HRID2414176

反应详情

EQUATION

反应方程式

HRID 2414176 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a well stirred solution of 1.16 g of 9-methoxy-4-methyl-2,3,4a,5-tetrahydro-4H-[1]-benzopyrano[3,4-b]pyridine in 15 ml of THF is added 3.4 ml of 1.5M butyl lithium in hexane at 0°. After 5 minutes at 0°, the reaction mixture is cooled to -70° and 0.6 ml of t-butyl isocyanate is added. After warming to room temperature the reaction mixture is diluted with water and the products extracted with ether. After drying over magnesium sulfate, the solvent is removed in vacuo and the residue is crystallized from ether/hexane to yield cis-2-(N-t-butylcarbamoyl)-9-methoxy-4-methyl-2,3,4a,5,-tetrahydro-4H-[1]-benzopyrano[3,4-b]pyridine, which is converted wiht ethanolic hydrogen chloride to cis-2-(N-t-butylcarbamoyl)-9-methoxy-4-methyl-2,3,4a,5-tetrahydro-4H-[1]-benzopyrano[3,4-b]pyridine hydrochloride, melting point 188°-189° (from ethanol/ether).

WORKUP

后处理

  1. temperaturethe reaction mixture is cooled to -70°
  2. extractionthe products extracted with ether
  3. dry with materialAfter drying over magnesium sulfate
  4. customthe solvent is removed in vacuo
  5. customthe residue is crystallized from ether/hexane