HRID542838

反应详情

EQUATION

反应方程式

HRID 542838 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 3 g (0.008 mole) of 6-methoxy-4-methyl-N-[6-(1-piperazinyl)hexyl]-8-quinolinamine (Example 1) and 0.72 ml (0.008 mole) of 3-chloro-1,2-propanediol was heated at 120° for 2 hours. An additional 0.2 ml of 3-chloro-1,2-propanediol and 1 ml of triethylamine were added and the mixture was heated at 130° for 3 hr and allowed to cool. The reaction mixture was diluted with ethyl acetate, washed with water and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated to dryness in vacuo. The residual oil was chromatographed over 200 g of silica gel, eluting first with one liter of a 1:15:84 mixture of triethylamine:methanol:ethyl acetate and then with a 1:20:79 mixture of the same solvents. That portion of the eluant containing fairly pure product Rf (silica--25 parts of methanol:75 parts of ethyl acetate:1 part of triethylamine)=0.26 was concentrated to dryness, taken up in 2-propanol and treated with an excess of a 17% solution of hydrogen chloride in 2-propanol to afford 0.7 g of product. That portion of the eluant containing contaminated product was concentrated and rechromatographed over 50 g of silica with a 1:15:84 mixture of triethyl amine:methanol:ethyl acetate and the product was isolated as described above. The two crops were combined and recrystallized from ethanol to afford 1.0 g (23%) of the title compound, mp. 237°-241° (dec) with prior sintering.

WORKUP

后处理

  1. temperaturewas heated at 120° for 2 hours
  2. temperaturethe mixture was heated at 130° for 3 hr
  3. temperatureto cool
  4. washwashed with water and saturated sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness in vacuo
  8. customThe residual oil was chromatographed over 200 g of silica gel
  9. washeluting first with one liter of a 1:15:84 mixture of triethylamine
  10. additionmethanol:ethyl acetate and then with a 1:20:79 mixture of the same solvents
  11. additionThat portion of the eluant containing fairly pure product Rf (silica--25 parts of methanol:75 parts of ethyl acetate:1 part of triethylamine)=0.26
  12. concentrationwas concentrated to dryness
  13. additiontreated with an excess of a 17% solution of hydrogen chloride in 2-propanol