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HRID 49891作成日:2026年10月26日

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

https://huagongshe.com/reaction/49891

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminobiphenylHCID 7102—
反応物Triethylamine hydrochlorideHCID 11130—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物Carbonate IonHCID 19660—
反応物4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
溶媒WaterHCID 962—
溶媒Dichloromethane methanolHCID 21226129—
生成物N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amineHCID 6419389—

反応条件

温度200 °C

反応手順

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 on (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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710047B2
出典データセットuspto-grants-2004_03
ORD IDord-68d8d685ff174f3fb8764293eccc5175
出典メモuspto-grants-2004_03