Benzyl Bromide → 7-Benzyl-3-methylxanthine

HRID 323850

Reaktionsgleichung

Reaktionsgleichung von HRID 323850
[OH-].[Na+].[CH3:3][N:4]1[C:12]2[N:11]=[CH:10][NH:9][C:8]=2[C:7](=[O:13])[NH:6][C:5]1=[O:14].[CH2:15](Br)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>O.CO>[CH2:15]([N:9]1[C:8]2[C:7](=[O:13])[NH:6][C:5](=[O:14])[N:4]([CH3:3])[C:12]=2[N:11]=[CH:10]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

20 g (0.5 mol) of sodium hydroxide dissolved in 200 ml of water were added to a suspension of 83 g (0.5 mol) of 3-methylxanthine in 500 ml of methanol and the reaction mixture was stirred at 70° C. for one hour, then treated dropwise at the same temperature with 85.5 g (0.5 mol) of benzyl bromide and kept between 700 and 800 for 5 hours. The mixture was then cooled and filtered cold on a suction filter, the product was washed with water on the suction filter and dissolved hot in 1000 ml of 1N sodium hydroxide solution, filtered and slowly brought to pH 9.5 using 4N hydrochloric acid with stirring. The crystallizate was filtered off from the still warm solution, washed with water until chloride-free and dried in a vacuum drying oven overnight. Yield: 81.7 g (63.8% of theory); melting point: 263° C. C13H12N4O2 (MW=256.2 g/mol)

Aufarbeitung

  1. waitkept between 700 and 800 for 5 hours
  2. temperatureThe mixture was then cooled
  3. filtrationfiltered cold on a suction
  4. filtrationfilter
  5. washthe product was washed with water on the suction
  6. filtrationfilter
  7. dissolutiondissolved hot in 1000 ml of 1N sodium hydroxide solution
  8. filtrationfiltered
  9. stirringwith stirring
  10. filtrationThe crystallizate was filtered off from the still warm solution
  11. washwashed with water until chloride-free
  12. customdried in a vacuum
  13. customdrying oven overnight

Quellen und Nachweise

ORD-Eintrag
ord-509c10c13d0b40d4b4693ae8e2b6aa3f
Quelldatensatz
uspto-grants-2001_04
Patentnummer
US06214992B1

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