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HRID 487264作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclopentylhydrazine hydrochlorideHCID 212349—
反応物Sodium MethoxideHCID 10942334—
反応物(1-Methoxyphenylethylidene)malononitrileHCID 86747657—
溶媒EthanolHCID 702—
生成物1-cyclopentyl-3-phenylmethyl-4-cyano-5-amino-1H-pyrazoleHCID 2183092426%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05294612
出典データセットuspto-grants-1994_03
ORD IDord-1fee0da0cdac4601a8f3a28dd2a52174
出典メモuspto-grants-1994_03