Pyrimidine

Not to be confused with Pyridine.
Pyrimidine
Pyrimidine molecule
Pyrimidine molecule
Names
Preferred IUPAC name
Pyrimidine[1]
Other names
1,3-Diazine
m-Diazine
Identifiers
289-95-2 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:16898 YesY
ChEMBL ChEMBL15562 YesY
ChemSpider 8903 YesY
ECHA InfoCard 100.005.479
KEGG C00396 YesY
MeSH pyrimidine
PubChem 9260
Properties
C4H4N2
Molar mass 80.088 g mol−1
Density 1.016 g cm−3
Melting point 20 to 22 °C (68 to 72 °F; 293 to 295 K)
Boiling point 123 to 124 °C (253 to 255 °F; 396 to 397 K)
Acidity (pKa) 1.10[2] (protonated pyrimidine)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine.[3] One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogen atoms at positions 1 and 3 in the ring.[4]:250 The other diazines are pyrazine (nitrogen atoms at the 1 and 4 positions) and pyridazine (nitrogen atoms at the 1 and 2 positions). In nucleic acids, three types of nucleobases are pyrimidine derivatives: cytosine (C), thymine (T), and uracil (U).

Occurrence and history

Pinner's 1885 structure for pyrimidine

The pyrimidine ring system has wide occurrence in nature[5] as substituted and ring fused compounds and derivatives, including the nucleotides, thiamine (vitamin B1) and alloxan. It is also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. Although pyrimidine derivatives such as uric acid and alloxan were known in the early 19th century, a laboratory synthesis of a pyrimidine was not carried out until 1879,[5] when Grimaux reported the preparation of barbituric acid from Ivy urea and malonic acid in the presence of phosphorus oxychloride.[6] The systematic study of pyrimidines began[7] in 1884 with Pinner,[8] who synthesized derivatives by condensing ethyl acetoacetate with amidines. Pinner first proposed the name “pyrimidin” in 1885.[9] The parent compound was first prepared by Gabriel and Colman in 1900,[10] [11] by conversion of barbituric acid to 2,4,6-trichloropyrimidine followed by reduction using zinc dust in hot water.

Nomenclature

The nomenclature of pyrimidines is straightforward. However, like other heterocyclics, tautomeric hydroxyl groups yield complications since they exist primarily in the cyclic amide form. For example, 2-hydroxypyrimidine is more properly named 2-pyrimidone. A partial list of trivial names of various pyrimidines exists.[12]:5–6

Physical properties

Physical properties are shown in the data box. A more extensive discussion, including spectra, can be found in Brown et al.[12]:242–244

Chemical properties

Per the classification by Albert[13]:56–62 six-membered heterocycles can be described as π-deficient. Substitution by electronegative groups or additional nitrogen atoms in the ring significantly increase the π-deficiency. These effects also decrease the basicity.[13]:437–439

Like pyridines, in pyrimidines the π-electron density is decreased to an even greater extent. Therefore, electrophilic aromatic substitution is more difficult while nucleophilic aromatic substitution is facilitated. An example of the last reaction type is the displacement of the amino group in 2-aminopyrimidine by chlorine[14] and its reverse.[15]

Electron lone pair availability (basicity) is decreased compared to pyridine. Compared to pyridine, N-alkylation and N-oxidation are more difficult. The pKa value for protonated pyrimidine is 1.23 compared to 5.30 for pyridine. Protonation and other electrophilic additions will occur at only one nitrogen due to further deactivation by the second nitrogen.[4]:250 The 2-, 4-, and 6- positions on the pyrimidine ring are electron deficient analogous to those in pyridine and nitro- and dinitrobenzene. The 5-position is less electron deficient and substitutents there are quite stable. However, electrophilic substitution is relatively facile at the 5-position, including nitration and halogenation.[12]:4–8

Reduction in resonance stabilization of pyrimidines may lead to addition and ring cleavage reactions rather than substitutions. One such manifestation is observed in the Dimroth rearrangement.

