Aluminium lithium hydride → HCID 58109290, compound

Participants

Reaction Conditions

Reaction Steps

Methyl 4-((S)-1-((R)-6-(4-fluorophenyl)-6-(3-hydroxypropyl)-2-oxo-1,3-oxazinan-3-yl)ethyl)benzoate (10 mg, 0.024 mmol) was dissolved in dry THF (4 mL) and cooled to 0° C. LiAlH4 (2 mg, excess) was added slowly. After 10 min, the mixture was warmed to rt and stirred for 2 h. LC-MS found reaction completed. The mixture was quenched with water, diluted with EtOAc (5 mL), washed with 1% aq HCl (2 mL). After concentration, the residue was purified by prep HPLC to afford (R)-6-(4-fluorophenyl)-3-((S)-1-(4-(hydroxymethyl)phenyl)ethyl)-6-(3-hydroxypropyl)-1,3-oxazinan-2-one (3.0 mg, 32%). LC-MS Method 1 tR=1.2 min, m/z=410 (M+Na); 1H NMR (CDCl3) 7.23 (m, 2H), 7.14 (d, 2H), 7.03 (q, 2H), 6.95 (t, 2H), 5.66 (m, 1H), 4.61 (s, 2H), 3.59 (t, 2H), 1.53 (d, 3H).

Provenance & Evidence