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Methanol → 2-Amino-5-chloro-3-methoxypyrazine

HRID 1107467
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1107467
[Na].[NH2:2][C:3]1[C:8](Br)=[N:7][C:6]([Cl:10])=[CH:5][N:4]=1.[OH2:11].[CH3:12]O>>[NH2:2][C:3]1[C:8]([O:11][CH3:12])=[N:7][C:6]([Cl:10])=[CH:5][N:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 887MethanolHCID 962WaterHCID 5360545SodiumHCID 104886093-Bromo-5-chloropyrazin-2-amine

Produkt 1

HCID 107970362-Amino-5-chloro-3-methoxypyrazine

Versuchsvorschrift

Sodium (2.82 g) was dissolved in dry methanol (50 ml) under argon and 2-amino-3-bromo-5-chloropyrazine (1.68 g) was added in small portions with stirring. The stirred solution was heated at reflux under an atmosphere of argon for 4 hours. The solution was allowed to cool to ambient temperature and water (10 ml) was added. Volatile material was removed by evaporation and water (10 ml) was added to the residue. The mixture was extracted with dichloromethane (3×50 ml) and the combined extracts were dried (MgSO4) and evaporated to give 2-amino-5-chloro-3-methoxypyrazine (1.28 g), m.p. 102-103° C.; 1H NMR (d6 -DMSO): 3.90 (s, 3H), 7.53 (s, 1H); mass spectrum (+ve CI): 160 (M+H)+.

Aufarbeitung

  1. temperatureThe stirred solution was heated
  2. temperatureat reflux under an atmosphere of argon for 4 hours
  3. customVolatile material was removed by evaporation and water (10 ml)
  4. additionwas added to the residue
  5. extractionThe mixture was extracted with dichloromethane (3×50 ml)
  6. dry with materialthe combined extracts were dried (MgSO4)
  7. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-08e1b076b4574af89cff437f058b09bf
Quelldatensatz
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06060475

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