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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255892Generated: October 30, 2026

3-Pyridinecarboxaldehyde → 3-[5-(4-Chlorophenyl)-2,3-dihydro-1,3,4-thiadiazol-2-yl]pyridine

https://huagongshe.com/reaction/255892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
Reactant4-Chloro-thiobenzoic acid hydrazideHCID 12477075—
SolventEthanolHCID 702—
Product3-[5-(4-Chlorophenyl)-2,3-dihydro-1,3,4-thiadiazol-2-yl]pyridineHCID 15708363—

Reaction Steps

39.2 g of p-chlorothiobenzoic acid hydrazide are dissolved in 350 ml of ethanol. Under nitrogen, 21.4 g of pyridine-3-aldehyde (dissolved in 20 ml of ethanol) are added dropwise to this solution. The reaction temperature is kept at 20° C. by cooling. When the addition is complete, the reaction mixture is stirred for 1 hour at reflux temperature and subsequently filtered through finely particulate diatomaceous earth. The filtrate is concentrated to three quarters of its initial volume and the precipitated product is isolated by filtration, washed with hexane and dried, affording the title compound of the formula ##STR8## with a melting point of 106°-108° C. (compound 1.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699913
Source datasetuspto-grants-1987_10
ORD IDord-1be53cd740d54dbea094fc9e3c17a57f
Source noteuspto-grants-1987_10