반응 #579246

ord-2ff5c94d0aae4e81aac176994ed8b25a

반응 방정식

N[C@H](CO)C(=O)O
D-serine
O=C(OCCOC(=O)C1CCCCC1)ON1C(=O)CCC1=O
(2,5-dioxoazolidinyloxycarbonyloxy)ethyl cyclohexanecarboxylate
O=C(N[C@H](CO)C(=O)O)OCCOC(=O)C1CCCCC1
title compound ( 27 )
수율 58.0%
O=C(N[C@H](CO)C(=O)O)OCCOC(=O)C1CCCCC1
(2R)-2-[(Cyclohexylcarbonyloxyethoxy)carbonylamino]-3-hydroxypropanoic Acid
수율 58.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타were reacted

실험 절차

Following the general procedure for the synthesis of acyloxyalkyl carbamates, D-serine (252 mg, 2.4 mmol) and (2,5-dioxoazolidinyloxycarbonyloxy)ethyl cyclohexanecarboxylate (626 mg, 2.0 mmol) were reacted to provide 350 mg (58% yield) of the title compound (27) as a white powder after work-up and mass-guided preparative HPLC purification. 1H NMR (CDCl3, 400 MHz): δ=6.79 (m, 1H), 6.05 (t, 1H), 5.45 (br s, 1H), 4.41 (m, 1H), 4.04 (m, 1H), 3.92 (m, 1H), 2.30 (m, 1H), 1.09-1.95 (m, 13H). MS (ESI) m/z 321.13 (M+NH4)+; 326.09 (M+Na)+; 302.06 (M−H)−.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07531572B2uspto-grants-2009_05