تفاعل #5163

ord-2a56e9a0f2494ea49832784e8b43d622

معادلة التفاعل

[Cl-].[Na+]
sodium chloride
CS(=O)(=O)Cl
methanesulfonyl chloride
CC(C)(C)OC(=O)N1C[C@H](O)C[C@H]1C(N)=O
(2S, 4R)-1-(t-butoxycarbonyl)-2-carbamoyl-4-hydroxypyrrolidine
CCN(CC)CC
triethylamine
CC(C)(C)OC(=O)N1C[C@H](OS(C)(=O)=O)C[C@H]1C(N)=O
title compound
CC(C)(C)OC(=O)N1C[C@H](OS(C)(=O)=O)C[C@H]1C(N)=O
(2S, 4R)-1-(t-Butoxycarbonyl)-2-carbamoyl-4-methanesulfonyloxypyrrolidine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate
  2. 2
    غسيلThe extract was washed with an aqueous solution of sodium chloride
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    أخرىthe solvent was removed by distillation under reduced pressure
  5. 5
    أخرىThe residue was purified by chromatography through silica gel (
  6. 6
    غسيلeluted 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.

المصدر

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