تفاعل #165038

ord-7d48683d5bce425bb760a1b931bcd747

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction solution was partitioned into water and ethyl acetate
  2. 2
    غسيلThe organic layer was washed with water and saturated aqueous sodium chloride
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    أخرىthe solvent was evaporated under a reduced pressure
  5. 5
    أخرىThe residue was purified by NH silica gel column chromatography (ethyl acetate: methanol=10:1)

الإجراء التجريبي

To a solution of 2-amino-3-formylpyridine (1.00 g, 8.19 mmol) in pyridine (20 mL) was added hydroxylamine hydrochloride (854 mg, 12.3 mmol) at room temperature, which was stirred for 1 hour and 40 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate: methanol=10:1) to obtain the title compound (951 mg, 85%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08841327B2uspto-grants-2014_09