HRID53163

反应详情

EQUATION

反应方程式

HRID 53163 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

0.75 g of 2-[4-(N,N-dimethylamino)-piperidino]-8-[N-benzyl-N-(3-aminopropyl)-amino]-4-morpholino-pyrimido[5,4-d]pyrimidine are dissolved in 8 ml of methylene chloride and mixed with 0.24 g of benzoyl chloride and 0.3 g of triethylamine in 2 ml of methylene chloride. The reaction mixture is stirred for 12 hours at ambient temperature and then extracted three times with water. The organic phase is dried over sodium sulphate and concentrated by rotary evaporation. The residue is chromatographed over a silica gel column using methylene chloride/methanol=7:3. Yield: 0.7 g (77% of theory) Oil C34H43N9O2 (609.78)

WORKUP

后处理

  1. extractionextracted three times with water
  2. dry with materialThe organic phase is dried over sodium sulphate
  3. concentrationconcentrated by rotary evaporation
  4. customThe residue is chromatographed over a silica gel column