Thiazole

Summary

Thiazole, or 1,3-thiazole, is a 5-membered heterocyclic compound that contains both sulfur and nitrogen. The term 'thiazole' also refers to a large family of derivatives. Thiazole itself is a pale yellow liquid with a pyridine-like odor and the molecular formula C3H3NS.[2] The thiazole ring is notable as a component of the vitamin thiamine (B1).

Thiazole
Full structural formula
Skeletal formula with numbers
Ball-and-stick model
Space-filling model
Names
Preferred IUPAC name
1,3-Thiazole
Other names
Thiazole
Identifiers
  • 288-47-1 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:43732 checkY
ChEMBL
  • ChEMBL15605 checkY
ChemSpider
  • 8899 checkY
ECHA InfoCard 100.005.475 Edit this at Wikidata
  • 9256
UNII
  • 320RCW8PEF checkY
  • DTXSID2059776 Edit this at Wikidata
  • InChI=1S/C3H3NS/c1-2-5-3-4-1/h1-3H checkY
    Key: FZWLAAWBMGSTSO-UHFFFAOYSA-N checkY
  • InChI=1/C3H3NS/c1-2-5-3-4-1/h1-3H
    Key: FZWLAAWBMGSTSO-UHFFFAOYAI
  • n1ccsc1
Properties
C3H3NS
Molar mass 85.12 g·mol−1
Boiling point 116 to 118 °C (241 to 244 °F; 389 to 391 K)
Acidity (pKa) 2.5 (of conjugate acid) [1]
-50.55·10−6 cm3/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Molecular and electronic structure edit

Thiazoles are members of the azoles, heterocycles that include imidazoles and oxazoles. Thiazole can also be considered a functional group when part of a larger molecule.

Being planar thiazoles are characterized by significant pi-electron delocalization and have some degree of aromaticity, moreso than the corresponding oxazoles. This aromaticity is evidenced by the 1H NMR chemical shift of the ring protons, which absorb between 7.27 and 8.77 ppm, indicating a strong diamagnetic ring current. The calculated pi-electron density marks C5 as the primary site for electrophilic substitution, and C2-H as susceptible to deprotonation.

Occurrence of thiazoles and thiazolium salts edit

 
Bleomycin is a thiazole-containing anti-cancer drug.

Thiazoles are found in a variety of specialized products, often fused with benzene derivatives, the so-called benzothiazoles. In addition to vitamin B1, the thiazole ring is found in epothilone. Other important thiazole derivatives are benzothiazoles, for example, the firefly chemical luciferin. Whereas thiazoles are well represented in biomolecules, oxazoles are not. It is found in naturally occurring peptides, and utilised in the development of peptidomimetics (i.e. molecules that mimic the function and structure of peptides).[3]

Commercial significant thiazoles include mainly dyes and fungicides. Thifluzamide, Tricyclazole, and Thiabendazole are marketed for control of various agricultural pests. Another widely used thiazole derivative is the non-steroidal anti-inflammatory drug Meloxicam. The following anthroquinone dyes contain benzothiazole subunits: Algol Yellow 8 (CAS# [6451-12-3]), Algol Yellow GC (CAS# [129-09-9]), Indanthren Rubine B (CAS# [6371-49-9]), Indanthren Blue CLG (CAS# [6371-50-2], and Indanthren Blue CLB (CAS#[6492-78-0]). These thiazole dye are used for dyeing cotton.

Synthesis edit

Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis, which is a reaction between haloketones and thioamides. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone.[4] In the Cook-Heilbron synthesis, thiazoles arise by the condensation of α-aminonitrile with carbon disulfide. Thiazoles can be accessed by acylation of 2-aminothiolates, often available by the Herz reaction.

Biosynthesis edit

Thiazoles are generally formed via reactions of cysteine, which provides the N-C-C-S backbone of the ring. Thiamine does not fit this pattern however. Several biosynthesis routes lead to the thiazole ring as required for the formation of thiamine.[5] Sulfur of the thiazole is derived from cysteine. In anaerobic bacteria, the CN group is derived from dehydroglycine.

