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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057709Generated: October 25, 2026

4-Aminobiphenyl → N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine

https://huagongshe.com/reaction/1057709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobiphenylHCID 7102—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantCarbonate IonHCID 19660—
Reactant4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
SolventWaterHCID 962—
SolventDichloromethane methanolHCID 21226129—
ProductN-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amineHCID 6419389—

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 2.41 g (16.98 mmol) phosphorus pentoxide, 2.32 g (16.85 mmol) triethylamine hydrochloride, 3 g (17.73 mmol) 4-aminobiphenyl, and 1 g (4.21 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is stirred for 20 h at 200° C. under a nitrogen atmosphere. After cooling to RT, the hyalinocrystalline melt is distributed between a dichloromethane/methanol mixture (99:1) and a mixture of water and saturated aqueous carbonate solution (1:1) with intensive stirring and the use of an ultrasonic bath. The organic phase dried over sodium sulfate is evaporated under vacuum and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using a dichloromethane/methanol mixture (49:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and recrystallization of the residue from acetonitrile; m.p. 189-191° C.; ESI-MS: (M+H)+=389.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514974B2
Source datasetuspto-grants-2003_02
ORD IDord-383323b6e4fb4916aaabfa63371d3f2f
Source noteuspto-grants-2003_02