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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770488Generated: November 1, 2026

Cyanoacetic acid → 2-cyano-N-(5-phenyl-1,3,4-thiadiazol-2-yl)acetamide

https://huagongshe.com/reaction/1770488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
Reactant2-Amino-5-phenyl-1,3,4-thiadiazoleHCID 219408—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventHydrochloric AcidHCID 313—
SolventAcetonitrileHCID 6342—
Product2-cyano-N-(5-phenyl-1,3,4-thiadiazol-2-yl)acetamideHCID 57422409—

Reaction Steps

5-phenyl-1,3,4-thiadiazol-2-amine (600 mg, 3.3 mmol), cyano acetic acid (300 mg, 3.6 mmol), and EDC-HCl (861 mg, 4.5 mmol) were stirred in acetonitrile (15 mL) at room temperature for 2 hours. The mixture was diluted with aqueous 1N HCl and the aqueous phase was extracted with ethyl acetate. The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with ethyl acetate/hexanes (1/9) to afford 2-cyano-N-(5-phenyl-1,3,4-thiadiazol-2-yl)acetamide as a white solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09247759B2
Source datasetuspto-grants-2016_02
ORD IDord-570cc52328014746a1f0976c5f277c69
Source noteuspto-grants-2016_02