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HRID 10074作成日:2026年10月23日
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3,3,3-trifluoro-N-[(+/-)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide
https://huagongshe.com/ja/reaction/10074
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 反応物 | 3,3,3-Trifluoropropionic acid | HCID 2777972 | — |
| 反応物 | (+/-)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one | HCID 21040236 | — |
| 反応物 | HCID 178418300 | HCID 178418300 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 3,3,3-trifluoro-N-[(+/-)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide | HCID 86597602 | 45% |
反応手順
(±)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one (128 mg, 1.13 mmol) was mixed with 3,3,3-trifluoropropionic acid in 2.3 mL of N,N-dimethylformamide. Hydroxybenzotriazole (17.4 mg, 0.11 mmol) was added followed by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (282 mg, 1.47 mmol). The pH of the reaction mixture was adjusted to 8.5 with triethylamine and the mixture was allowed to stir at ambient temperature for 2 hours. Water was then added and the reaction mixture was extracted with ethyl acetate. The combined organic extracts were washed with water and brine, then dried (sodium sulfate) and concentrated to give the crude product. This was purified by silica gel chromatography to afford 120 mg (45%) of 3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091380B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-0300c97a88a5417abebd157852f56576 |
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| 出典メモ | uspto-grants-2006_08 |
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