Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323574Generated: October 30, 2026

Ethyl cyanoacetate → HCID 22006193, compound

https://huagongshe.com/reaction/323574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 54095431HCID 54095431—
SolventDichloromethaneHCID 6344—
ProductHCID 22006193HCID 22006193—

Reaction Conditions

Temperature160 °C

Reaction Steps

An intimate, magnetically stirred mixture of 440 mg (1.40 mmol) of 1-[(4-methylphenyl)thio]-1-[(4-methoxyphenyl)hydrazono]-2-propanone 370 μl of ethylcyanoacetate and 178 mg of ammonium acetate was heated under a nitrogen atmosphere at 160° C. for 30 min. The reaction mixture was cooled and dissolved in methylene chloride. The organic layer was washed successively with saturated aqueous sodium bicarbonate and water. The organic layer was dried over magnesium sulfate and evaporated in vacuo to yield semi-pure product. The residue was recrystallized from ethanol to yield 6-[(4-methylphenyl)thio]-2,3-dihydro-2-(4-methoxyphenyl)-5-methyl-3-oxo-4-pyridazinecarbonitrile, mp 148-149° C.(EtOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214810B1
Source datasetuspto-grants-2001_04
ORD IDord-59922d7eea8e40d9a07d4d2c28c44496
Source noteuspto-grants-2001_04