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HRID 1028943作成日:2026年10月27日

Potassium Phosphate, Tribasic → 6-(2-(3,4-Dihydroisoquinolin-1-yl)-6-methylphenyl)-3-morpholinoquinolin-2-amine

https://huagongshe.com/reaction/1028943

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
反応物1-(2-Bromo-3-methylphenyl)-3,4-dihydroisoquinolineHCID 67324653—
反応物3-Morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amineHCID 67347995—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物6-(2-(3,4-Dihydroisoquinolin-1-yl)-6-methylphenyl)-3-morpholinoquinolin-2-amineHCID 67324753—

反応条件

温度140 °C

反応手順

A mixture of 3-morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine (0.18 g, 0.50 mmol), 1-(2-bromo-3-methylphenyl)-3,4-dihydroisoquinoline (0.10 g, 0.33 mmol), potassium phosphate (0.354 g, 1.67 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (0.032 g, 0.067 mmol) and Pd2 dba3 (0.015 g, 0.017 mmol) were treated with dioxane (2.22 mL) and Water (1.11 mL) in a medium-sized Smith synthesizer vial. The mixture was heated to 140° C. for 12 min in a microwave reactor. The reaction mixture was filtered then partitioned between EtOAc and water. The organic layers were washed with water and brine and then concentrated in vacuo. The crude product was purified by silica flash chromatography (1-10% MeOH:DCM) and then by HPLC (10-75% acetonitril/H2O; TFA modifier). A single fraction was treated with NH4OH, concentrated, filtered and air-dried to afford 6-(2-(3,4-dihydroisoquinolin-1-yl)-6-methylphenyl)-3-morpholinoquinolin-2-amine MS (ESI, pos. ion) m/z: 449 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08735384B2
出典データセットuspto-grants-2014_05
ORD IDord-22cbe4354802463cb1fced1fe3a67e7e
出典メモuspto-grants-2014_05