Methanol → HCID 86749413, compound

Participants

Reaction Steps

A solution of (E)-7-[2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinyl]-5-hydroxy-3-oxo-6-heptenoic acid, methyl ester (182 mg, 0.39 mmol) in THF (5.5 ml) was treated with triethylborane (1.0N in THF, 830 ul, 0.83 mmol). Twenty milliliters of air was bubbled through the solution and the mixture was stirred at room temperature for 30 minutes. The solution was cooled to -78° C. and treated with NaBH4 (15.0 mg, 0.40 mmol) followed by dropwise addition of dry methanol (0.9 ml). After stirring at -78° C. for 1.75 hours, the mixture was quenched with 30% H2 O2 (2.8 ml) in H2O (6 ml). The mixture was kept at -78° C. for 15 minutes, then warmed to room temperature and stirred for 45 minutes. The solution was poured into 50% saturated NaHCO3 and extracted with Et2O (2×). The combined Et2O extracts were washed with saturated NaHCO3, H2O, and brine, then dried (Na2SO4), filtered and stripped. Purification of the resulting oil (flash, Merck SiO2, 50% EtOAc in hexane) gave (3R*, 5S*, 6E)-7-[2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinyl]-3,5-dihydroxy-6-heptenoic acid, methyl ester (157 mg, 86%) as a colorless oily foam.

Provenance & Evidence