Thiazole

Thiazole, or 1,3-thiazole, is a clear to pale yellow flammable liquid with a pyridine-like odor and the molecular formula C₃H₃NS. It is a 5-membered ring, in which two of the vertices of the ring are nitrogen and sulfur, and the other three are carbons ^[1].

Thiazole is used for manufacturing biocides, fungicides, pharmaceuticals, and dyes.

Additional recommended knowledge

Essential Laboratory Skills Guide

How to quickly check pipettes?

Safe Weighing Range Ensures Accurate Results

Thiazoles and thiazolium salts

Thiazoles are a class of organic compounds related to azoles with a common thiazole functional group. Thiazoles are aromatic.

The thiazole moiety is a crucial part of vitamin B1 (thiamine) and epothilone. Other important thiazoles are benzothiazoles, for example, the firefly chemical luciferin.

Thiazoles are structurally similar to imidazoles. Like imidazoles, thiazoles have been used to give N-S free carbenes^[2] and transition metal carbene complexes.^{[citation needed]}

When the amino atom is alkylated, the resulting thiazolium salt is a salt. Thiazolium salts are catalysts in the Stetter reaction and the Benzoin condensation. Thiazole dyes are used for dying cotton.

Oxazoles are related compounds, with sulfur replaced by oxygen. Thiazoles are well represented in biomolecules; oxazoles are not.

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 though application of the Herz reaction.

Reactions

Thiazoles are characterized by larger pi-electron delocalization than the corresponding oxazoles and have therefore greater aromaticity. This is evidenced by the position of the ring protons in proton NMR (between 7.27 and 8.77 ppm), clearly indicating a strong diamagnetic ring current.

The calculated pi-electron density marks C5 as the primary electrophilic site, and C2 as the nucleophilic site.

The reactivity of a thiazole can be summarized as follows:

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

2-(trimethylsiliyl)thiazole ^[5] (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

• Alkylation at nitrogen forms a thiazolium salt
• 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 a sulfoxide ^[6]:

• Thiazoles are formyl synthons; conversion of R-thia to the R-CHO aldehyde takes place with ^[5], respectively, methyl iodide (N-methylation), organic reduction with sodium borohydride, and hydrolysis with mercury 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.

References

1. ^ The Chemistry of Heterocycles : Structure, Reactions, Syntheses, and Applications Theophil Eicher, Siegfried Hauptmann ISBN 3-527-30720-6
2. ^ A. J. Arduengo, J. R. Goerlich and W. J. Marshall (1997). "A Stable Thiazol-2-ylidene and Its Dimer". Liebigs Annalen 1997 (2): 365-374. doi:10.1002/jlac.199719970213.
3. ^ George Schwarz (1955). "2,4-Dimethylthiazole". Org. Synth.; Coll. Vol. 3: 332. 
4. ^ ^{a b} Mateo Alajarín, José Cabrera, Aurelia Pastor, Pilar Sánchez-Andrada, and Delia Bautista (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.
5. ^ ^{a b} Alessandro Dondoni and Pedro Merino (1998). "Diastereoselective Homologation of D-(R)-Glyceraldehyde Acetonide using 2-(Trimethylsilyl)thiazole". Org. Synth.; Coll. Vol. 9: 952. 
6. ^ Elizabeta Amir and Shlomo Rozen (2006). "Easy access to the family of thiazole N-oxides using HOF·CH3CN". Chemical Communications 2006: 2262 - 2264. doi:10.1039/b602594c.