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HRID 49884作成日:2026年10月26日

3-Chloro-4-fluoroaniline → 1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/49884

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-fluoroanilineHCID 9708—
反応物Triethylamine hydrochlorideHCID 11130—
反応物Sodium HydroxideHCID 14798—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazineHCID 9799193—

反応条件

温度200 °C

反応手順

A mixture of 1.42 g (10 mmol) phosphorus pentoxide, 1.38 g (10 mmol) triethylamine hydrochloride, and 1.46 g (10 mmol) 3-chloro-4-fluoroaniline is heated and stirred in a nitrogen atmosphere at 200° C. until a homogeneous melt has formed. To the melt, 0.593 g (2.5 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 3 h at 200° C. After cooling to RT, the hyalinocrystalline reaction mixture is distributed between 150 ml dichloromethane and a mixture of 10 ml water and 20 ml 2N sodium hydroxide solution with intensive stirring and sonication. The organic phase washed with water and dried over sodium sulfate is concentrated by evaporation and the residue recrystallized from acetate. Title compound is obtained after a second recrystallization from methanol/water and drying under HV (8 h at 100° C.); m.p. 185-187° C.; ESI-MS: (M+H)+=365.

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-8dbc3bce22d84d228a83e727e949ad00
出典メモuspto-grants-2004_03