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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707444Generated: October 26, 2026

Hydrochloric Acid → HCID 178511753, compound

https://huagongshe.com/reaction/1707444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantTrityl chlorideHCID 6456—
Reactant1,3-ButanediolHCID 7896—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 178520256HCID 178520256—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178511753HCID 17851175356%

Reaction Steps

To a solution of 7β-phenylacetamido-3-(1,2,3-triazol-4-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester (10.0 g: 15.9 mMol.) in dichloromethane (100 ml) under ice cooling are added pyridine (1.54 ml: 19.1 mMol.) and trityl chloride (5.32 g: 19.1 mMol.), and the mixture is stirred at room temperature for 1 hour. The reaction mixture is mixed with 10% hydrochloric acid (2 ml), diluted with water, and extracted with ethyl acetate. The extract is washed with water, dried over sodium sulfate, and concentrated. To a solution of the residue in dichloromethane (50 ml) under ice cooling are added pyridine (2.57 ml: 31.8 mMol.) and phosphorus pentachloride (5.96 g: 28.6 mMol.), and the mixture is stirred for 30 minutes. The reaction mixture is added dropwise to a solution of 1.3-butanediol (8.6 ml: 95.9 mMol.) in dichloromethane (25 ml) at -30° C., and the mixture is stirred at - 20° to -30° C. for 10 minutes and under ice cooling for 40 minutes. The reaction mixture is mixed with water, diluted with dichloromethane, washed with brine, dried over sodium sulfate, and concentrated. The residue is pulverized with ether, washed with ether, dissolved in dichloromethane, washed with 5% aqueous sodium hydrogen carbonate, dried over sodium sulfate, and concentrated. The residue is purified by silica gel chromatography (toluene: ethyl acetate=2:1) to give 7β-amino-3-(trityl-1,2,3-triazol-4-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester (6.70 g: pale yellow foam, Yield: 56%,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352792
Source datasetuspto-grants-1994_10
ORD IDord-f5876e6c842247fa8f8676160c18b50b
Source noteuspto-grants-1994_10