HRID1623786

反应详情

EQUATION

反应方程式

HRID 1623786 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-[(Phenylmethyl)oxy]-N-3-pyridinyl-5-{[(2R)-2-pyrrolidinylmethyl]oxy}benzamide (may be prepared as described in Example 44; 250 mg, 0.62 mmol) was added to formic acid (4.5 ml) at 5° C., followed by 40% aqueous formaldehyde (2.4 ml). When the initial evolution of carbon dioxide had subsided, the mixture was refluxed for 2 h. After the solution was cooled, the pH of the solution was adjusted to 7-8 by adding aqueous NaHCO3 solution. The mixture was extracted with dichloromethane. The organic layer was dried over Na2SO4, and concentrated to obtain a crude product, which was purified by prep-HPLC to yield the title compound as a white solid. 47 mg.

WORKUP

后处理

  1. temperaturethe mixture was refluxed for 2 h
  2. temperatureAfter the solution was cooled
  3. extractionThe mixture was extracted with dichloromethane
  4. dry with materialThe organic layer was dried over Na2SO4
  5. concentrationconcentrated
  6. customto obtain a crude product, which
  7. customwas purified by prep-HPLC