HRID1751421

反应详情

EQUATION

反应方程式

HRID 1751421 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Methyl (S)-1-((S)-2-(5-(6-(2-((S)-1-((R)-2-methoxycarbonylamino-2-phenylacetyl)pyrrolidin-2-yl)-4,5-dihydro-1H-naphtho[1,2-d]imidazol-7-yl)naphthalen-2-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamate (150 mg, 0.178 mmol) was dissolved in DCM (9 mL) and MnO2 (155 mg, 1.78 mmol) was added. After stirring for 16.5 h, more MnO2 (619 mg, 7.12 mmol) was added and the reaction mixture was heated to reflux. 1.5 h later, 9 mL DCM were added and MnO2 (619 mg, 7.12 mmol) was added. After another 4 h, MnO2 (619 mg, 7.12 mmol) was added. After and additional 16 h, the reaction mixture was filtered over celite and concentrated. The crude residue was purified by HPLC to afford the title compound (42 mg, 29%). MS (ESI) m/z 847 [M+H]+.

WORKUP

后处理

  1. temperaturethe reaction mixture was heated to reflux
  2. waitAfter another 4 h
  3. filtrationAfter and additional 16 h, the reaction mixture was filtered over celite and
  4. concentrationconcentrated
  5. customThe crude residue was purified by HPLC