HRID1489671

反应详情

EQUATION

反应方程式

HRID 1489671 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Alternatively, a suspension of 3-cyclopentyloxy-4-methoxybenzamide (2.58 g; that is prepared as described in Reference Example 73) in dry toluene (40 mL) is heated at reflux and treated with potassium t-butoxide (1.4 g), followed by 3,4,5-trichloro-pyridine (1.82 g). The mixture is then heated at reflux for 3 hours and 45 minutes, and is then treated with a further quantity of potassium t-butoxide (1.4 g) and heated at reflux for a further period of 7 hours. The mixture is allowed to cool and is then filtered. The filtrate is evaporated and the resulting residue is extracted with aqueous sodium hydroxide solution (2M). The alkaline solution is then acidified by treatment with acetic acid, and the solid which separates is collected by filtration, washed with water and dried, to give N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methoxybenzamide (2.09 g) in the form of a buff solid, m.p. 153°-155° C.

WORKUP

后处理

  1. customthat is prepared
  2. temperatureis heated
  3. temperatureat reflux
  4. temperatureThe mixture is then heated
  5. temperatureat reflux for 3 hours and 45 minutes
  6. temperatureheated
  7. temperatureat reflux for a further period of 7 hours
  8. temperatureto cool
  9. filtrationis then filtered
  10. customThe filtrate is evaporated
  11. extractionthe resulting residue is extracted with aqueous sodium hydroxide solution (2M)
  12. filtrationthe solid which separates is collected by filtration
  13. washwashed with water
  14. customdried