HRID1410831

反应详情

EQUATION

反应方程式

HRID 1410831 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 1-benzyl-5-hydroxy-2-oxo-3-phenyl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (60 mg, 0.16 mmol) and (2-amino-ethyl)-carbamic acid tert-butyl ester (75 mg, 0.47 mmol) was refluxed for 48 h. After cooling to r.t., AcOH (0.2 mL) was added, and the mixture was concentrated to dryness. The residue was dissolved in EtOAc and washed with 0.1 M HCl, saturated NaHCO3, and brine. The organic layer was dried over MgSO4 and concentrated to give 88 mg of the title compound as a pale yellow solid. MS: (+) m/z 515.30 (M+1).

WORKUP

后处理

  1. temperaturewas refluxed for 48 h
  2. concentrationthe mixture was concentrated to dryness
  3. dissolutionThe residue was dissolved in EtOAc
  4. washwashed with 0.1 M HCl, saturated NaHCO3, and brine
  5. dry with materialThe organic layer was dried over MgSO4
  6. concentrationconcentrated