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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543534Generated: October 25, 2026

Dacthal → 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid hydrochloride

https://huagongshe.com/reaction/543534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDacthalHCID 2943—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantHCID 178482017HCID 178482017—
SolventAcetonitrileHCID 6342—
Product7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid hydrochlorideHCID 70463764103.4%

Reaction Conditions

Temperature15 °C

Reaction Steps

A 11 ml portion of acetonitrile was added to 2.72 g of 7-ACA and 1.28 g of 5-mercapto-1-methyl-1H-tetrazole, and 14.9 g of DCPA was added through a dropping funnel to the mixture with stirring and under cooling at -25° to -20° C., followed by rinsing the funnel with 1 ml of acetonitrile. The reaction mixture was warmed to 15° C., stirred at 14° to 16° C. for 40 minutes and cooled to -30° C., followed by adding dropwise 40 ml of ethanol at -30° to -20° C. The resultant solution was warmed to room temperature, and stirred under ice-cooling for 3.0 hours after the addition of 300 ml of methylene chloride, 100 ml of ether and 70 ml of ether saturated with water. The crystals separated out were recovered by filtration, washed with ether and dried, thereby affording 3.77 g (86.0% of purity as determined by high performance liquid chromatography, 88.9% of yield) of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446318
Source datasetuspto-grants-1984_05
ORD IDord-46b479af67774d569c2efe4f247833c4
Source noteuspto-grants-1984_05