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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658652Generated: October 28, 2026

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

https://huagongshe.com/reaction/658652

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 numberUS08076491B2
Source datasetuspto-grants-2011_12
ORD IDord-49a5e7f510d847bfab5c7ecbc31f42b8
Source noteuspto-grants-2011_12