Pyrimidine is also found in meteorites, but scientists still do not know its origin. Pyrimidine also photolytically decomposes into uracil under ultraviolet light.[16]

Synthesis

As is often the case with parent heterocyclic ring systems, the synthesis of pyrimidine is not that common and is usually performed by removing functional groups from derivatives. Primary syntheses in quantity involving formamide have been reported.[12]:241–242

As a class, pyrimidines are typically synthesized by the principal synthesis involving cyclization of β-dicarbonyl compounds with N–C–N compounds. Reaction of the former with amidines to give 2-substituted pyrimidines, with urea to give 2-pyrimidinones, and guanidines to give 2-aminopyrimidines are typical.[12]:149–239

Pyrimidines can be prepared via the Biginelli reaction. Many other methods rely on condensation of carbonyls with diamines for instance the synthesis of 2-thio-6-methyluracil from thiourea and ethyl acetoacetate[17] or the synthesis of 4-methylpyrimidine with 4,4-dimethoxy-2-butanone and formamide.[18]

A novel method is by reaction of N-vinyl and N-aryl amides with carbonitriles under electrophilic activation of the amide with 2-chloro-pyridine and trifluoromethanesulfonic anhydride:[19]

Reactions

Because of the decreased basicity compared to pyridine, electrophilic substitution of pyrimidine is less facile. Protonation or alkylation typically takes place at only one of the ring nitrogen atoms. Mono-N-oxidation occurs by reaction with peracids.[4]:253–254

Electrophilic C-substitution of pyrimidine occurs at the 5-position, the least electron-deficient. Nitration, nitrosation, azo coupling, halogenation, sulfonation, formylation, hydroxymethylation, and aminomethylation have been observed with substituted pyrimidines.[12]:9–13

Nucleophilic C-substitution should be facilitated at the 2-, 4-, and 6-positions but there are only a few examples. Amination and hydroxylation has been observed for substituted pyrimidines. Reactions with Grignard or alkyllithium reagents yield 4-alkyl- or 4-aryl pyrimidine after aromatization.[12]:14–15

Free radical attack has been observed for pyrimidine and photochemical reactions have been observed for substituted pyrimidines.[12]:15–16 Pyrimidine can be hydrogenated to give tetrahydropyrimidine.[12](pp17)

Nucleotides

The pyrimidine nitrogen bases found in DNA and RNA.

Three nucleobases found in nucleic acids, cytosine (C), thymine (T), and uracil (U), are pyrimidine derivatives:
Cytosine (C)
Thymine (T)
Uracil (U)

In DNA and RNA, these bases form hydrogen bonds with their complementary purines. Thus, in DNA, the purines adenine (A) and guanine (G) pair up with the pyrimidines thymine (T) and cytosine (C), respectively.

In RNA, the complement of adenine (A) is uracil (U) instead of thymine (T), so the pairs that form are adenine:uracil and guanine:cytosine.

Very rarely, thymine can appear in RNA, or uracil in DNA, but when the other three major pyrimidine bases are represented, some minor pyrimidine bases can also occur in nucleic acids. These minor pyrimidines are usually methylated versions of major ones and are postulated to have regulatory functions.[20]

These hydrogen bonding modes are for classical Watson–Crick base pairing. Other hydrogen bonding modes ("wobble pairings") are available in both DNA and RNA, although the additional 2′-hydroxyl group of RNA expands the configurations, through which RNA can form hydrogen bonds.

Theoretical aspects

In March 2015, NASA Ames scientists reported that, for the first time, complex DNA and RNA organic compounds of life, including uracil, cytosine and thymine, have been formed in the laboratory under outer space conditions, using starting chemicals, such as pyrimidine, found in meteorites. Pyrimidine, like polycyclic aromatic hydrocarbons (PAHs), the most carbon-rich chemical found in the universe, may have been formed in red giants or in interstellar dust and gas clouds.[21][22][23]

