Formamide → HCID 18409955, Verbindung

HRID 476590Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 476590
S(O)(O)(=O)=O.[NH2:6][C:7]1[N:8]=[C:9]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH2:22][CH2:23][CH3:24])[NH:10][C:11](=[O:14])[C:12]=1[NH2:13].S(=O)(=O)(O)O.[CH:30](N)=O>>[CH2:22]([O:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[C:9]1[N:8]=[C:7]2[C:12](=[N:13][CH:30]=[N:6]2)[C:11](=[O:14])[N:10]=1)[CH2:23][CH3:24]

Komponenten

4

Edukt 3

HCID 713FormamideHCID 1118Sulfuric AcidHCID 1363645694,5-Diamino-2-(propoxyphenyl)pyrimidin-6-one sulphate

Produkt 1

HCID 18409955HCID 18409955, Verbindung

Versuchsvorschrift

A stirred mixture of 4,5-diamino-2-(2-propoxyphenyl)pyrimidin-6-one sulphate (1.5 g) (prepared by the addition of concentrated sulphuric acid to an ethanolic solution of the free base) and formamide (15 ml) was heated in an oil bath (temp. 190°-200° C.) for 70 minutes. When cool the mixture was filtered and the collected solid was washed with ethanol to give a crude product (1.1 g), m.p. 254°-259° C., which was recrystallised from ethanol to give the title compound, 0.72 g, m.p. 263°-265° C.

Aufarbeitung

  1. temperaturewas heated in an oil bath (temp. 190°-200° C.) for 70 minutes
  2. temperatureWhen cool the mixture
  3. filtrationwas filtered
  4. washthe collected solid was washed with ethanol
  5. customto give a crude product (1.1 g), m.p. 254°-259° C., which
  6. customwas recrystallised from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-98875e5283ea47cd9992140358bd2d55
Quelldatensatz
uspto-grants-1989_12
Patentnummer
US04885301

Notizen zur Reaktion

Wird geladen…