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