Hydrochloric Acid → HCID 58641530, compound

A suspension of 6-benzenesulfonyl-4H-benzo[1,4]oxazin-3-one (1.42 g g., 4.9 mmol) in 10 ml anhydrous THF was brought to reflux, and borane-dimethyl sulfide complex (2.45 mL, 10 M in THF, 24.5 mmol) was added dropwise via syringe. The solution was refluxed for 3 hours, and the solution was cooled to room temperature and ethanolic HCl (3 mL, 2 N) was added dropwise. The resulting solution was refluxed for 1 hour and then cooled to room temperature. The reaction mixture was poured into 50 mL water, the resulting solution made basic with potassium carbonate and extracted three times with 25 mL Et2O. The organic fractions were washed with 50 mL brine, dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by flash chromatography (30 to 50% EtOAc in hexanes) to give 1.12 g of 6-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazine (83%) as a yellow solid. MS: 276 (M+H)+.

1. temperatureto reflux
2. temperatureThe solution was refluxed for 3 hours
3. temperatureThe resulting solution was refluxed for 1 hour
4. temperaturecooled to room temperature
5. extractionextracted three times with 25 mL Et2O
6. washThe organic fractions were washed with 50 mL brine
7. dry with materialdried over Na2SO4
8. concentrationconcentrated in vacuo
9. customThe resulting residue was purified by flash chromatography (30 to 50% EtOAc in hexanes)

ORD record

ord-f8a78b359cb7408c821ac485fa29f688

Source dataset

uspto-grants-2008_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07378415B2