Bromine → 5-Bromo-4,6-dichloropyrimidin-2-amine

HRID 28567

Reaktionsgleichung

Reaktionsgleichung von HRID 28567
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([NH2:9])[N:3]=1.C([O-])(=O)C.[Na+].[Br:15]Br>C(O)(=O)C>[NH2:9][C:4]1[N:5]=[C:6]([Cl:8])[C:7]([Br:15])=[C:2]([Cl:1])[N:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a stirred mixture of 4,6-dichloro-pyrimidin-2-yl-amine (2.46 g, 15.0 mmol) and sodium acetate (6.15 g, 75.0 mmol) in acetic acid (150 ml) was added bromine (3.24 g, 20.25 mmol) dropwise. The mixture was then stirred at 60° C. for 2 hours. Volatiles were evaporated under reduced pressure. The residue was stirred with water (500 ml) for 1 hour, filtered, and dried under reduced pressure to provide 2-amino-4,6-dichloro-5-bromo-pyrimidine (3.2 g, 88% yield) as a white solid.

Aufarbeitung

  1. customVolatiles were evaporated under reduced pressure
  2. stirringThe residue was stirred with water (500 ml) for 1 hour
  3. filtrationfiltered
  4. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-16b556802db94a128af4492aaa101a92
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07419984B2

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