反应详情

A solution of 2,2-dimethyl-3-((R)-2-oxo-3-((S)-1-(4-(6-oxo-1,6-dihydropyridin-3-yl)phenyl)ethyl)-6-phenyl-1,3-oxazinan-6-yl)propanenitrile (202 mg, 0.444 mmol) and MeI (110 μL, 4 equiv) in dry THF (5 mL) was cooled to 0° C. NaH (60% in mineral oil, 36 mg, 2 equiv) was added. After 10 min, the mixture was warmed to rt slowly and stirred for 3 h. LC-MS showed about 50% conversion. The mixture was heated for 1 h at 60° C. LC-MS found the reaction completed. After cooling to rt, the mixture was cooled to 0° C. and quenched with satd aq NH4Cl (3 mL). The mixture was then diluted with CH2Cl2 (20 mL), washed with 1% aq HCl (5 mL) and brine (4 mL), and dried over Na2SO4. After filtration and concentration, the residue was purified by prep HPLC to afford 2,2-dimethyl-3-((R)-3-((S)-1-(4-(1-methyl-6-oxo-1,6-dihydropyridin-3-yl)phenyl)ethyl)-2-oxo-6-phenyl-1,3-oxazinan-6-yl)propanenitrile (177.4 mg, 85% yield) product as a light brown oil.

1. temperatureThe mixture was heated for 1 h at 60° C
2. temperatureAfter cooling to rt
3. temperaturethe mixture was cooled to 0° C.
4. customquenched with satd aq NH4Cl (3 mL)
5. additionThe mixture was then diluted with CH2Cl2 (20 mL)
6. washwashed with 1% aq HCl (5 mL) and brine (4 mL)
7. dry with materialdried over Na2SO4
8. filtrationAfter filtration and concentration
9. customthe residue was purified by prep HPLC