See also

References

  1. ↑ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 141. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  2. ↑ Brown, H. C.; et al. (1955). Baude, E. A.; F. C., Nachod, eds. Determination of Organic Structures by Physical Methods. New York, NY: Academic Press.
  3. ↑ Gilchrist, Thomas Lonsdale (1997). Heterocyclic chemistry. New York: Longman. ISBN 0-582-27843-0.
  4. 1 2 3 Joule, John A.; Mills, Keith, eds. (2010). Heterocyclic Chemistry (5th ed.). Oxford: Wiley. ISBN 978-1-405-13300-5.
  5. 1 2 Lagoja, Irene M. (2007). "Pyrimidine as Constituent of Natural Biologically Active Compounds" (PDF). Chemistry and Biodiversity. 2 (1): 1–50. doi:10.1002/cbdv.200490173. PMID 17191918.
  6. ↑ Grimaux, E. (1879). "Synthèse des dérivés uriques de la série de l'alloxane" [Synthesis of urea derivatives of the alloxan series]. Comptes rendus hebdomadaires des séances de l'Académie des Sciences. 88: 85–87.
  7. ↑ Kenner, G. W.; Todd, Alexander (1957). Elderfield, R.C., ed. Heterocyclic Compounds. 6. New York: Wiley. p. 235.
  8. ↑ Pinner, A. (1884). "Ueber die Einwirkung von Acetessigäther auf die Amidine" [On the effect of acetylacetonate ester on amidines]. Berichte der Deutschen Chemischen Gesellschaft. A17: 2519–2520.
  9. ↑ Pinner, A. (1885). "Ueber die Einwirkung von Acetessigäther auf die Amidine. Pyrimidin" [On the effect of acetylacetonate ester on amidines. Pyrimidine]. Berichte der Deutschen Chemischen Gesellschaft. A18: 759–760.
  10. ↑ Gabriel, S. (1900). "Pyrimidin aus Barbitursäure" [Pyrimidine from barbituric acid]. Berichte der Deutschen Chemischen Gesellschaft. A33: 3666.
  11. ↑ Lythgoe, B.; Rayner, L. S. (1951). "Substitution Reactions of Pyrimidine and its 2- and 4-Phenyl Derivatives". Journal of the Chemical Society. 1951: 2323–2329. doi:10.1039/JR9510002323.
  12. 1 2 3 4 5 6 7 8 9 Brown, D. J.; Evans, R. F.; Cowden, W. B.; Fenn, M. D. (1994). The Pyrimidines. New York, NY: John Wiley & Sons. ISBN 0-471-50656-7.
  13. 1 2 Albert, Adrien (1968). Heterocyclic Chemistry, an Introduction. London: Athlone Press.
  14. ↑ Kogon, Irving C.; Minin, Ronald; Overberger, C. G. "2-Chloropyrimidine". Org. Synth. 35: 34. doi:10.15227/orgsyn.035.0034.; Coll. Vol., 4, p. 182
  15. ↑ Overberger, C. G.; Kogon, Irving C.; Minin, Ronald. "2-(Dimethylamino)pyrimidine". Org. Synth. 35: 58. doi:10.15227/orgsyn.035.0058.; Coll. Vol., 4, p. 336
  16. ↑ Nuevo, M.; Milam, S. N.; Sandford, S. A.; Elsila, J. E.; Dworkin, J. P. (2009). "Formation of uracil from the ultraviolet photo-irradiation of pyrimidine in pure H2O ices". Astrobiology. 9 (7): 683–695. Bibcode:2009AsBio...9..683N. doi:10.1089/ast.2008.0324. PMID 19778279.
  17. ↑ Foster, H. M.; Snyder, H. R. "4-Methyl-6-hydroxypyrimidine". Org. Synth. 35: 80. doi:10.15227/orgsyn.035.0080.; Coll. Vol., 4, p. 638
  18. ↑ Bredereck, H. "4-methylpyrimidine". Org. Synth. 43: 77. doi:10.15227/orgsyn.043.0077.; Coll. Vol., 5, p. 794
  19. ↑ Movassaghi, Mohammad; Hill, Matthew D. (2006). "Single-Step Synthesis of Pyrimidine Derivatives". J. Am. Chem. Soc. 128 (44): 14254–14255. doi:10.1021/ja066405m.
  20. ↑ Nelson, David L.; Cox, Michael M. (2008). Principles of Biochemistry (5th ed.). W. H. Freeman. pp. 272–274. ISBN 1429208929.
  21. ↑ Marlaire, Ruth (3 March 2015). "NASA Ames reproduces the building blocks of life in laboratory" (Press release). NASA. Retrieved 5 March 2015.
  22. ↑ Nuevo, M.; Chen, Y. J.; Hu, W. J.; Qiu, J. M.; Wu, S. R.; Fung, H. S.; Yih, T. S.; Ip, W. H.; Wu, C. Y. R. (2014). "Photo-irradiation of pyrimidine in pure H2O ice with high-energy ultraviolet photons" (PDF). Astrobiology. 14: 119. doi:10.1089/ast.2013.1093.
  23. ↑ Sandford, S. A.; Bera, P. P.; Lee, T. J.; Materese, C. K.; Nuevo, M. (6 February 2014). "Photosynthesis and photo-stability of nucleic acids in prebiotic extraterrestrial environments" (PDF). Topics of Current Chemistry: 123–164. doi:10.1007/128_2013_499., also published as Barbatti, M.; Borin, A. C.; Ullrich, S. (eds.). "14: Photosynthesis and photo-stability of nucleic acids in prebiotic extraterrestrial environments". Photoinduced phenomena in nucleic acids. Berlin, Heidelberg: Springer-Verlag. p. 499.
This article is issued from Wikipedia - version of the 9/12/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.