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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Methylpyrimidine >  2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE

2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE

Basic information Safety Supplier Related

2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE Basic information

Product Name:
2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE
Synonyms:
  • 2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE
  • 2,4-Dichloro-5H,6H,7H-cyclopenta[d]pyrimidine
  • 2,4-Dichloro-5,6-trimethylenepyrimidine
  • 4-dichloro-6
  • 7-dihydro-5H-cyclopenta[d]pyriMidine
  • 2,4-dichloro-6,7-dihydro-5H-cyclopenta[d][1,3]chlorazine
  • EOS-60937
  • 5H-Cyclopentapyrimidine, 2,4-dichloro-6,7-dihydro-
CAS:
5466-43-3
MF:
C7H6Cl2N2
MW:
189.04
Product Categories:
  • Heterocycle-Pyrimidine series
Mol File:
5466-43-3.mol
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2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE Chemical Properties

Melting point:
70-72℃
Boiling point:
307℃
Density 
1.466
Flash point:
168℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-1.78±0.20(Predicted)
Appearance
Off-white to light yellow Solid
InChIKey
GDHHAOFBLGZCMI-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933599590
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2,4-DICHLORO-6,7-DIHYDRO-5H-CYCLOPENTAPYRIMIDINE Usage And Synthesis

Synthesis

5466-00-2

5466-43-3

General procedure for the synthesis of 2,4-dichloro-5,6-trimethylpyrimidine from 6,7-dihydro-1H-cyclopenta[d]pyrimidine-2,4(3H,5H)-dione: 6,7-dihydro-1H-cyclopenta[d]pyrimidine-2,4(3H,5H)-dione (0.3 g, 1.97 mmol) was suspended in phosphorochloridic acid (5 ml) and heated to reflux overnight. Upon completion of the reaction, the reaction mixture was cooled to room temperature followed by slow addition of water under ice bath conditions. The precipitated product was collected by filtration and dried to give 2,4-dichloro-5,6-trimethylpyrimidine as a yellow solid. Yield: 92%. 1H NMR (DMSO-d6, 300 MHz): δ 3.13 (t, 2H, cyclopentyl-CH2), 3.00 (t, 2H, cyclopentyl-CH2), 2.23 (m, 2H, cyclopentyl-CH2).

References

[1] European Journal of Medicinal Chemistry, 1980, vol. 15, # 4, p. 317 - 322
[2] European Journal of Medicinal Chemistry, 2015, vol. 92, p. 246 - 256
[3] Patent: US2010/144731, 2010, A1. Location in patent: Page/Page column 22
[4] Patent: US2007/281949, 2007, A1. Location in patent: Page/Page column 93-94
[5] Patent: US2014/179668, 2014, A1. Location in patent: Paragraph 0829

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