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HRID 39270Erstellt: 23. Oktober 2026

Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine → Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine

https://huagongshe.com/de/reaction/39270

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysineHCID 86762028—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittelpiperidine N,N-dimethylformamideHCID 23501187—
ProduktNepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysineHCID 8676202785,6%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524691B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-9ace8feb681144c797b9b24e1829a87f
Quellennotizuspto-grants-2013_09