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HRID 12873作成日:2026年10月24日
tert-Butylhydrazine monohydrochloride → 1-tert-butyl-5-(5-methyl-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid methyl ester
https://huagongshe.com/ja/reaction/12873
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 3-Dimethylamino-2-(5-methyl-isoxazole-3-carbonyl)-acrylic acid ethyl ester | HCID 67020947 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-tert-butyl-5-(5-methyl-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid methyl ester | HCID 67021103 | 101.7% |
反応手順
A solution of 3-dimethylamino-2-(5-methyl-isoxazole-3-carbonyl)-acrylic acid ethyl ester (27.53 mmol) in absolute ethanol (41.7 mL) was treated with tert-butylhydrazine hydrochloride (3.57 g, 28.63 mmol) and sodium acetate (2.80 g, 34.13 mmol). The resulting mixture was heated to 90° C. for 18 h. At this time, the reaction was cooled to 25° C. The reaction was diluted with water (200 mL) and was then extracted with dichloromethane (3×150 mL). The combined organics were dried over sodium sulfate, filtered and concentrated in vacuo to afford 1-tert-butyl-5-(5-methyl-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid methyl ester (7.37 g, 96%) as a black solid. The material was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728029B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-992fdccc9f344eb986ca721d7e723ab4 |
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| 出典メモ | uspto-grants-2010_06 |
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