HRID1455747

反应详情

EQUATION

反应方程式

HRID 1455747 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a flask containing (1S)-(2,4-dichloro-6-methyl-pyrimidin-5-ylmethyl)methyl-(1,2,3,4-tetrahydro-naphthalen-1-yl)-amine (6.41 g, 19.06 mmol) is added MeOH (100 mL) and the solution is cooled to 0° C. using an ice bath. NaOMe (0.5 M, 38 mL) is added via addition funnel over 20 min. Once addition is complete, the ice bath is removed and the reaction is allowed to proceed overnight warming to room temperature. HOAc (2.0 mL) is added and the reaction mixture is allowed to stir for 10 min, followed by concentration at reduced pressure. The resulting oil is dissolved in EtOAc (100 mL) and washed sat. NaHCO3 (100 mL), brine (100 mL) and dried over Na2SO4. Flash chromatography on SiO2 using first CHCl3 followed by 20:1 hexanes:Et2O affords the title compound as a colorless oil. [mass expected (331.84); mass found (331.28)]

WORKUP

后处理

  1. additionOnce addition
  2. customthe ice bath is removed
  3. temperaturewarming to room temperature
  4. additionHOAc (2.0 mL) is added
  5. concentrationfollowed by concentration at reduced pressure
  6. dissolutionThe resulting oil is dissolved in EtOAc (100 mL)
  7. washwashed sat. NaHCO3 (100 mL), brine (100 mL)
  8. dry with materialdried over Na2SO4