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HRID 1979464作成日:2026年10月26日
3-Bromocyclohexene → (3R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine
https://huagongshe.com/reaction/1979464
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Bromocyclohexene | HCID 137057 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (R)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine | HCID 12988641 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (3R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine | HCID 53946939 | 100% |
反応手順
3-Bromocyclohexene (7.06 g) and sodium bicarbonate (3.68 g) were added to a solution of (R)-(+)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (6.08 g) in anhydrous N,N-dimethylformamide (50 ml), and the mixture was stirred at 50° C. for one hour. The reaction mixture was allowed to cool, ice-water was added, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure,the residue was purified by silica gel column chromatography(ethyl acetate:n-hexane=1:3), to thereby obtain 7.84 g of the titled compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06239131B1 |
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| 出典データセット | uspto-grants-2001_05 |
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| ORD ID | ord-c75f7bbd45844e82a5bc132c9d783059 |
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| 出典メモ | uspto-grants-2001_05 |
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