HRID1199530

反应详情

EQUATION

反应方程式

HRID 1199530 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Phosphorus pentachloride (1.0 g) was added to a stirred solution of 6-acetamido-2-methoxy-8-methylquinoline (1.0 g) in toluene (50 cm3) and the mixture was stirred at 50° for 15 minutes. Acetyl hydrazine (1.35 g) was then added and the mixture was stirred for 3 hours at 60°. The toluene was removed in vacuo the residue dissolved in ethanol, and aqueous ammonia solution (S.G. 0.88) (25 cm3) was added. Dichloromethane (100 cm3) was added and the organic phase was separated. The aqueous phase was further extracted with dichloromethane (2×25 cm3), and the combined organic phases were dried (MgSO4) and evaporated to give a solution which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with dichloromethane:methanol, 19:1. Combination and evaporation of appropriate fractions afforded 6-[3,5-dimethyl-1,2,4-triazol-4-yl]-2-methoxy-8-methylquinoline (0.306 g), which was recrystallised from toluene to give microcrystals, m.p. 211°-213° (0.066 g).

WORKUP

后处理

  1. stirringthe mixture was stirred for 3 hours at 60°
  2. customThe toluene was removed in vacuo the residue
  3. dissolutiondissolved in ethanol
  4. additionaqueous ammonia solution (S.G. 0.88) (25 cm3) was added
  5. additionDichloromethane (100 cm3) was added
  6. customthe organic phase was separated
  7. extractionThe aqueous phase was further extracted with dichloromethane (2×25 cm3)
  8. dry with materialthe combined organic phases were dried (MgSO4)
  9. customevaporated
  10. customto give a solution which
  11. customwas chromatographed on silica (Merck "MK 60.9385" [Trade Mark])
  12. washeluting with dichloromethane
  13. customCombination and evaporation of appropriate fractions