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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454934생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl alcoholHCID 7859—
반응물TriethylamineHCID 8471—
반응물2-(3-(3-Chloropyrazin-2-yloxy)azetidin-1-yl)quinolineHCID 58547697—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
생성물3-(3-((1-(Quinolin-2-YL)azetidin-3-YL)oxy)pyrazin-2-YL)prop-2-YN-1-OLHCID 58547699600%

반응 조건

온도110 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497265B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-bce3d9b9183341fa93009bcbf97a746a
출처 메모uspto-grants-2013_07