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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49865Generated: October 23, 2026

Acetate → 1-(3-Pyridylamino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/en/reaction/49865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
Reactant3-AminopyridineHCID 10009—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
Product1-(3-Pyridylamino)-4-(4-pyridylmethyl)phthalazineHCID 22742008—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 0.565 g (6 mmol) 3-aminopyridine is heated for 3 h at 90° C. The residue is then distributed between acetate and 20% aqueous potassium carbonate solution. The organic phase dried over anhydrous sodium sulfate is evaporated and the residue purified on silica gel by flash chromatography using acetate/methanol mixtures (49:1 to 4:1). Title compound is obtained after crystallization of the product-containing fractions from acetonitrile and drying under HV (6 h, 80° C.); m.p. 137-139° C.; ESI-MS: (M+H)+=314.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710047B2
Source datasetuspto-grants-2004_03
ORD IDord-f462d2582a3e4670a175fc0c7446c18b
Source noteuspto-grants-2004_03