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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649758Generated: October 26, 2026

Sodium Hydroxide → Sodium 7beta-(2-methylsulfonylethoxycarbonylamino)-3-hydroxymethyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1649758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantCarbonochloridic acid, 2-(methylsulfonyl)ethyl esterHCID 104458—
ReactantSodium BicarbonateHCID 516892—
Reactant(6R-trans)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acidHCID 11031679—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductSodium 7beta-(2-methylsulfonylethoxycarbonylamino)-3-hydroxymethyl-3-cephem-4-carboxylateHCID 67868135—

Reaction Steps

In 50 ml of water is suspended 4.60 g of 7β-amino-3-hydroxymethyl-3-cephem-4-carboxylic acid and, with ice-cooling and stirring, 20 ml of 1N aqueous sodium hydroxide solution is added to the suspension for dissolving the acid. To the solution is added 1.85 g of sodium hydrogen carbonate and, then, a solution of 4.11 g of 2-methylsulfonylethoxycarbonyl chloride in 40 ml of tetrahydrofuran is added dropwise. The mixtrue is stirred with ice-cooling for 2 hours, then adjusted to pH 6.5, washed with ethyl acetate, and concentrated under reduced pressure. The residue is subjected to column chromatography on XAD-II (600 ml). Elution is performed with water and the eluate is concentrated under reduced pressure and freeze-dried to give 3.10 g of sodium 7β-(2-methylsulfonylethoxycarbonylamino)-3-hydroxymethyl-3-cephem-4-carboxylate as light yellow powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921851
Source datasetuspto-grants-1990_05
ORD IDord-99c18f30ea1e46b09e7d193242ee47b9
Source noteuspto-grants-1990_05