반응 #2124938

ord-b22a6bfbaa1d458ea1582b64ff42549f

반응 방정식

CC#N.Cl
HCl CH3CN
C[C@@H](c1ccc(Br)cc1)N1CC[C@](CCC(N)=O)(c2ccc(F)cc2)OC1=O
3-((R)-3-((S)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-2-oxo-1,3-oxazinan-6-yl)propanamide
CC(C)(C)O
t-butanol
C[C@@H](c1ccc(Br)cc1)N1CC[C@](CC(C)(C)N)(c2ccc(F)cc2)OC1=O
title compound
C[C@@H](c1ccc(Br)cc1)N1CC[C@](CC(C)(C)N)(c2ccc(F)cc2)OC1=O
(S)-6-(2-amino-2-methylpropyl)-3-((S)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-1,3-oxazinan-2-one

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound was prepared from 3-((R)-3-((S)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-2-oxo-1,3-oxazinan-6-yl)propanamide following a procedure analogous to that described in Example 612 using t-butanol as solvent followed by treatment with 2 N aq HCl/CH3CN at rt. LC-MS Method 1 tR=1.41 min, m/z=449, 451 (M+1); 1H NMR (CD3OD) 7.28-7.20 (m, 4H), 7.04 (t, J=8.6 Hz, 2H), 6.96 (d, J=8.2 Hz, 2H), 5.46 (q, J=7.0 Hz, 1H), 2.99-2.94 (m, 1H), 2.34-2.28 (m, 3H), 2.16-2.07 (m, 2H), 1.43 (d, J=7.0 Hz, 3H), 1.13 (s, 3H), 0.90 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08575156B2uspto-grants-2013_11