HRID128634

反应详情

EQUATION

反应方程式

HRID 128634 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of ethyl 4-(4-methoxyanilino)-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylate (2.9 g) in dichloromethane (45 ml) was added rapidly to a suspension of powdered anhydrous aluminium chloride (12.8 g) in dichloromethane (115 ml) with stirring. The mixture was stirred for 24 hours at ambient temperature and then poured into ice/water. The mixture was stirred for 30 minutes then filtered. The residue was basified and partitioned between dichloromethane and water. The aqueous layer was evaporated to dryness. The residue was dissolved in propan-2-ol (150 ml) and then purified by column chromatography to give 6-hydroxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylic acid hemihydrate, m.p. 267°-268° C. (with decomposition).

WORKUP

后处理

  1. stirringThe mixture was stirred for 24 hours at ambient temperature
  2. stirringThe mixture was stirred for 30 minutes
  3. filtrationthen filtered
  4. custompartitioned between dichloromethane and water
  5. customThe aqueous layer was evaporated to dryness
  6. dissolutionThe residue was dissolved in propan-2-ol (150 ml)
  7. custompurified by column chromatography