture of 7.0 g of 3'-actamido-3-(N,N-dimethylamino)acrylophenone and 3.3 g. of 3-amino-4-cyanopyrazole in 100 ml of acetic acid was heated at reflux for 8 hours. Crystals that formed on cooling were filtered and dried to give 7.4 g. of N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide, m.p. 254°-256° C. This was reacted with 14.8 g of sodium cyanoborohydride in 50 ml of acetic acid to give 3.0 g of N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]-pyrimidin-7-yl)phenyl]acetamide, m.p. 251°-254° C. This is reacted with chloroacetic anhydride and sodium carbonate in toluene as in Example 3 to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05219857
출처 데이터셋uspto-grants-1993_06
ORD IDord-8b34082632574383ad196a4a83b014b4
출처 메모uspto-grants-1993_06