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2,4-Dichloropyrido[2,3-d]pyrimidine

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2,4-Dichloropyrido[2,3-d]pyrimidine Basic information

Product Name:
2,4-Dichloropyrido[2,3-d]pyrimidine
Synonyms:
  • 2,4-dichloropyrido[2,3-d]...
  • Pyrido[2,3-d]pyrimidine,2,4-dichloro-
  • 2,4-DICHLOROPYRIDO[2,3-D]PYRIMIDINE
  • 2,4-Dichloro-pyrido[2,3-d]pyrimidine2,4-Dichloro-pyrido[2,3-d]pyrimidine
CAS:
126728-20-9
MF:
C7H3Cl2N3
MW:
200.02
Mol File:
126728-20-9.mol
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2,4-Dichloropyrido[2,3-d]pyrimidine Chemical Properties

Melting point:
157-158 °C (decomp)
Density 
1.573±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-0.38±0.30(Predicted)
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2,4-Dichloropyrido[2,3-d]pyrimidine Usage And Synthesis

Reactivity Profile

Selective disubstitution of 2,4-dichloropyrido[2,3-d]pyrimidine with various nucleophiles was investigated by Lavecchia et al. Suzuki and Stille cross-coupling reactions on monosubstituted compound 4-tert-butylamino-2-chloro-pyrido[2,3-d]pyrimidine were performed in high yields. ,4-dichloropyrido[2,3-d]pyrimidine was easily substituted at position 4 with different nucleophiles. This position was more reactive than position 2, as in simple pyrimidinic systems. 2,4-dichloropyrido[2,3-d]pyrimidine 3 was prepared from 2-aminonicotinic acid 1 via 2,4-dihydroxypyrido[2,3-d]pyrimidine 2 following Robin and Hitchings method.

Synthesis

2,4-dichloropyrido[2,3-d]pyrimidine 3 was prepared from 2-aminonicotinic acid 1 via 2,4-dihydroxypyrido[2,3-d]pyrimidine 2 following Robin and Hitchings method[1].

References

[1] G. Lavecchia, G. Guillaumet, S. Berteina-Raboin. “Selective bifunctionalization of pyrido[2,3-d]pyrimidines in positions 2 and 4 by SNAr and palladium-catalyzed coupling reactions.” Tetrahedron Letters 46 35 (2005): Pages 5851-5855.

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