Acetic Anhydride → HCID 22484945, compound

A mixture of N-tert-butyl-2-hydroxy-2-(4-pyridyl)ethanesulfonamide (6.62 g), acetic anhydride (13.2 ml) and pyridine (26.4 ml) was stirred at room temperature for 1.5 hr. To the reaction mixture was added 1,8-diazabicyclo[5.4.0]undec-7-ene (9.58 ml), and the mixture was stirred in an oil bath at 100° C. for 40 min. The reaction mixture was concentrated to dryness under reduced pressure. The residue was dissolved in ethyl acetate and washed with saturated brine. Th aqueous layer was extracted with ethyl acetate and organic layers were combined, dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to give (E)-N-tert-butyl-2-(4-pyridyl)ethenesulfonamide (3.91 g) as a pale-yellow solid.

1. stirringthe mixture was stirred in an oil bath at 100° C. for 40 min
2. concentrationThe reaction mixture was concentrated to dryness under reduced pressure
3. dissolutionThe residue was dissolved in ethyl acetate
4. washwashed with saturated brine
5. extractionTh aqueous layer was extracted with ethyl acetate and organic layers
6. dry with materialdried over magnesium sulfate
7. concentrationconcentrated to dryness under reduced pressure
8. customThe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1)

ORD record

ord-10302842ff1549d2b2626c5845155f73

Source dataset

uspto-grants-2003_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06573274B1