Water → Aditeren

HRID 414518

Reaktionsgleichung

Reaktionsgleichung von HRID 414518
O.[NH2:2][C:3]1[N:8]=[C:7]([NH2:9])[C:6]([CH2:10][C:11]2[CH:16]=[C:15]([O:17][CH3:18])[C:14]([NH2:19])=[C:13]([O:20][CH3:21])[CH:12]=2)=[C:5](Cl)[N:4]=1>[Hg](Cl)Cl.[Zn].C(O)(=O)C>[NH2:2][C:3]1[N:8]=[C:7]([NH2:9])[C:6]([CH2:10][C:11]2[CH:12]=[C:13]([O:20][CH3:21])[C:14]([NH2:19])=[C:15]([O:17][CH3:18])[CH:16]=2)=[CH:5][N:4]=1

Komponenten

6

Versuchsvorschrift

A solution of 0.1 g. of mercury (II) chloride in 2 ml. of water and 1.5 g. of zinc powder was added to a solution of 1.5 g. of 2,4-diamino-5-(4-amino-3,5-dimethoxy-benzyl)-6-chloropyrimidine in 15.5 ml. of glacial acetic acid and the mixture was boiled under reflux with stirring overnight. Then, the mixture was filtered while hot and the zinc powder washed with 5 ml. of acetic acid. The combined filtrates were added dropwise with stirring at a temperature below 20° C. to 40 ml. of concentrated ammonia. Then, the mixture was stirred at 20° C. for an additional hour and the solid material was removed by filtration under vacuum, washed with water, dried, recrystallized from methanol and there was obtained 2,4-diamino-5-(4-amino-3,5-dimethoxy-benzyl)-pyrimidine having a melting point of 214° C.

Aufarbeitung

  1. temperatureunder reflux
  2. filtrationThen, the mixture was filtered while hot and the zinc powder
  3. washwashed with 5 ml
  4. additionThe combined filtrates were added dropwise
  5. stirringwith stirring at a temperature below 20° C. to 40 ml
  6. stirringThen, the mixture was stirred at 20° C. for an additional hour
  7. customthe solid material was removed by filtration under vacuum
  8. washwashed with water
  9. customdried
  10. customrecrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-eebeadb7cb424b44893b42416ee3cbff
Quelldatensatz
uspto-grants-1988_12
Patentnummer
US04792557

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