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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Chloropyrimidine >  2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE

2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE

Basic information Safety Supplier Related

2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE Basic information

Product Name:
2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE
Synonyms:
  • 2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE
  • Quinazoline, 2,4-dichloro-5,6,7,8-tetrahydro-
CAS:
1127-85-1
MF:
C8H8Cl2N2
MW:
203.07
Mol File:
1127-85-1.mol
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2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE Chemical Properties

Melting point:
72-73 °C
Boiling point:
325.6±42.0 °C(Predicted)
Density 
1.385±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-1.77±0.20(Predicted)
Appearance
White to light yellow Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
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2,4-DICHLORO-5,6,7,8-TETRAHYDROQUINAZOLINE Usage And Synthesis

Synthesis

35042-48-9

1127-85-1

General procedure for the synthesis of 2,4-dichloro-5,6,7,8-tetrahydroquinazoline from 5,6,7,8-tetrahydroquinazoline-2,4(1H,3H)-dione: 5,6,7,8-tetrahydroquinazoline-2,4(1H,3H)-dione (8.0 g) was mixed with phosphorochloridic acid chloride (40 mL) and reacted at 120 °C for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and the excess phosphoryl chloride was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate (400 mL) and water (200 mL) for partitioning. The organic phase was washed sequentially with saturated NaHCO3 solution (200 mL) and brine (200 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography to afford 2,4-dichloro-5,6,7,8-tetrahydroquinazoline (4.0 g, 57% yield) as a yellow solid.1H NMR (400 MHz, CDCl3) δ 1.8 (br s, 4H), 2.73 (br s, 2H), 2.88 (br s, 2H).MS m/z (M+H): 203.1.

References

[1] Patent: WO2014/149164, 2014, A1. Location in patent: Paragraph 00688
[2] Journal of Medicinal Chemistry, 2011, vol. 54, # 2, p. 510 - 524

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