HRID562735

反应详情

EQUATION

反应方程式

HRID 562735 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

9-(5-Chloropentyl)-2-{[(1S)-1-methylbutyl]oxy}-8-(methyloxy)-9H-purin-6-amine (80 mg, 0.225 mmol), triethylamine (0.031 ml, 0.225 mmol) and piperidine (0.045 ml, 0.45 mmol) were suspended in DMF (3 ml) and the mixture heated to 70° C. for 18 hours. The solvent was removed and the residue partitioned between DCM (4 ml) and saturated sodium bicarbonate (4 ml). The aqueous phase was re-extracted with further DCM and the combined organic extracts were concentrated and the residue dissolved in 1:1 MeOH:DMSO (1 ml) and purified by MDAP (Method A). The product-containing fractions were combined and evaporated under a stream of nitrogen to give the title compound (47.2 mg).

WORKUP

后处理

  1. customThe solvent was removed
  2. customthe residue partitioned between DCM (4 ml) and saturated sodium bicarbonate (4 ml)
  3. extractionThe aqueous phase was re-extracted with further DCM
  4. concentrationthe combined organic extracts were concentrated
  5. dissolutionthe residue dissolved in 1:1 MeOH
  6. customDMSO (1 ml) and purified by MDAP (Method A)
  7. customevaporated under a stream of nitrogen