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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851608Generated: October 29, 2026

Acetic Acid → 2-Methyl-7-[2-(1,3,4-thiadiazol-2-ylthio)-acetamido]-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/851608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl AcetateHCID 8857—
Reactant2,2,2-Trichloroethyl 2-methyl-7-[2-(1,3,4-thiadiazol-2-yithio)acetamido]-3-cephem-4-carboxylateHCID 12834015—
CatalystZincHCID 23994—
SolventDimethylformamideHCID 6228—
Product2-Methyl-7-[2-(1,3,4-thiadiazol-2-ylthio)-acetamido]-3-cephem-4-carboxylic acidHCID 1283401843.6%

Reaction Steps

Acetic acid (8 ml) and zinc powder (6 g) were added under stirring and ice-cooling to a solution of 2,2,2-trichloroethyl 2-methyl-7-[2-(1,3,4-thiadiazol-2-ylthio)-acetamido]-3-cephem-4-carboxylate (4.65 g) in anhydrous dimethylformamide (30 ml), and the mixture was stirred for 1 hour at the same temperature. After the reaction, ethyl acetate (150 ml) was added to the reaction mixture. The insoluble material was filtered off, and the filtrate was washed with 5% hydrochloride acid saturated with sodium chloride, and then extracted with a sodium bicarbonate aqueous solution. The extract was acidified with 10% hydrochloric acid and extracted with ethyl acetate, after which the ethyl acetate layer was washed with a saturated sodium chloride aqueous solution and dried over magnesium sulfate. After the solvent was distilled off, the residue was recrystallized from a mixture of ethyl acetate and benzene to give 2-methyl-7-[2-(1,3,4-thiadiazol-2-ylthio)-acetamido]-3-cephem-4-carboxylic acid (1.5 g), mp 197° to 199° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04385176
Source datasetuspto-grants-1983_05
ORD IDord-cd7e7608428c487ca0b4cb751d6e198d
Source noteuspto-grants-1983_05