反应详情

The title compound was prepared as described in Example B(53), using 2-[5-(chloromethyl)-1,2,4-oxadiazol-3-yl]pyridine (from Step 1, below) in place of 5-(chloromethyl)-1,3-dimethyl-1H-1,2,4-triazole, and using 6-[2-(5-chloro-2,4-dimethoxyphenyl)ethyl]-6-cyclopentyldihydro-2H-pyran-2,4(3H)-dione in place of 6-[2-(3-chloro-4-methoxyphenyl)ethyl]-6-cyclopentyldihydro-2H-pyran-2,4(3H)-dione. Yield: 9%. 1H NMR (300 MHz, DMSO-d6) δ 1.25-1.75 (m, 8H), 1.76-2.03 (m, 2H), 2.34 (m, 1H), 2.4-2.55 (m, 2H, overlap with DMSO-d5), 2.62 (d, J=17.7 Hz, 1H), 2.81 (d, J=17.7 Hz, 1H), 3.74 (s, 3H, overlap with H2O), 3.80 (s, 3H), 3.90 (ABQ pattern, J=16.8 Hz, 2H), 6.66 (s, 1H), 7.13 (s, 1H), 7.55 (m, 1H), 7.81 (m, 2H), 8.70 (d, J=4.8 Hz, 1H), 11.43 (br s, 1H). LC-MS (APCI) calcd for C28H30ClN3O6: 539.18; found (M+H+): 540.1 m/z.