تفاعل #5163
ord-2a56e9a0f2494ea49832784e8b43d622
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1استخلاصextracted with ethyl acetate
- 2غسيلThe extract was washed with an aqueous solution of sodium chloride
- 3تجفيفdried over anhydrous magnesium sulfate
- 4أخرىthe solvent was removed by distillation under reduced pressure
- 5أخرىThe residue was purified by chromatography through silica gel (
- 6غسيلeluted with a 9:1 by volume mixture of ethyl acetate and methanol)
الإجراء التجريبي
1.85 ml of methanesulfonyl chloride was added, whilst ice-cooling, to a solution of 5.0 g of (2S, 4R)-1-(t-butoxycarbonyl)-2-carbamoyl-4-hydroxypyrrolidine [prepared as described in step (2) above] in 250 ml of dry tetrahydrofuran, followed by 3.31 ml of triethylamine. The mixture was then stirred at 0° to 5° C. for 1 hour, after which it was poured into an aqueous solution of sodium chloride and extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by chromatography through silica gel (eluted with a 9:1 by volume mixture of ethyl acetate and methanol) to afford 5.5 g of the title compound as colorless crystals.