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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710045Generated: October 30, 2026

Pyridine → HCID 14883432, compound

https://huagongshe.com/reaction/1710045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
Reactant2,4-DimethylthiosemicarbazideHCID 3034187—
SolventDiethyl EtherHCID 3283—
ProductHCID 14883432HCID 14883432—

Reaction Steps

To a stirred, room temperature, solution of 2,4-dimethylthiosemicarbazide (3.75 g, 3.15×10-2 mole) and pyridine (30 ml) was added dropwise 2-thiophenecarbonyl chloride (3.20 ml, 2.99×10-2 mole). After stirring overnight the pyridine was evaporated at reduced pressure and the concentrate was treated with H2O. The resulting semi-solid was extracted into ethyl acetate. The ethyl acetate extract was washed with saturated NaCl and subsequently dried over anhydrous Na2SO4. The drying agent was removed by filtration and the filtrate was evaporated at reduced pressure, leaving a slightly yellowish solid. This was treated with Et2O and the solid was collected by filtration affording a colorless powder: 4.7 g (68%), mp 176°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952593
Source datasetuspto-grants-1990_08
ORD IDord-a6775e3fb1694d95b4c4a0ae53ce811a
Source noteuspto-grants-1990_08