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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447969Generated: November 2, 2026

Triethylamine → 2-(4,5-Dichloro-imidazol-2-yl)-5-amino-1,3,4-thiadiazole

https://huagongshe.com/reaction/1447969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThiosemicarbazideHCID 2723789—
Reactant4,5-Dichloro-2-(trichloromethyl)-1H-imidazoleHCID 12482573—
SolventEthanolHCID 702—
Product2-(4,5-Dichloro-imidazol-2-yl)-5-amino-1,3,4-thiadiazoleHCID 13575544776.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

9.1 g (0.1 mol) of thiosemicarbazide and 40.4 g (0.4 mol) of triethylamine were stirred in 200 ml of ethanol until a clear solution had formed. 25.4 g (0.1 mol) of 4,5-dichloro-2-trichloromethyl-imidazole were added to this solution incrementally at 0°-5° C., while stirring. The mixture was stirred for a further 1 hour with cooling, for 1 hour at room temperature and for 1 hour at 50° C. After cooling, the amine-hydrochloride was filtered off and the filtrate was evaporated in vacuo. The residue was treated with water, the mixture was acidified with hydrochloric acid and the product was filtered off, washed with water and dried. 18 g (76.5% of theory) of 2-(4,5-dichloro-imidazol-2-yl)-5-amino-1,3,4-thiadiazole were obtained. Melting point: 147° C. (with decomposition) (from ethyl acetate/ligroin).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179277
Source datasetuspto-grants-1979_12
ORD IDord-d428a844aae74bd2a1c288981cc598ae
Source noteuspto-grants-1979_12