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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclopentylhydrazine hydrochloride | HCID 212349 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | (1-Methoxyphenylethylidene)malononitrile | HCID 86747657 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-cyclopentyl-3-phenylmethyl-4-cyano-5-amino-1H-pyrazole | HCID 21830924 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05541187 |
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| 출처 데이터셋 | uspto-grants-1996_07 |
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| ORD ID | ord-162bb1cec3ac403caa1b9a7b7b3b9023 |
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| 출처 메모 | uspto-grants-1996_07 |
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