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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384106Generated: October 25, 2026

3-Aminophenol → 1-(3-Hydroxyanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/1384106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
Reactant1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
SolventAcetateHCID 175—
SolventMethanolHCID 887—
SolventPotassium CarbonateHCID 11430—
Product1-(3-Hydroxyanilino)-4-(4-pyridylmethyl)phthalazineHCID 6419391—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 0.384 g (1.5 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 0.491 g (4.5 mmol) 3-aminophenol is heated under nitrogen atmosphere for 1 h at 90° C. and for 3 h at 120° C. The reaction mixture is then taken up in a mixture of 30 ml acetate and 20 ml 20% aqueous potassium carbonate solution while stirring for about 4 h, and the filtration material is digested for 20 min in 20 ml of boiling methanol. After cooling to RT, filtration, washing of the filter residue with methanol, and drying under HV (8 h, 130° C.), title compound is obtained with a water content of 1.94%; m.p. 217-219° C.; ESI-MS: (M+H)+=329.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258812B1
Source datasetuspto-grants-2001_07
ORD IDord-aee4695973b343dca4b94d8387dcfc84
Source noteuspto-grants-2001_07