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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596788Generated: November 1, 2026

Phosphate → 7-Acetoacetamido-3(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/596788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Acetoacetamido-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 88715150—
ReactantHCID 178434161HCID 178434161—
Product7-Acetoacetamido-3(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 131710660—

Reaction Steps

A mixture of 0.356 g. of 7-acetoacetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid, 0.84 g. of sodium hydrogen carbonate, 0.246 g. of 5-methyl-1,3,4-thiadiazol-2-thiol and 20 ml. of a phosphate buffer of pH 6.4 is heated at 60° C for 7.5 hours. After cooling, it is washed with ethyl acetate, adjusted to pH 2 with 50 % phosphoric acid, saturated with sodium chloride and extracted with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and concentrated under reduced pressure, followed by cooling with ice. The resultant crystals are recovered by suction-filtration, washed with hexane and dried. The described procedure gives 7-acetoacetamido-3-(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid as crystals melting at 177°-180° C (decomp.). Yield 0.274 g. (64 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012379
Source datasetuspto-grants-1977_03
ORD IDord-4502d26896f54d8e880428a73e1204c2
Source noteuspto-grants-1977_03