반응 #159334

ord-df1312fadb1e463eada49a39a6f18411

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

Step 4, Method B of Example 1 was substantially repeated in this Example 4 except for employing ((R)-3-amino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl ester hydrochloride and N-Cbz-D-valine as the starting materials. Subsequent hydrogenation of the resulting benzyl ester in accordance with the procedures of Step 5, Method A of Example 1 yielded the title compound. 1H NMR (CD3OD, 300 MHz): δ 4.15-4.01 (m, 1H), 3.58 (d, 1H), 3.55-3.43 (m, 1H), 3.32-3.15 (m, 1H), 2.25-2.07 (m, 1H), 2.02-1.85 (m, 2H), 1.83-1.58 (m, 6H), 1.56-1.45 (m, 2H), 1.42-1.18 (m, 3H), 1.10 (d, 6H), 1.08-0.96 (m, 2H). 31P NMR (CD3OD, 300 MHz): δ 40.91. LCMS m/z: [M+H]+=335.1.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08828974B2uspto-grants-2014_09