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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539525생성일: 2026년 10월 27일

Azidobenzene → 1-Phenyltriazolylmethyl-3-methoxypyridine-2-one

https://huagongshe.com/reaction/539525

반응식

참여 물질

역할이름HCID투입량
반응물AzidobenzeneHCID 69319—
반응물DiisopropylethylamineHCID 81531—
반응물1-Propargyl-3-methoxypyridine-2-oneHCID 71655522—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물1-Phenyltriazolylmethyl-3-methoxypyridine-2-oneHCID 17848764292%

반응 단계

150 (0.32 g, 1.951 mmol) and phenylazide (0.348 g, 2.926 mmol) were dissolved in anhydrous THF (10 mL) and stirred under argon at room temperature. Copper (I) iodide (0.011 g, 0.07 mmol) and Hunig's base (0.1 mL) were then added to the reaction mixture, and stirring continued for 4 h. The reaction mixture was diluted with CH2Cl2 (40 mL) and washed with 1:4 NH4OH/saturated NH4Cl (3×30 mL) and saturated NH4Cl (30 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude product was triturated with hexanes to give 510 mg (92%) of white solid 151a. 1H NMR (CDCl3, 400 MHz) δ 3.58 (3H, s), 5.11 (2H, s), 5.93 (1H, t, J=7.6), 6.42 (1H, d, J=7.2), 7.07 (1H, d, J=6.4), 7.16-7.20 (1H, m), 7.26 (2H, t, J=7.6), 7.49 (2H, d, J=8.0); 13C NMR (CDCl3, 100 MHz) δ 44.2, 55.2, 104.7, 112.0, 119.7, 121.8, 127.9, 128.1, 129.0, 136.2, 142.8, 149.3, 157.2. HRMS (EI) calcd for C15H14N4O2 [M]+ 282.1117. found 282.1115.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871728B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-9bf95ba9cb8a4f1ca877deefdf743549
출처 메모uspto-grants-2014_10