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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030129Erstellt: 26. Oktober 2026

Sodium Chloride → (2S, 4R)-1-(t-Butoxycarbonyl)-2-carbamoyl-4-methanesulfonyloxypyrrolidine

https://huagongshe.com/reaction/1030129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt(2S,4R)-1-Boc-2-carbamoyl-4-hydroxypyrrolidineHCID 14796648—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2S, 4R)-1-(t-Butoxycarbonyl)-2-carbamoyl-4-methanesulfonyloxypyrrolidineHCID 14880263—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05104867
Quelldatensatzuspto-grants-1992_04
ORD IDord-81b35a72c22144a3b3e6601a02c7f0a8
Quellennotizuspto-grants-1992_04