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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686264Generated: November 1, 2026

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

https://huagongshe.com/reaction/1686264

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 numberUS08148544B2
Source datasetuspto-grants-2012_04
ORD IDord-80815b3845a24853b8ed39ac3ad0afe5
Source noteuspto-grants-2012_04