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HRID 49909作成日:2026年10月24日

Water → 1-(3-Chlorophenoxy)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/ja/reaction/49909

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-ChlorophenolHCID 7933—
反応物Potassium CarbonateHCID 11430—
反応物1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物1-(3-Chlorophenoxy)-4-(4-pyridylmethyl)phthalazineHCID 22742020—

反応手順

Under exclusion of air, 200 mg (0.78 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine (Example 67A.1), 173 mg (1.25 mmol) K2CO3, and 120 mg (0.94 mmol) 3-chlorophenol (Fluka) are heated in 2 ml DMSO for 3 h to 90° C. The reaction mixture is distributed between 20 ml water and 20 ml ethyl acetate, and the aqueous phase separated and extracted with 2 portions of ethyl acetate. The organic phase is washed with water and brine, dried (MgSO4), and concentrated by evaporation. The residue is dissolved in ≦15 ml THF, precipitated with hexane, and filtered. Title compound is obtained from the evaporated filtrate after chromatography (SiO2; ethyl acetate/CH3OH, 4:1): m.p.: 143-145° C.; HPLC: tRet(Grad20-100)=8.9; FAB MS (M+H)+=348.

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-463d73f1d89a47c8b2e0d1e69b67737c
出典メモuspto-grants-2004_03