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HRID 246867作成日:2026年10月26日
Ammonia → 3-Amino-3[2-(4-ethyl-2,3-dioxopiperazine-1-carbonylamino)-2-phenylacetamido]-4-methylazetidin-2-one
https://huagongshe.com/reaction/246867
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | 3[2-(4-Ethyl-2,3-dioxopiperazine-1-carbonylamino)-2-phenylacetamido]-4-methyl-3-methylsulphinylazetidin-2-one | HCID 20162853 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 3-Amino-3[2-(4-ethyl-2,3-dioxopiperazine-1-carbonylamino)-2-phenylacetamido]-4-methylazetidin-2-one | HCID 20162861 | — |
反応手順
The sulphoxide (61) (145 mg) in dioxan (5 ml) was treated with ammonia (21 ml) overnight at room temperature. The solvent was then evaporated and the residue chromatographed on silica gel to give the product (62) as a white solid (95 mg), νmax. (CHCl3) 3400, 3280, 1770, 1715 and 1690 cm-1, δ(CDCl3) 0.87, 0.90, 1.10 and 1.14 (each d, J 6 Hz, together 3H), 1.20 (t, J 7Hz, 3H), 1.6-2.9 br (2H, exch.), 3.40-3.65 (m, 4H) (irradiation at 0.90 caused this signal to simplify), 3.85 (2×q, J 7 Hz, together 1H) (irradiation at 0.87 or 1.10 caused one of the above signals to collapse to a s), 3.95-4.13 (m, 2H), 5.45 (2×d, J 7 Hz, together 1H, collapses to 2×s on exch), 6.50, 6.58, 6.63, and 6.72 br (each s, together 1H, exch.), 7.25-7.56 (m, 5H), 7.62, 7.76, 7.90, and 8.06 br (each s, 1H, exch.), and 9.90 (2×d, J7 Hz, together 1H, exch.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04704385 |
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| 出典データセット | uspto-grants-1987_11 |
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| ORD ID | ord-cae88bd7706243cd82806faab99d8c6a |
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| 出典メモ | uspto-grants-1987_11 |
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