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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043668Generated: November 1, 2026

Ethylamine → HCID 67335526, compound

https://huagongshe.com/reaction/1043668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTriethylamineHCID 8471—
ReactantHCID 47003642HCID 47003642—
SolventAcetonitrileHCID 6342—
ProductHCID 67335526HCID 67335526—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-imidazo[2,1-b][1,3,4]thiadiazole-5-sulfonyl chloride (0.15 g; 0.50 mmol) was dissolved in dry acetonitrile (5 mL). Triethylamine (69 μL; 0.50 mmol) was added, and the reaction mixture was cooled at 0° C. for 10 minutes before adding ethylamine (2M in tetrahydrofuran, 2.5 mL; 5.0 mmol). The reaction was allowed to reach room temperature and stirred overnight. The solvent was evaporated and the crude taken up in dichloromethane and sodium hydrogen carbonate solution. Extraction with dichloromethane, drying over sodium sulphate and evaporation of the solvent gave a brown gum that was purified on silica gel (ethyl acetate:hexane 4:1). The title product 2-ethylamino-imidazo[2,1-b][1,3,4]thiadiazole-5-sulfonic acid ethylamide was isolated as a white powder (43 mg, 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563550B2
Source datasetuspto-grants-2013_10
ORD IDord-f179cac0692043e5b821c89e55ca6bd8
Source noteuspto-grants-2013_10