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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704261Generated: October 29, 2026

Potassium Carbonate → Benzhydryl 7-formamido-3-mesyloxy-3-cephem-4-carboxylate

https://huagongshe.com/reaction/704261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylateHCID 88528581—
SolventDimethylformamideHCID 6228—
ProductBenzhydryl 7-formamido-3-mesyloxy-3-cephem-4-carboxylateHCID 88528775—

Reaction Conditions

Temperature-30 °C

Reaction Steps

Mesyl chloride (0.66 ml) and potassium carbonate (1.38 g) were added to a solution of benzhydryl 7-formamido-3-hydroxy-3-cephem-4-carboxylate (2.05 g) in N,N-dimethylformamide (6 ml) at -30° C. The mixture was stirred at -30° C. for 30 minutes. Mesyl chloride (0.4 ml) was added to the mixture. The reaction mixture was stirred at -30° C. for 20 minutes, poured into ice-water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and filtered, and the filtrate was evaporated in vacuo. The residue was dissolved in a small amount of ethyl acetate and the mixture was subjected to column chromatography on silica gel and eluted with a mixture of benzene and ethyl acetate (1:1). The eluent was evaporated in vacuo. The residue was triturated with diisopropyl ether to give benzhydryl 7-formamido-3-mesyloxy-3-cephem-4-carboxylate (0.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985555
Source datasetuspto-grants-1991_01
ORD IDord-0da1846da2e04d90ae4f05bb7803ae7f
Source noteuspto-grants-1991_01