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Methyl iodide → 2-Amino-3-methyl-6-phenyl-4-pyrimidinone

HRID 1785440
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1785440
[OH-].[K+].[CH3:3]I.[NH2:5][C:6]1[NH:11][C:10](=[O:12])[CH:9]=[C:8]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:7]=1>CCO>[NH2:5][C:6]1[N:11]([CH3:3])[C:10](=[O:12])[CH:9]=[C:8]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6328Methyl iodide2×HCID 14797Potassium HydroxideHCID 1354203652-Amino-6-phenylpyrimidin-4-ol

Produkt 1

HCID 133205052-Amino-3-methyl-6-phenyl-4-pyrimidinone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A mixture of KOH (1.22 g, 22 mmol), MeI (6.85 g, 48 mmol), and 2-amino-6-phenyl-3H-pyrimidin-4-one (2.62 g, 14 mmol) in EtOH (130 mL) was stirred at room temperature in a stoppered 250 mL roundbottom flask for 3 days. An additional 6.85 g (48 mmol) MeI was added and stirring was continued for 1 day. The solvent was removed under vacuum and the residue was dissolved in H2O (35mL), warmed to 50° C., and 1N HCl was added dropwise until the solid dissolved completely. The solution was cooled to room temperature, made slightly basic with saturated NaHCO3, and the resulting white solid was filtered and dried under vacuum. M+1: 202.

Aufarbeitung

  1. stirringstirring
  2. waitwas continued for 1 day
  3. customThe solvent was removed under vacuum
  4. dissolutionthe residue was dissolved in H2O (35mL)
  5. temperaturewarmed to 50° C.
  6. addition1N HCl was added dropwise until the solid
  7. dissolutiondissolved completely
  8. temperatureThe solution was cooled to room temperature
  9. filtrationthe resulting white solid was filtered
  10. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-39cb08f716ea46fc9d7265a15ce12e7a
Quelldatensatz
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07504403B2

Notizen zur Reaktion

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