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HRID 2227260作成日:2026年10月26日
tert-Butyl Dimethylphosphonoacetate → 6-tert-Butoxycarbonylamino-3-(6-methoxy-pyridin-3-yl)-hex-2-enoic Acid tert-Butyl Ester
https://huagongshe.com/reaction/2227260
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | tert-Butyl Dimethylphosphonoacetate | HCID 4564495 | — |
| 反応物 | [4-(6-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic Acid tert-Butyl Ester | HCID 22086439 | — |
| 反応物 | Sodiumbis(trimethylsilylamide) | HCID 86599718 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 6-tert-Butoxycarbonylamino-3-(6-methoxy-pyridin-3-yl)-hex-2-enoic Acid tert-Butyl Ester | HCID 69987906 | — |
反応手順
To a stirred solution of t-butyl dimethylphosphonoacetate (6.86 g, 30.6 mmol) in tetrahydrofuran (150 mL) at −78° C. under argon was added a solution of sodium bis(trimethylsilylamide) (30.6 mL of a 1.0 M solution). After 15 min., a solution of 1-3 (3.0 g, 10.2 mmol) in tetrahydrofuran (30 mL) was added, and the reaction was warmed to ambient temperature, then heated to 40° C. for 1 h. The reaction mixture was then cooled to ambient temperature, diluted with ethyl acetate and washed with saturated aqueous sodium hydrogen carbonate, then saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The reaction mixture was filtered and concentrated at reduced pressure to give an oil that was purified by flash column chromatography (silica gel, 15 to 25% ethyl acetate/hexanes) to give 1-4 and its 2 isomer.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06413955B1 |
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| 出典データセット | uspto-grants-2002_07 |
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| ORD ID | ord-37ac060b518c4f7a8b14c5df320cc9c6 |
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| 出典メモ | uspto-grants-2002_07 |
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