反应 #1702176

反应方程式

tetrahydrofuran

racemic 3-bromo 4,5-dihydroisoxazole

5-hydroxynicotinic acid methyl ester

lithium hydroxide

→

3-(pyridin-3-yloxy)-4,5-dihydroisoxazole

溶剂

tetrahydrofuran water

反应条件

后处理

1. 1
   workup.ADDITIONwas added
2. 2
   其他was removed under a stream of nitrogen

实验过程

The enantiomers of 3-(pyridin-3-yloxy)-4,5-dihydroisoxazole III-74a and III-74b were prepared in 2 steps according to the following procedures: racemic 3-bromo 4,5-dihydroisoxazole III-66 was reacted with 5-hydroxynicotinic acid methyl ester using Method 5. The resulting ester (1.0 equiv) was dissolved in 1:1 tetrahydrofuran/water (0.06 M) and lithium hydroxide (8.0 equiv) was added. The reaction was allowed to stir at room temperature for 1 h after which point the tetrahydrofuran was removed under a stream of nitrogen and the remaining solution was acidified to pH<2 with 1N HCl to provide the racemic desired acid III-74 as a white solid which was isolated via vacuum filtration. These compounds can be separated using chiral HPLC methods known in the art. For example, see chiral HPLC Method disclosed herein. [M+H]+=395.5 m/z. Activity: A

来源