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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49885Generated: October 25, 2026

Ammonia → 1-(3-Methylanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/49885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactantm-ToluidineHCID 7934—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantTetramethylureaHCID 12437—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(3-Methylanilino)-4-(4-pyridylmethyl)phthalazineHCID 6419387—

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 2.39 g (16.8 mmol) phosphorus pentoxide, 2.31 g (16.8 mmol) triethylamine hydrochloride, and 1.82 ml (16.8 mmol) m-toluidine is heated and stirred in a nitrogen atmosphere at 200° C. until a homogeneous melt has formed. To the melt, 1 g (4.2 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 3.5 h at 205° C. After cooling to about 170° C., 4 ml tetramethylurea is added to the reaction mixture, followed by 2 ml water at about 110° C. The mixture is stirred for a further 30 min while cooling to RT and then distributed between dichloromethane and a mixture of 20 ml water and 5 ml conc. ammonia. The organic phase dried over sodium sulfate is concentrated by evaporation and the residue purified on silica gel by flash chromatography using acetate and acetate/methanol (99:1 and 19:1). Title compound is obtained after crystallization of the product-containing fractions from acetonitrile and subsequent recrystallization from acetate; m.p. 141-143° C.; ESI-MS: (M+H)+=327.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710047B2
Source datasetuspto-grants-2004_03
ORD IDord-2d57d14ff339450ebd4864938eadbeb0
Source noteuspto-grants-2004_03