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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Chloropyridine >  6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE

6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE

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6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE Basic information

Product Name:
6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE
Synonyms:
  • 6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE
  • 6-Chloropyrido[3,4-d]pyrimidin-4(3H)-one
  • 6-CHLOROPYRIDO[3,4-D]PYRIMIDIN-4-OL
  • 6-Chloro-1H-pyrido[3,4-d]pyrimidin-4-one
  • 6-chloroPyrido[3,4-d]pyriMidin-4-one
  • 6-chloropyrido[3,4-d]pyrimidin-4(1H)-one
  • 6-Chloropyrido[3,4-d]pyrimidin-4(3H)
  • Pyrido[3,4-d]pyrimidin-4(3H)-one, 6-chloro-
CAS:
171178-47-5
MF:
C7H4ClN3O
MW:
181.58
EINECS:
604-604-1
Mol File:
171178-47-5.mol
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6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE Chemical Properties

Boiling point:
400.8±55.0 °C(Predicted)
Density 
1.66±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.26±0.20(Predicted)
Appearance
Light brown to brown Solid
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Safety Information

HS Code 
2933998090
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6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONE Usage And Synthesis

Synthesis

6313-33-3

58483-95-7

171178-47-5

5-Amino-2-chloropyridine-4-carboxylic acid (1000 g, 5.8 mol) and formamidine hydrochloride (1867 g, 23.2 mol) were mixed in ethylene glycol monomethyl ether (5000 mL) and sodium acetate (2360 g, 17.4 mol) was added. The reaction mixture was heated to 120 °C and maintained at this temperature for 6 hours. After completion of the reaction, it was cooled to room temperature and the reaction solution was poured into water (4000 mL) and extracted twice with ethyl acetate. The organic phases were combined, dried and concentrated to give the crude product. The crude product was filtered to give 6-chloropyrido[3,4-d]pyrimidin-4(3H)-one (924 g, 5.1 mol).

References

[1] Patent: CN104130256, 2016, B. Location in patent: Paragraph 0027; 0028; 0030

6-CHLORO-3H-PYRIDO[3,4-D]PYRIMIDIN-4-ONESupplier

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