HRID63752

反应详情

EQUATION

反应方程式

HRID 63752 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a 200 mL flask containing (S)-2-[4-[[3,5-difluoro-4-[(S)-1-propoxycarbonyl-2-[4-[1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl]phenyl]ethylcarbamoyl]benzylamino]methyl]-2,6-difluorobenzoylamino]-3-[4-[1,3,6-trimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl]phenyl]propionic acid propyl ester (1004 mmg, 0.97 mmol) was added THF (25 mL), water (25 mL) and LiOH (193 mg, 4.6 mmol) and the reaction stirred at room temperature overnight. The reaction was concentrated, dried from acetonitrile yielding a white solid that was mixed with DMSO (13 mL) and water (12 mL). This mixture was heated minimally, filtered and to the filtrate was added TFA (0.25 mL) resulting in a precipitate. The precipitate was diluted with water (50 mL), filtered, washed with water and hexanes and dried on high vacuum yielding the title compound as a white solid (696 mg, 75%). ES(+)-LRMS m/e calcd. for C48H45F4N7O10 (M+H)+ 956, obsd 956.

WORKUP

后处理

  1. concentrationThe reaction was concentrated
  2. dry with materialdried from acetonitrile yielding a white solid that
  3. additionwas mixed with DMSO (13 mL) and water (12 mL)
  4. temperatureThis mixture was heated minimally
  5. filtrationfiltered and to the filtrate
  6. additionwas added TFA (0.25 mL)
  7. customresulting in a precipitate
  8. filtrationfiltered
  9. washwashed with water and hexanes
  10. customdried on high vacuum