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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49884생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/49884

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-4-fluoroanilineHCID 9708—
반응물Triethylamine hydrochlorideHCID 11130—
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazineHCID 9799193—

반응 조건

온도200 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710047B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-8dbc3bce22d84d228a83e727e949ad00
출처 메모uspto-grants-2004_03