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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249604Generated: October 28, 2026

Hydrochloric Acid → HCID 178525027, compound

https://huagongshe.com/reaction/249604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
ReactantHCID 178511754HCID 178511754—
ReactantHCID 178526193HCID 178526193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178525027HCID 17852502771%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 7β-amino-3-(1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4-carboxylic acid diphenylmethyl ester (550 mg : 1.08 mMol.) and difluoromethylthioacetic acid (160 mg : 1.13 mMol.) in dichloromethane (8 ml) cooling at -30° C. are added N-methylmorpholine (0.27 ml : 2.46 mMol.) and phenyl dichlorophosphate (0.19 ml : 1.27 mMol.), and the mixture is stirred at -30° C. for 1 hour. The reaction mixture is mixed with 10% hydrochloric acid (1 ml), diluted with water, and extracted with ethyl acetate. The extract is washed with aqueous saline, dried over sodium sulfate, and concentrated. The residue is purified by silica gel column chromatography (toluene : ethyl acetate=1:1) to give 7β-difluoromethylthioacetamido-3-(1,2,3-triazol-4-ylthiomethyl- thio) -3-cephem-4-carboxylic acid diphenylmethyl ester (475 mg) as pale yellow foam. Yield : 69%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214037
Source datasetuspto-grants-1993_05
ORD IDord-83f9c8dd0ec8417bb815acce618ee860
Source noteuspto-grants-1993_05