関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cyclopentylhydrazine hydrochloride | HCID 212349 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | (1-Methoxyphenylethylidene)malononitrile | HCID 86747657 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-cyclopentyl-3-phenylmethyl-4-cyano-5-amino-1H-pyrazole | HCID 21830924 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05294612 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-1fee0da0cdac4601a8f3a28dd2a52174 |
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| 出典メモ | uspto-grants-1994_03 |
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