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HRID 3233作成日:2026年10月24日

(3-Chloropropyl)benzene → 2-Amino-6-(2,6-dichlorophenyl)-8-(3-phenylpropyl)-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/ja/reaction/3233

反応式

関与物質

役割名称HCID仕込み量
反応物(3-Chloropropyl)benzeneHCID 7706—
反応物Sodium hydrideHCID 24758—
反応物2-Amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-olHCID 10494915—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-Amino-6-(2,6-dichlorophenyl)-8-(3-phenylpropyl)-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 1168328957.2%

反応条件

温度60 °C

反応手順

To a suspension of NaH (60% in mineral oil, 58 mg) in 10 mL of dimethylformamide was added 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one (320 mg, 1.04 mmol). The mixture was heated to 60° C. resulting in a clear solution. 1-Chloro-3-phenylpropane (260 μL, 1.81 mmol) was added, and the reaction mixture was heated at 60° C. for 35 minutes, then poured onto ice water. The resulting gummy solid was dissolved in ethyl acetate, washed with water, and dried over magnesium sulfate. Filtration, followed by concentration in vacuo, gave an oil that was purified by flash chromatography, eluting with 1:3 hexane:ethyl acetate to provide 345 mg of crude product. Recrystallization from ethyl acetate and hexane followed by drying in vacuo provided 253 mg (57%) of 2-amino-6-(2,6-dichlorophenyl)-8-(3-phenylpropyl)-8H-pyrido[2,3-d]pyrimidin-7-one; mp 161°-163° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733914
出典データセットuspto-grants-1998_03
ORD IDord-ce2698e35bd94905bfdf55ec0d5c3c0a
出典メモuspto-grants-1998_03