Reactions edit

With a pKa of 2.5 for the conjugate acid, thiazoles are far less basic than imidazole (pKa =7).[6]

Deprotonation with strong bases occurs at C2-H. The negative charge on this position is stabilized as an ylide. Hauser bases and organolithium compounds react at this site, replacing the proton. 2-Lithiothiazoles are also generated by metal-halogen exchange from 2-bromothiazole.[7]

 

Electrophilic aromatic substitution at C5 but require activating groups such as a methyl group, as illustrated in bromination:

 
Thiazole bromination
 
Thiazole Nucleophilic Aromatic Substitution

Oxidation at nitrogen gives the aromatic thiazole N-oxide; many oxidizing agents exist, such as mCPBA; a novel one is hypofluorous acid prepared from fluorine and water in acetonitrile; some of the oxidation takes place at sulfur, leading to non-aromatic sulfoxide/sulfone:[8] Thiazole N-oxides are useful in Palladium-catalysed C-H arylations, where the N-oxide is able to shift the reactivity to reliably favor the 2-position, and allows for these reactions to be carried out under much more mild conditions.[9]

 
Thiazole oxidation
 
Thiazole cycloaddition

Thiazolium salts edit

Alkylation of thiazoles at nitrogen forms a thiazolium cation. Thiazolium salts are catalysts in the Stetter reaction and the Benzoin condensation. Deprotonation of N-alkyl thiazolium salts give the free carbenes[11] and transition metal carbene complexes.

 
Structure of thiazoles (left) and thiazolium salts (right)

Alagebrium is a thiazolium-based drug.

References edit

  1. ^ Zoltewicz, J. A.; Deady, L. W. (1978). "Quaternization of Heteroaromatic Compounds: Quantitative Aspects". Advances in Heterocyclic Chemistry Volume 22. Vol. 22. pp. 71–121. doi:10.1016/S0065-2725(08)60103-8. ISBN 9780120206223.
  2. ^ Eicher, T.; Hauptmann, S. (2003). The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications. Wiley. ISBN 978-3-527-30720-3.
  3. ^ Mak, Jeffrey Y. W.; Xu, Weijun; Fairlie, David P. (2015-01-01). Peptidomimetics I (PDF). Topics in Heterocyclic Chemistry. Vol. 48. Springer Berlin Heidelberg. pp. 235–266. doi:10.1007/7081_2015_176. ISBN 978-3-319-49117-2.
  4. ^ George Schwarz (1945). "2,4-Dimethylthiazole". Organic Syntheses. 25: 35. doi:10.15227/orgsyn.025.0035.
  5. ^ Kriek, M.; Martins, F.; Leonardi, R.; Fairhurst, S. A.; Lowe, D. J.; Roach, P. L. (2007). "Thiazole Synthase from Escherichia coli: An Investigation of the Substrates and Purified Proteins Required for Activity in vitro" (PDF). J. Biol. Chem. 282 (24): 17413–17423. doi:10.1074/jbc.M700782200. PMID 17403671.
  6. ^ Thomas L. Gilchrist (1997). Heterocyclic Chemistry (3 ed.). Essex, England: Addison Wesley. p. 414. ISBN 0-582-27843-0.
  7. ^ a b Dondoni, A.; Merino, P. (1995). "Diastereoselective Homologation of D-(R)-Glyceraldehyde Acetonide using 2-(Trimethylsilyl)thiazole". 72: 21. doi:10.15227/orgsyn.072.0021. {{cite journal}}: Cite journal requires |journal= (help)
  8. ^ Amir, E.; Rozen, S. (2006). "Easy Access to the Family of Thiazole N-oxides using HOF·CH3CN". Chemical Communications. 2006 (21): 2262–2264. doi:10.1039/b602594c. PMID 16718323.
  9. ^ Campeau, Louis-Charles; Bertrand-Laperle, Mégan; Leclerc, Jean-Philippe; Villemure, Elisia; Gorelsky, Serge; Fagnou, Keith (2008-03-01). "C2, C5, and C4 Azole N -Oxide Direct Arylation Including Room-Temperature Reactions". Journal of the American Chemical Society. 130 (11): 3276–3277. doi:10.1021/ja7107068. ISSN 0002-7863. PMID 18302383.
  10. ^ Alajarín, M.; Cabrera, J.; Pastor, A.; Sánchez-Andrada, P.; Bautista, D. (2006). "On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes". J. Org. Chem. 71 (14): 5328–5339. doi:10.1021/jo060664c. PMID 16808523.
  11. ^ Arduengo, A. J.; Goerlich, J. R.; Marshall, W. J. (1997). "A Stable Thiazol-2-ylidene and Its Dimer". Liebigs Annalen. 1997 (2): 365–374. doi:10.1002/jlac.199719970213.