HRID1011182

反应详情

EQUATION

反应方程式

HRID 1011182 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of 2-(2-ethoxyethoxy)-8-methoxy-9-(tetrahydro-2H-pyran-3-ylmethyl)-9H-purin-6-amine (245 mg) in dry methanol (10 ml) at room temperature and under nitrogen was added 4.0M hydrogen chloride in 1,4-dioxane (4.0 ml). The reaction was left to stir at room temperature for 1 hour. The reaction was concentrated in vacuo and the resulting residue purified by C18 reverse phase chromatography using water (containing 0.1% formic acid)-acetonitrile (containing 0.05% formic acid) as eluant (10-45%) to afford a white solid. This was taken up in water (15 ml) and neutralised by the addition of 2.0M sodium hydroxide solution. The solid was filtered and dried on the rotary evaporator (60° C.) for 30 minutes (90 mg).

WORKUP

后处理

  1. waitThe reaction was left
  2. concentrationThe reaction was concentrated in vacuo
  3. customthe resulting residue purified by C18 reverse phase chromatography
  4. customto afford a white solid
  5. filtrationThe solid was filtered
  6. customdried on the rotary evaporator (60° C.) for 30 minutes (90 mg)