Water → 5-Bromo-3-chloropyrazin-2-amine

HRID 81495

Reaktionsgleichung

Reaktionsgleichung von HRID 81495
[Cl:1][C:2]1[C:3]([NH2:8])=[N:4][CH:5]=[CH:6][N:7]=1.C(=O)([O-])[O-].[Na+].[Na+].[Br:15]Br.O>C(O)(=O)C>[Br:15][C:6]1[N:7]=[C:2]([Cl:1])[C:3]([NH2:8])=[N:4][CH:5]=1

Komponenten

6

Edukt 4

HCID 962WaterHCID 10340Sodium Carbonate2×HCID 24408Bromine2×HCID 2762242-Amino-3-chloropyrazine

Produkt 1

HCID 467382025-Bromo-3-chloropyrazin-2-amine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel3×

Versuchsvorschrift

3-Chloro-pyrazin-2-ylamine (0.750 g, 5.79 mmol) is suspended in acetic acid (7 ml) with stirring at room temperature and sodium carbonate (0.675 g, 6.37 mmol) is added. When all the gas has evolved bromine (0.171 ml, 3.34 mmol) in acetic acid (4 ml) is added dropwise. Sodium carbonate (0.675 g, 6.37 mmol) is added and a gas evolves. Once all gas has evolved bromine (0.171 ml, 3.34 mmol) in acetic acid (4 ml) is added. The reaction mixture is stirred at room temperature for 1 hour. The reaction mixture is poured onto iced water and left to stir for 30 minutes. A pale yellow suspension has formed. This solid is filtered off and rinsed with cold water to give 5-Bromo-3-chloro-pyrazin-2-ylamine.

Aufarbeitung

  1. additionis added dropwise
  2. additionis added
  3. stirringThe reaction mixture is stirred at room temperature for 1 hour
  4. waitleft
  5. stirringto stir for 30 minutes
  6. customA pale yellow suspension has formed
  7. filtrationThis solid is filtered off
  8. washrinsed with cold water

Quellen und Nachweise

ORD-Eintrag
ord-6070ba6a7f884eb59c1475f9ac09e9a1
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846687B2

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