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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435969Generated: October 29, 2026

Sodium Bicarbonate → HCID 21454863, compound

https://huagongshe.com/reaction/435969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Methyl-1,3,4-thiadiazole-2(3H)-thioneHCID 1810203—
ReactantSodiumHCID 5360545—
ReactantHCID 21454860HCID 21454860—
SolventWaterHCID 962—
ProductHCID 21454863HCID 2145486345.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

The sodium salt of 3-acetoxymethyl-2-carboxy-7-[(5,6-dihydro-1,4-oxathiin-2-yl )acetamido]-8-oxo-5-thia-1-aza-bicyclo[4,2,0]oct-2-ene (14 g.) is dissolved in distilled water (350 cc.). Sodium bicarbonate (2.69 g.) followed by 2-methyl-5-thioxo-1,3,4-thiadiazoline (4.65 g.) are added to the solution and the reaction mixture is heated with stirring at 60° C. for 6 hours. After cooling, the reaction mixture is washed with ethyl acetate (2 × 150 cc.) and then acidified to pH 2 by addition of 4N hydrochloric acid in the presence of ethyl acetate (350 cc.). After decanting the organic phase, the aqueous phase is extracted twice with ethyl acetate (total 150 cc.). The organic extracts are combined, washed six times with water (total 600 cc.), dried over sodium sulphate, treated with decolourizing charcoal, filtered and then concentrated under reduced pressure (20 mm.Hg) to a final volume of 80 cc. After 30 minutes at 2° C., the solid compound which has formed is filtered off and then washed twice with ethyl acetate (10 cc.) and finally with diisopropyl ether (100 cc.). After drying under reduced pressure (0.5 mm.Hg), 2-carboxy-7-[(5,6-dihydro-1,4-oxathiin-2-yl )acetamido]-3-[(5-methyl-1,3,4-thiadiazol-2-yl )thiomethyl]-8-oxo-5-thia-1-aza-bicyclo[4,2,0]oct-2-ene (7.5 g.) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007176
Source datasetuspto-grants-1977_02
ORD IDord-449d40d588aa418891997b0820250faf
Source noteuspto-grants-1977_02