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HRID 1045508作成日:2026年10月27日

Cesium carbonate → 3-(4-Methoxy-benzyl)-5-(4-quinoxalin-2-yl-phenoxy)-3,4-dihydro-1H-pyrido[2,3-d]pyrimidin-2-one

https://huagongshe.com/reaction/1045508

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-Quinoxalin-2-ylphenolHCID 787366—
反応物5-chloro-3-[(4-methoxyphenyl)methyl]-1H,2H,3H,4H-pyrido[2,3-d]pyrimidin-2-oneHCID 66926291—
溶媒DimethylformamideHCID 6228—
生成物3-(4-Methoxy-benzyl)-5-(4-quinoxalin-2-yl-phenoxy)-3,4-dihydro-1H-pyrido[2,3-d]pyrimidin-2-oneHCID 7049924142.7%

反応条件

温度130 °C

反応手順

A suspension of 5-chloro-3-(4-methoxy-benzyl)-3,4-dihydro-1h-pyrido[2,3-d]pyrimidin-2-one (100.00 mg; 0.33 mmol; 1.00 eq.), 4-quinoxalin-2-ylphenol (91.46 mg; 0.41 mmol; 1.25 eq.), and cesium carbonate (214.54 mg; 0.66 mmol; 2.00 eq.) in DMF (2.00 ml) was heated in a microwave at 130° C. for 4 hours. The reaction was concentrated, redissolved in DMSO, syringe filtered, and purified via prep HPLC to afford 69 mg of 280 as an off-white solid. LC-MS (M+H=490, obsd.=490).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569295B2
出典データセットuspto-grants-2013_10
ORD IDord-e7b9b692cfe24bcb9cbc699769f3cb7a
出典メモuspto-grants-2013_10