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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463655Generated: October 30, 2026

6-(4-Aminophenyl)-4,5-dihydropyridazin-3(2H)-one → HCID 13193380, compound

https://huagongshe.com/reaction/463655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-Aminophenyl)-4,5-dihydropyridazin-3(2H)-oneHCID 676750—
Reactant2-Cyanoacetyl chlorideHCID 11051594—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13193380HCID 1319338054.2%

Reaction Steps

5.9 g (57.0 millimoles) of cyanoacetyl chloride were added dropwise to 6.0 g (31.7 millimoles) of 6-(p-aminophenyl)-4,5-dihydro-3(2H)-pyridazinone in 150 ml of absolute tetrahydrofuran at room temperature, while stirring. After the addition was complete, stirring was continued for a further 10 minutes at 50° C. The product was filtered off under suction at 10° C., washed first with tetrahydrofuran and then with water and recrystallized from dimethylformamide/water. 4.4 g (54%) of 6-[p-(cyanoacetylamino)-phenyl]-4.5,-dihydro-3(2H)-pyridazinone were obtained as pale beige crystals. Mp.: 270° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544562
Source datasetuspto-grants-1985_10
ORD IDord-94ed8b954ebf4babac871bcc0ed0f9f7
Source noteuspto-grants-1985_10