戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1586417作成日:2026年10月27日

Isobutyl iodide → 2-amino-6-(2,6-dichlorophenyl)-8-isobutyl-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/1586417

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutyl iodideHCID 10556—
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—
生成物2-amino-6-(2,6-dichlorophenyl)-8-isobutyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 532862851%

反応条件

温度60 °C

反応手順

To a suspension of NaH (60% in mineral oil, 36 mg) in 8 mL of dimethylformamide was added 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one (205 mg, 0.67 mmol). The mixture was heated at 60° C. for 20 minutes resulting in a clear solution. 1-Iodo-2-methylpropane (110 μL, 0.94 mmol) was added, and the solution was stirred at 50° C. for 30 minutes. An additional amount of 1-iodo-2-methylpropane (40 μL, 0.34 mmol) was added, and the solution was stirred at 50° C. for 40 minutes, then cooled to room temperature and poured onto 40 mL of ice water. The resulting precipitate was removed by filtration and washed with water. The gummy residue was dissolved in ethyl acetate and washed with water. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting solid was purified by flash chromatography, eluting with 1:1 hexane:ethyl acetate to provide 123 mg (51%) of 2-amino-6-(2,6-dichlorophenyl)-8-isobutyl-8H-pyrido[2,3-d]pyrimidin-7-one; mp 193-195° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05945422
出典データセットuspto-grants-1999_08
ORD IDord-5256673fe4434e498da1306f15061f88
出典メモuspto-grants-1999_08