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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1958664생성일: 2026년 10월 26일

Potassium Carbonate → methyl 2-(2-fluoro-5-((5-(6-methylpyridin-2-yl)-4-(quinolin-6-yl)-1H-imidazol-2-yl)methyl)phenoxy)acetate

https://huagongshe.com/reaction/1958664

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Methyl 3-chloropropionateHCID 22321—
반응물2-fluoro-5-((5-(6-methylpyridin-2-yl)-4-(quinolin-6-yl)-1H-imidazol-2-yl)methyl)phenolHCID 44546065—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물methyl 2-(2-fluoro-5-((5-(6-methylpyridin-2-yl)-4-(quinolin-6-yl)-1H-imidazol-2-yl)methyl)phenoxy)acetateHCID 4454600575.1%

반응 조건

온도60 °C

반응 단계

To a stirred solution of 2-fluoro-5-((5-(6-methylpyridin-2-yl)-4-(quinolin-6-yl)-1H-imidazol-2-yl)methyl)phenol (Example 81) (100 mg, 0.244 mmol) in acetone (5 mL) were added methyl 3-chloropropanoate (32 uL, 0.366 mmol) and K2CO3 (67 mg, 0.488 mmol) and the mixture was stirred at 60° C. for 20 hours. The reaction mixture was cooled to room temperature, diluted with H2O (20 mL), and extracted with CH2Cl2 (5 mL, 3 times). The organic layer was dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified by MPLC on NH silica gel (MeOH:CH2Cl2=1:50 (v/v)) to afford the title compound (88.4 mg, 75%). (300 MHz, CDCl3) δ 2.50 (3H, s), 3.74 (3H, s), 4.16 (2H, s), 4.71 (2H, s), 6.91-6.97 (3H, m), 7.06 (1H, td), 7.24 (1H, s), 7.37 (1H, d), 7.42 (1H, dd), 7.97 (1H, d), 8.10-8.18 (3H, m), 8.92 (1H, dd), 10.35 (1H, bs). MS (ESI) m/z 483 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410146B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-3464ccc23ccc42debfc220a9c37d94c6
출처 메모uspto-grants-2013_04