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HRID 1735395作成日:2026年10月27日
HOAc dioxane → (S)-2-[[(S)-2-(Acetoxyacetyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide
https://huagongshe.com/reaction/1735395
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | HOAc dioxane | HCID 22565020 | — |
| 反応物 | (S)-2-[[(S)-2-(Diazoacetyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide | HCID 54423239 | — |
| 生成物 | (S)-2-[[(S)-2-(Acetoxyacetyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide | HCID 15389023 | — |
反応手順
(S)-2-[[(S)-2-(Diazoacetyl)-1-pyrrolidinyl]carbonyl]-N-(phenylmethyl)-1-pyrrolidinecarboxamide (3.63 g) was dissolved in acetic acid-1,4-dioxane (1:1, 36 ml), and the mixture was heated at 100° C. for 10 minutes. The reaction mixture was concentrated, added with methylene chloride, washed with a saturated aqueous solution of sodium bicarbonate and water in order, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: chloroform-methanol) to give the title compound (1.47 g) (see Table 1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05536737 |
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| 出典データセット | uspto-grants-1996_07 |
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| ORD ID | ord-22e1f570dc3c4e3b92ba19b42c1e9362 |
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| 出典メモ | uspto-grants-1996_07 |
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