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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1736555생성일: 2026년 10월 27일

Cyclopentylhydrazine hydrochloride → 1-cyclopentyl-3-phenylmethyl-4-cyano-5-amino-1H-pyrazole

https://huagongshe.com/reaction/1736555

반응식

참여 물질

역할이름HCID투입량
반응물Cyclopentylhydrazine hydrochlorideHCID 212349—
반응물Sodium MethoxideHCID 10942334—
반응물(1-Methoxyphenylethylidene)malononitrileHCID 86747657—
용매EthanolHCID 702—
생성물1-cyclopentyl-3-phenylmethyl-4-cyano-5-amino-1H-pyrazoleHCID 2183092426%

반응 단계

A mixture of cyclopentyl hydrazine hydrochloride (1.4 g, 10.2 mmol), sodium methoxide (0.55 g, 10.2 mmol) and ethanol (30 ml) was heated to reflux and then (1-methoxyphenylethylidene)malononitrile (2.0 g, 10.2 mmol) in ethanol (15 ml) was added dropwise over 1 hour. The reaction mixture was refluxed for 6.5 hours and the solvent was removed in vacuo. The residue was partitioned between chloroform and water, the organic layer was separated and the aqueous layer was extracted with chloroform (3×75 ml). The combined organic layers were washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo to afford 0.7 g (26%) of 1-cyclopentyl-3-phenylmethyl-5-amino-1H-pyrazole-4-carbonitrile as white flakes, m.p. 180°-182° C. when recrystallized from ethyl acetate and dried for 18 hours at 90° C. in high vacuum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05541187
출처 데이터셋uspto-grants-1996_07
ORD IDord-162bb1cec3ac403caa1b9a7b7b3b9023
출처 메모uspto-grants-1996_07