戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 245745作成日:2026年10月26日

Dichloromethane → HCID 178487940、化合物

https://huagongshe.com/reaction/245745

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Potassium CarbonateHCID 11430—
反応物2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 17750207—
反応物HCID 178432912HCID 178432912—
溶媒AcetonitrileHCID 6342—
溶媒1,4-DioxaneHCID 31275—
生成物HCID 178487940HCID 17848794037.1%

反応条件

温度89 °C

反応手順

To a suspension of 1-bromo-8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazine (0.714 mmol, 280 mg) and 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (0.714 mmol, 178 mg) in dioxane (5 mL) was added aqueous 2M potassium carbonate (3.57 mmol, 1.78 mL). The mixture was degassed and put under a nitrogen atmosphere. Then 1,1′-bis(diphenylphosphino)ferrocene palladium (II) chloride complex with dichloromethane (0.050 mmol, 40.4 mg) was added and the reaction mixture was heated to 89° C. After three hours the reaction mixture was diluted with acetonitrile (9 ml) and filtered over decalite. The filtrate was concentrated in vacuo and the residue was purified by column chromatography (silica gel; gradient of dichloromethane to dichloromethane/methanol 5/1) to give 2-methoxy-4-(8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazin-1-yl)aniline (115 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658794B2
出典データセットuspto-grants-2014_02
ORD IDord-13660ae0602c4d3fa3e8d6f6075710bc
出典メモuspto-grants-2014_02