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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

反応式

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-lysineHCID 86762028—
溶媒Ethyl AcetateHCID 8857—
溶媒piperidine N,N-dimethylformamideHCID 23501187—
生成物Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysineHCID 8676202785.6%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524691B2
出典データセットuspto-grants-2013_09
ORD IDord-9ace8feb681144c797b9b24e1829a87f
出典メモuspto-grants-2013_09