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HRID 589909作成日:2026年10月26日

Triethylamine → 6-[(4-Aminophenyl)ethynyl]imidazo[1,2-b]pyridazin-2-amine

https://huagongshe.com/reaction/589909

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-EthynylanilineHCID 3760025—
反応物6-Iodoimidazo[1,2-B]pyridazin-2-amineHCID 57441024—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物6-[(4-Aminophenyl)ethynyl]imidazo[1,2-b]pyridazin-2-amineHCID 118638446—

反応条件

温度50 °C

反応手順

To the mixture of 6-iodo-imidazo[1,2-b]pyridazin-2-ylamine (780 mg, 3.0 mmol, 1 eq) and 4-ethynylaniline (543 mg, 1.5 eq) in anhydrous DMF (10 mL) under nitrogen atmosphere was added triethylamine (1.67 mL, 4 eq), bis(triphenylphosphine)palladium(II) dichloride (210 mg, 0.1 eq) and copper(I) iodide (114 mg, 0.2 eq). After the reaction mixture was stirred at 50° C. for 30 minutes, it was partitioned between saturated aqueous sodium bicarbonate and chloroform (containing 3% v/v of MeOH). The organic layer was separated and washed with aqueous ammonium chloride, brine, and lastly dried with anhydrous sodium sulfate. The upper suspension mixture was decanted, concentrated, and the solid residue was subject to a gradient column chromatography (from CHCl3 to MeOH—CHCl3 1:30) to give 6-[(4-aminophenyl)ethynyl]imidazo[1,2-b]pyridazin-2-amine as a yellow solid in amount of 166 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09233968B1
出典データセットuspto-grants-2016_01
ORD IDord-a7aa7a3cad184936abfc3a827735dd59
出典メモuspto-grants-2016_01