تفاعل #2568
ord-4df58d28e9e34965aa240b18daf00714
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىethanol was removed by evaporation
- 2workup.ADDITIONthe resulting residue was mixed with water (10 ml)
- 3أخرىto collect crystals
- 4ترشيحby filtration
- 5غسيلThe thus collected crystals were washed with water and hexane
- 6workup.DISSOLUTIONdissolved in methylene chloride (50 ml)
- 7تجفيفdried on anhydrous sodium carbonate
- 8أخرىThereafter, the solvent was removed by evaporation
الإجراء التجريبي
N-{2-[4-(4-Fluorobenzoyl)piperidino]ethyl}-4-formyl-N-(2-methoxyphenyl)benzenesulfonamide (63 mg, 0.12 mmol) and hydroxyamine hydrochloride (9.5 mg, 0.132 mmol) were dissolved in ethanol (2 ml) to which were subsequently added anhydrous sodium carbonate (14 mg, 0.132 mmol) and water (1 ml). After 1.5 hours of stirring at room temperature, ethanol was removed by evaporation, and the resulting residue was mixed with water (10 ml) to collect crystals by filtration. The thus collected crystals were washed with water and hexane, dissolved in methylene chloride (50 ml) and then dried on anhydrous sodium carbonate. Thereafter, the solvent was removed by evaporation to obtain 65 mg (100%) of the title compound in the form of colorless powder.