HRID1977220

反应详情

EQUATION

反应方程式

HRID 1977220 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

7-Chloro-4-hydroxy-2-(4-methoxy-2-methylphenyl)-1,2,5,10-tetrahydropyridazino-[4,5-b]quinoline-1,10-dione (0.45 g, 1.17 mM) was stirred in methanol (20 mL) and N-Methyl-D-Glucamine (0.23 g, 1.17 mM) was added to give a clear yellow solution. This solution was concentrated and the residue was dissolved in water (20 mL) to give a yellow solution. This solution was filtered through a Gellman 0.45 um Acrodisc and concentrated to give a yellow residue. The residue was triturated with 2-propanol (20 mL) to give a yellow suspension. The solids were collected and washed with 2-propanol to give the title compound (0.20 g, 29%) as a yellow powder, mp=177 C (decomp.).

WORKUP

后处理

  1. customto give a clear yellow solution
  2. concentrationThis solution was concentrated
  3. dissolutionthe residue was dissolved in water (20 mL)
  4. customto give a yellow solution
  5. filtrationThis solution was filtered through a Gellman 0.45 um Acrodisc
  6. concentrationconcentrated
  7. customto give a yellow residue
  8. customThe residue was triturated with 2-propanol (20 mL)
  9. customto give a yellow suspension
  10. customThe solids were collected
  11. washwashed with 2-propanol