HRID1977220
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- customto give a clear yellow solution
- concentrationThis solution was concentrated
- dissolutionthe residue was dissolved in water (20 mL)
- customto give a yellow solution
- filtrationThis solution was filtered through a Gellman 0.45 um Acrodisc
- concentrationconcentrated
- customto give a yellow residue
- customThe residue was triturated with 2-propanol (20 mL)
- customto give a yellow suspension
- customThe solids were collected
- washwashed with 2-propanol