Thiazole

Thiazole

Names
IUPAC name 1,3-Thiazole
Identifiers
CAS Number	288-47-1
ChEBI	CHEBI:43732
ChEMBL	ChEMBL15605
ChemSpider	8899
Jmol 3D image	Interactive graph
PubChem	9256
UNII	320RCW8PEF
InChI InChI=1S/C3H3NS/c1-2-5-3-4-1/h1-3H Key: FZWLAAWBMGSTSO-UHFFFAOYSA-N InChI=1/C3H3NS/c1-2-5-3-4-1/h1-3H Key: FZWLAAWBMGSTSO-UHFFFAOYAI
SMILES n1ccsc1
Properties
Chemical formula	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]
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

Thiazole, or 1,3-thiazole, is a 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).

Molecular and electronic structure

Thiazoles are members of the azoles, heterocycles that include imidazoles and oxazoles. Thiazole can also be considered a functional group. Oxazoles are related compounds, with sulfur replaced by oxygen. Thiazoles are structurally similar to imidazoles, with the thiazole sulfur replaced by nitrogen.

Thiazole rings are planar and aromatic. Thiazoles are characterized by larger pi-electron delocalization than the corresponding oxazoles and have therefore greater aromaticity. This aromaticity is evidenced by the chemical shift of the ring protons in proton NMR spectroscopy (between 7.27 and 8.77 ppm), clearly indicating a strong diamagnetic ring current. The calculated pi-electron density marks C5 as the primary site for electrophilic substitution, and C2 as the site for nucleophilic substitution.

Occurrence of thiazoles and thiazolium salts

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 dervatives are benzothiazoles, for example, the firefly chemical luciferin. Whereas thiazoles are well represented in biomolecules, oxazoles are not.

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 dying cotton.

Organic synthesis

Various laboratory methods exist for the organic synthesis of thiazoles.

• The Hantzsch thiazole synthesis (1889) is a reaction between haloketones and thioamides. For example, 2,4-dimethylthiazole is synthesized from acetamide, phosphorus pentasulfide, and chloroacetone.^[3] Another example ^[4] is given below:

• In an adaptation of the Robinson-Gabriel synthesis, a 2-acylamino-ketones reacts with phosphorus pentasulfide.
• In the Cook-Heilbron synthesis, an α-aminonitrile reacts with carbon disulfide.
• Certain thiazoles can be accessed through application of the Herz reaction.

Biosynthesis

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

The reactivity of a thiazole can be summarized as follows:

• Deprotonation at C2: the negative charge on this position is stabilized as an ylide; Hauser bases and organolithium compounds react at this site, replacing the proton

2-(trimethylsiliyl)thiazole ^[6] (with a trimethylsilyl group in the 2-position) is a stable substitute and reacts with a range of electrophiles such as aldehydes, acyl halides, and ketenes

• Electrophilic aromatic substitution at C5 requires activating groups such as a methyl group in this bromination:

• Nucleophilic aromatic substitution often requires an electrofuge at C2, such as chlorine with

• Organic oxidation at nitrogen gives the 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 sulfoxide/sulfone:^[7]

• Thiazoles are formyl synthons; conversion of R-thia to the R-CHO aldehyde takes place with,^[6] respectively, methyl iodide (N-methylation), organic reduction with sodium borohydride, and hydrolysis with Mercury(II) chloride in water.
• Thiazoles can react in cycloadditions, but in general at high temperatures due to favorable aromatic stabilization of the reactant; Diels-Alder reactions with alkynes are followed by extrusion of sulfur, and the endproduct is a pyridine; in one study,^[4] a very mild reaction of a 2-(dimethylamino)thiazole with dimethyl acetylenedicarboxylate (DMAD) to a pyridine was found to proceed through a zwitterionic intermediate in a formal [2+2]cycloaddition to a cyclobutene, then to a 1,3-thiazepine in an 4-electron electrocyclic ring openening and then to a 7-thia-2-azanorcaradiene in an 6-electron electrocyclic ring, closing before extruding the sulfur atom.

Thiazolium salts

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^[8] and transition metal carbene complexes.

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

Alagebrium is a thiazolium-based drug.

References

1. Zoltewicz, J. A.; Deady, L. W. (1978). "Quaternization of Heteroaromatic Compounds. Quantitative Aspects". Advances in Heterocyclic Chemistry. Advances in Heterocyclic Chemistry 22: 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. ISBN 3-527-30720-6.
3. Schwarz, G. (1945). "2,4-Dimethylthiazole". Org. Synth. 25: 35.; Coll. Vol. 3, p. 332
4. 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.
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. Dondoni, A.; Merino, P. (1995). "Diastereoselective Homologation of D-(R)-Glyceraldehyde Acetonide using 2-(Trimethylsilyl)thiazole". Org. Synth. 72: 21.; Coll. Vol. 9, p. 952
7. 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.
8. 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.