돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487264생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/487264

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 번호US05294612
출처 데이터셋uspto-grants-1994_03
ORD IDord-1fee0da0cdac4601a8f3a28dd2a52174
출처 메모uspto-grants-1994_03