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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33822생성일: 2026년 10월 24일

Acetic Acid → 2-(Pyridin-4-yl)-1-(4-(quinolin-2-ylmethoxy)phenyl)ethan-1-one

https://huagongshe.com/ko/reaction/33822

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-MethylpyridineHCID 7963—
반응물Lithium diisopropylamideHCID 2724682—
반응물Benzamide, N-methoxy-N-methyl-4-(2-quinolinylmethoxy)-HCID 44234674—
용매TetrahydrofuranHCID 8028—
생성물2-(Pyridin-4-yl)-1-(4-(quinolin-2-ylmethoxy)phenyl)ethan-1-oneHCID 3367972780%

반응 조건

온도-78 °C

반응 단계

To a solution of Lithium diisopropyl amide (1.0M) in tetrahydrofuran was added 4-picoline dropwise (7.55 ml, 5 eq.) at 0° C. under N2. After 30 min the anion was cooled to −78° C. In a separate round bottom flask N-Methoxy-N-methyl-4-(quinolin-2-ylmethoxy)-benzamide (5.0, 15.5 mmole) was dissolved in tetrahydrofuran (77 ml, 0.2M) and cooled to −78° C. under N2. 1.2 eq. of the 4-picoline anion was added dropwise to the amide solution. After 45 min, 1 eq. more of the 4-picoline anion was added. After an addition 30 min, acetic acid (40 ml) was added dropwise and the reaction was slowly warmed to ambient temperature. The solid product (acetate salt) was filtered and partitioned between saturated sodium bicarbonate and dichloromethane. The layers were separated, dried magnesium sulfate filtered and concentrated to provide the title compound as a tan solid (4.41 g, 80%). 1H NMR (400 MHz, CDCl3) δ 8.52 (d, J=5.8 Hz, 2 H), 8.19 (d, J=8.7 Hz, 1 H), 8.07 (d, J=8.7 Hz, 1H), 7.93 (m, 2 H), 7.82 (d, J=8.3 Hz, 1 H), 7.75 (m, 1 H), 7.61 (d, J=8.3 Hz, 1 H), 7.54 (dt, J=7.9, 1.0 Hz, 1 H), 7.23 (m, 2 H) 7.07 (m, 2H), 5.42 (s, 2H), 4.19 (s, 2H); MS: (M+H m/z=355.2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429665B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-fa627596c921474d9295989408bf324f
출처 메모uspto-grants-2008_09