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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258771Generated: November 1, 2026

Hydrochloric Acid → HCID 21426475, compound

https://huagongshe.com/reaction/258771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 21426457HCID 21426457—
ReactantHCID 88827510HCID 88827510—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
ProductHCID 21426475HCID 2142647523.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-Acetoxymethyl-2-carboxy-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (7 g.) is dissolved in distilled water (100 cc.) and sodium bicarbonate (1.46 g.). A solution of 5-ethyl-2-thioxo-1,3,4-thiadiazoline (2.63 g.) in distilled water (60 cc.) and sodium bicarbonate (1.46 g.) is added and the resulting solution is heated to 60° C. for 6 hours. After cooling, it is acidified to pH 5.5 by adding 4 N hydrochloric acid and is then extracted twice with ethyl acetate (100 cc.). The organic extracts are discarded. The acidification is continued in the presence of ethyl acetate (300 cc.) until the pH is 2. After decanting the organic phase, the aqueous phase is extracted twice with ethyl acetate (a total of 200 cc.). The combined organic extracts are washed twice with water (200 cc.), dried over magnesium sulphate, treated with decolourising charcoal and then filtered and concentrated to dryness under reduced pressure (20 mm.Hg). The residue obtained is recrystallised from methanol (100 cc.) to give 2-carboxy-3-[(5-ethyl-1,3,4-thiadiazol-2-yl)-thiomethyl]-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (2 g.) m.p. 155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034090
Source datasetuspto-grants-1977_07
ORD IDord-55e8c97712f64f40aab4a757a24ede8f
Source noteuspto-grants-1977_07