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6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONE

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6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONE Basic information

Product Name:
6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONE
Synonyms:
  • 6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONE
  • 6-BroMo-3H-pyrido[2,3-d]p...
  • 6-BroMo-3H-pyrido[2,3-d]pyriMidin-4-one
  • 6-bromo-3H,4H-pyrido[2,3-d]pyrimidin-4-one
  • 6-bromopyrido[2,3-d]pyrimidin-4(3H)-one
  • 6-Bromo-1H-pyrido[2,3-d]pyrimidin-4-one
  • 6-Bromopyrido[2,3-d]pyrimidin-4(1H)
  • Pyrido[2,3-d]pyrimidin-4(3H)-one, 6-bromo-
CAS:
155690-79-2
MF:
C7H4BrN3O
MW:
226.03
Mol File:
155690-79-2.mol
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6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONE Chemical Properties

Boiling point:
455.3±30.0 °C(Predicted)
Density 
2.01±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
9.20±0.20(Predicted)
Appearance
Light yellow to yellow Solid
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6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONE Usage And Synthesis

Synthesis

3473-63-0

5794-88-7

155690-79-2

The general procedure for the synthesis of 6-bromopyrido[2,3-d]pyrimidin-4(1H)-ones from formamidine acetate and 2-amino-5-bromobenzoic acid was as follows: formamidine acetate (1 eq.) was added to a 1.2 M solution of 2-amino-5-bromobenzoic acid (1 eq.) in N,N-dimethylformamide. The reaction mixture was heated to reflux and stirred at this temperature for 16 hours. Upon completion of the reaction, the mixture was cooled to room temperature, followed by the slow addition of a 5% aqueous NaHCO3 solution (3 volumes) with vigorous stirring. The resulting precipitate was collected by filtration and washed sequentially with water (2 x 1 volume) and tert-butyl methyl ether (2 x 1 volume). Finally, the product was dried in a vacuum oven to afford 6-bromopyrido[2,3-d]pyrimidin-4(1H)-one without further purification. The product yield was 91% and LC-MS analysis showed m/z of 225 [M-H]? and retention time of 2.31 min.

References

[1] Patent: WO2008/23161, 2008, A1. Location in patent: Page/Page column 111-112

6-BROMOPYRIDO[2,3-D]PYRIMIDIN-4(1H)-ONESupplier

NovoChemy Ltd.
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Shanghai Rong Lin Medical Technology Co., Ltd.
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