HRID242135

反应详情

EQUATION

反应方程式

HRID 242135 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
10 °C

PROCEDURE

实验过程

A solution of 2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide (1 eq) and pyridine (4 eq) in MeCN (8 vol.) is heated to 70° C. A solution of methanesulfonic anhydride (1.5 eq) in MeCN (2 vol) is added over 50 min via addition funnel maintaining the temperature at less than 75° C. The mixture is stirred for an additional 0.5 hours after complete addition. The mixture is then allowed to cool to ambient. Ethanolamine (10 eq) is added via addition funnel. After stirring for 2 hours, water (6 vol.) is added and the mixture is cooled to 10° C. After stirring for NLT 3 hours, the solid is collected by filtration and washed with water (3 vat), 2:1 MeCN/water (3 vol), and MeCN (2×1.5 vol). The solid is dried to constant weight (<1% difference) in a vacuum oven at 50° C. with a slight N2 bleed to afford tert-butyl-3-(6-amino-3-methylpyridin-2-yl)benzoate as a red-yellow solid (53% yield).

WORKUP

后处理

  1. temperaturemaintaining the temperature at less than 75° C
  2. additionafter complete addition
  3. temperatureto cool to ambient
  4. stirringAfter stirring for 2 hours
  5. stirringAfter stirring for NLT 3 hours
  6. filtrationthe solid is collected by filtration
  7. washwashed with water (3 vat), 2:1 MeCN/water (3 vol), and MeCN (2×1.5 vol)
  8. dry with materialThe solid is dried to constant weight (<1% difference) in a vacuum oven at 50° C. with a slight N2