Sulfur Dioxide → 5-Methyl-2-pyridinesulfonamide

Sec-butyllithium (9.8 ml of 1.3M in cyclohexane) and N,N,N′,N′-tetramethylethylenediamine (1.8 ml, 12.2 mmol) were added to a stirred solution of 2-bromo-5-methylpyridine (2 g, 11.6 mmol) at −78° C. under a nitrogen atmosphere. After 90 min sulphur dioxide (approximately 30 ml) was condensed into the reaction mixture using a cold finger and the reaction mixture was slowly warmed to room temperature over 12 h. The reaction mixture was concentrated to dryness and the residue dissolved in ice-water. To this was added a mixture of sodium hydroxide (1.39 g, 35 mmol) and hydroxylamine sulphonic acid (3.9 g, 35 mmol) in water (20 ml). After 24 h the solution was extracted with ethyl acetate, dried (MgSO4) and concentrated. Flash column chromatography (95% dichloromethane /5% methanol) gave the product (250 mg) as a clear oil which crystallised on standing.

1. customcondensed into the reaction mixture
2. concentrationThe reaction mixture was concentrated to dryness
3. dissolutionthe residue dissolved in ice-water
4. additionTo this was added
5. extractionAfter 24 h the solution was extracted with ethyl acetate
6. dry with materialdried (MgSO4)
7. concentrationconcentrated

ORD record

ord-08bc1367155840a8859371acab70bd4b

Source dataset

uspto-grants-2001_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06306852B1