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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057675Generated: October 26, 2026

4-Aminoacetanilide → 1-(4-Acetaminoanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/1057675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminoacetanilideHCID 31230—
Reactant1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
Solvent1-ButanolHCID 263—
Product1-(4-Acetaminoanilino)-4-(4-pyridylmethyl)phthalazineHCID 22741957—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 0.901 g (6 mmol) 4-aminoacetanilide and 5 ml 1-butanol is heated for 3 h at 110° C. The reaction mixture is then evaporated under vacuum, the crystalline residue is taken up in a mixture of 20 ml dichloromethane and 10 ml 20% aqueous potassium carbonate solution while stirring, then filtered and the filter residue washed with water and dichloromethane. After recrystallization from dichloromethane/methanol and drying under HV (8 h, 100° C.), title compound is obtained with a methanol content of 1.27%;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514974B2
Source datasetuspto-grants-2003_02
ORD IDord-1fe745ced64f4f25a3fc3e3939787b58
Source noteuspto-grants-2003_02