HRID2370863

反应详情

EQUATION

反应方程式

HRID 2370863 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of (S)-methyl 6-(((3-fluoro-4-(trifluoromethoxy)phenyl)(3-fluoropyridin-2-yl)methyl)carbamoyl)nicotinate (11.5 g, 24.61 mmol) in MeOH (140 mL, Aldrich) was added lithium hydroxide hydrate (2.065 g, 49.2 mmol, Aldrich). The mixture was stirred at room temperature for 5 min followed by the addition of THF (5 mL, Aldrich) and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo, cooled to 0° C. and was adjusted to pH=6-7 with concentrated HCl. EtOAc (300 mL) was added to the adjusted pH mixture, and the resulting mixture was stirred at room temperature for 15 min. The organic layer was collected and the aqueous phase was extracted with EtOAc (1×200 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo. The residue was then dissolved in MeOH (400 mL) and silica gel was added. The mixture was concentrated and dried in vacuo. The solid mixture was then purified by silica gel flash column chromatography using ISCO instrument (solid loading, 40% EtOAc/hexane, then 10% MeOH in EtOAc) to give the title compound as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 13.75 (br. s., 1H), 9.85 (d, J=7.4 Hz, 1H), 9.18 (d, J=1.4 Hz, 1H), 8.58 (d, J=4.7 Hz, 1H), 8.48 (dd, J=8.1, 2.1 Hz, 1H), 8.16 (d, J=8.0 Hz, 1H), 7.83 (t, J=9.3 Hz, 1H), 7.50-7.61 (m, 3H), 7.36 (d, J=8.4 Hz, 1H), 6.58 (d, J=7.2 Hz, 1H). MS (ESI, positive ion) m/z: 454.0 (M+H)

WORKUP

后处理

  1. stirringthe mixture was stirred at room temperature for 1 h
  2. concentrationThe mixture was concentrated in vacuo
  3. temperaturecooled to 0° C.
  4. additionEtOAc (300 mL) was added to the adjusted pH mixture
  5. stirringthe resulting mixture was stirred at room temperature for 15 min
  6. customThe organic layer was collected
  7. extractionthe aqueous phase was extracted with EtOAc (1×200 mL)
  8. dry with materialThe combined organic layers were dried over MgSO4
  9. concentrationconcentrated in vacuo
  10. dissolutionThe residue was then dissolved in MeOH (400 mL)
  11. additionsilica gel was added
  12. concentrationThe mixture was concentrated
  13. customdried in vacuo
  14. customThe solid mixture was then purified by silica gel flash column chromatography