Potassium Hydroxide → (5R)-3-(5-bromo-2-pyridyloxy)-4-(4-methylsulfonylphenyl)-5-methyl-5-(2,2,2-trifluoroethyl)-5H-furan-2-one

To a 0° C. mixture of the epoxide(0.930 g) from step 1 in dimethylformamide(3 mL) and isopropanol(12 mL) was added the potassium salt of 5-bromo-2-hydroxypyridine, prepared from 5-bromo-2-hydroxypyridine and one equivalent of 8N KOH followed by evaporation to dryness with toluene and high vacuum drying, (0.742 g, 3.5 mmol) and the mixture was warmed up slowly to reflux for 16 hrs. It was then cooled to room temperature and poured on icy dilute ammonium chloride and ethyl acetate; the organic layer was separated and the aquous further extracted ounce with ethyl acetate. The combined organic layers were washed with brine, dried with MgSO4 and the solvents were removed in vacuo to yield after purification on silica gel(10% acetone/toluene) the title compound (0.380 g).

1. customfollowed by evaporation to dryness with toluene and high vacuum
2. customdrying
3. temperature(0.742 g, 3.5 mmol) and the mixture was warmed up slowly
4. temperatureto reflux for 16 hrs
5. additionpoured on icy dilute ammonium chloride and ethyl acetate
6. customthe organic layer was separated
7. washThe combined organic layers were washed with brine
8. dry with materialdried with MgSO4
9. customthe solvents were removed in vacuo
10. customto yield
11. customafter purification on silica gel(10% acetone/toluene) the title compound (0.380 g)

ORD 기록

ord-db6833f8ad4b49adbe2f05b245acd67f

출처 데이터셋

uspto-grants-1999_11

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05981576