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HRID 39270作成日:2026年10月23日
Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine → Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine
https://huagongshe.com/ja/reaction/39270
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine | HCID 86762028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | piperidine N,N-dimethylformamide | HCID 23501187 | — |
| 生成物 | Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine | HCID 86762027 | 85.6% |
反応手順
A solution of 90 (502 mg, 0.616 mmol) in piperidine/DMF (0.05:1, 5 mL) was stirred at room temperature for 18 hr. After diluting with ethyl acetate (40 mL) the organic layer was washed with water and brine then dried over Na2SO4 and concentrated in vacuo. The crude material was purified by silica gel chromatography (methanol in ethyl acetate, 5% over 5 column volumes then 5 to 30% over 10 column volumes) using a Biotage Horizon™ apparatus resulting in the colourless liquid 91 (249 mg, 68%): 1H NMR (400 MHz, CDCl3) δ 1.39-1.74 (m, 6H), 1.45 (s, 9H), 2.21-2.35 (m, 2H), 2.51 (t, J=7.4, 2H), 2.55 (tt, J=6.9, 23.9, 1H), 3.19-3.25 (m, 2H), 3.29 (dd, J=5.2, 7.6, 1H), 4.58-4.63 (m, 8H), 5.25 (dq, J=1.3, 10.3, 4H), 5.38 (dq, J=1.4, 17.1, 4H), 5.90-6.00 (m, 4H), 6.14 (bd, J=4.9, 1H): 31P (162 MHz, CDCl3) δ 24.67 (s, 2P).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524691B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-9ace8feb681144c797b9b24e1829a87f |
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| 出典メモ | uspto-grants-2013_09 |
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