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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254555Generated: November 1, 2026

3-Chloro-6-(3-methoxy-4-propoxyphenyl)pyridazine → HCID 57191541, compound

https://huagongshe.com/reaction/2254555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-(3-methoxy-4-propoxyphenyl)pyridazineHCID 19385494—
ReactantCyanamidnatriumHCID 57375518—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventTolueneHCID 1140—
ProductHCID 57191541HCID 57191541—

Reaction Steps

1.8 g 3-chloro-6-(3-methoxy-4-n-propoxyphenyl)pyridazine, 0.8 g sodium cyanamide and 3.6 g tetrabutylammonium chloride are boiled under reflux in 30 ml dry toluene for 5 hours. The reaction mixture is then evaporated in vacuo and the residue is boiled up briefly with 200 ml 2 N sodium hydrogen sulphate solution, while stirring thoroughly, the reaction product precipitating as a fine crystalline precipitate. The precipitate is filtered off with suction, washed with water and dried in vacuo. For purification, it is boiled up briefly with 50 ml isopropanol, filtered off with suction and dried in vacuo. This gives 1.5 g (83.3%) of the title compound of m.p. 187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236918
Source datasetuspto-grants-1993_08
ORD IDord-e53a373310f0488eb6e4dd1e711822e1
Source noteuspto-grants-1993_08