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HRID 454934作成日:2026年10月26日

Propargyl alcohol → 3-(3-((1-(Quinolin-2-YL)azetidin-3-YL)oxy)pyrazin-2-YL)prop-2-YN-1-OL

https://huagongshe.com/reaction/454934

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl alcoholHCID 7859—
反応物TriethylamineHCID 8471—
反応物2-(3-(3-Chloropyrazin-2-yloxy)azetidin-1-yl)quinolineHCID 58547697—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
生成物3-(3-((1-(Quinolin-2-YL)azetidin-3-YL)oxy)pyrazin-2-YL)prop-2-YN-1-OLHCID 58547699600%

反応条件

温度110 °C

反応手順

A microwave tube was charged with 2-(3-((3-chloropyrazin-2-yl)oxy)azetidin-1-yl)quinoline (see PREPARATION P2.6; 150 mg, 0.5 mmol), triethylamine (100 mg, 1.0 mmol), CuI (10 mg, 0.05 mmol), Pd (PPh3)2Cl2 (35 mg, 0.05 mmol), prop-2-yn-1-ol (28 mg, 0.05 mmol). After several cycles of vacuum/purge with argon, 2 mL of DMF are added. The reaction mixture is then stirred at 110° C. under microwave for 2 hours. The reaction mixture is poured onto a solution of NaHCO3 and diluted with EtOAc and the layers are separated. The organic extracts were washed with water (10 mL) and brine (10 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (5% to 30% EtOAc in petroleum ether) to give the title product (99 mg, 0.3 mmol, 61% yield) as white solid. ESI-MS (M+1): 333 calc. for C19H16N4O2 332.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497265B2
出典データセットuspto-grants-2013_07
ORD IDord-bce3d9b9183341fa93009bcbf97a746a
出典メモuspto-grants-2013_07