関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Penten-1-OL | HCID 13181 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Triphosgene | HCID 94429 | — |
| 反応物 | L-tert-Leucine | HCID 164608 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 3-Methyl-N-{[(pent-4-en-1-yl)oxy]carbonyl}-L-valine | HCID 45379928 | 147.8% |
反応手順
A solution of 4-pentenol (7.22 g, 83.8 mmol) and triphosgene (11.3 g, 38.1 mmol) in dioxane (160 mL) was cooled to 0° C. followed by a dropwise addition of DIPEA (9.85 g, 76.2 mL). The white suspension was stirred vigorously for 1 h at 25° C., then cooled to 0° C. A 1 N solution of NaOH (76.2 mL) and t-butylglycine (10.0 g, 76.2 mmol) were added. The resulting suspension was warmed to 25° C. and stirred for 18 h. Approximately half of the dioxane was removed in vacuo, the solution was poured into 1 N NaOH (100 mL) and washed with dichloromethane (3×150 mL). The aqueous layer was acidified with 6 N HCl and the desired product was extracted with dichloromethane (3×150 mL). The combined organics were dried over MgSO4 and concentrated to give 13.7 g (73.9% yield) of 3-methyl-N-[(pent-4-enyloxy)carbonyl]-L-valine as a colorless oil. LRMS (ESI) m/z 244 [(M+H)+; calcd for C12H22NO4: 244].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08216999B2 |
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| 出典データセット | uspto-grants-2012_07 |
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| ORD ID | ord-ace76892f46a483e995b6f053aaf366e |
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| 出典メモ | uspto-grants-2012_07 |
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