تفاعل #5168

ord-2785b6e61574455283939136e0ff5801

معادلة التفاعل

[Cl-].[Na+]
sodium chloride
CCN(CC)CC
triethylamine
CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
(2S, 4R)-1-(t-butoxycarbonyl)-2-methylcarbamoyl-4-hydroxypyrrolidine
CS(=O)(=O)Cl
methanesulfonyl chloride
CNC(=O)[C@@H]1C[C@@H](OS(C)(=O)=O)CN1C(=O)OC(C)(C)C
title compound
CNC(=O)[C@@H]1C[C@@H](OS(C)(=O)=O)CN1C(=O)OC(C)(C)C
(2S, 4R)-1-(t-Butoxycarbonyl)-4-methanesulfonyloxy-2-methylcarbamoylpyrrolidine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITat 15° C. for 30 minutes
  2. 2
    استخلاصextracted with ethyl acetate
  3. 3
    غسيلThe extract was washed with an aqueous solution of sodium chloride
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    أخرىThe solvent was then removed by distillation under reduced pressure

الإجراء التجريبي

7.11 ml of triethylamine were added, whilst ice-cooling, to a solution of 11.29 g of (2S, 4R)-1-(t-butoxycarbonyl)-2-methylcarbamoyl-4-hydroxypyrrolidine [prepared as described in step (1) above] dissolved in 120 ml of dry tetrahydrofuran, and then 3.93 ml of methanesulfonyl chloride were added to the resulting mixture, and the mixture was stirred at 0° to 5° C. for 30 minutes and then at 15° C. for 30 minutes. It was then 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. The solvent was then removed by distillation under reduced pressure, giving 11.58 g of the title compound as colorless crystals.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242914uspto-grants-1993_09