Imidazole
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| Names |
| IUPAC name
1H-Imidazole
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Other names
1,3-diazole
glyoxaline (archaic)
1,3-diazacyclopenta-2,4-diene |
| Identifiers |
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CAS Registry Number
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288-32-4 Y |
| ChEBI |
CHEBI:16069 Y |
| ChEMBL |
ChEMBL540 Y |
| ChemSpider |
773 Y |
| EC number |
206-019-2 |
InChI
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InChI=1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5) Y
Key: RAXXELZNTBOGNW-UHFFFAOYSA-N Y
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InChI=1/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)
Key: RAXXELZNTBOGNW-UHFFFAOYAS
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| Jmol-3D images |
Image |
| KEGG |
C01589 Y |
| PubChem |
795 |
| RTECS number |
NI3325000 |
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| Properties |
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Chemical formula
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C3H4N2 |
| Molar mass |
68.077 g/mol |
| Appearance |
white or pale yellow solid |
| Density |
1.23 g/cm3, solid |
| Melting point |
89 to 91 °C (192 to 196 °F; 362 to 364 K) |
| Boiling point |
256 °C (493 °F; 529 K) |
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Solubility in water
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Soluble |
| Acidity (pKa) |
14.5 (for imidazole) and 7.05 (for the conjugate acid) [1] |
| UV-vis (λmax) |
280 nm |
| Structure |
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Crystal structure
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monoclinic |
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Coordination geometry
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planar 5-membered ring |
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Dipole moment
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3.61D |
| Hazards |
| Main hazards |
Corrosive |
| Safety data sheet |
External MSDS |
| R-phrases |
R20 R22 R34 R41 |
| S-phrases |
S26 S36 S37 S39 S45 |
| Flash point |
146 °C (295 °F; 419 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Y verify (what is: Y/N?) |
| Infobox references |
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Imidazole is an organic compound with the formula (CH)2N(NH)CH. It is a colourless solid that dissolves in water to give mildly alkaline solution. In chemistry, it is an aromatic heterocycle, classified as a diazole. It is a white or colorless solid that is soluble in water.
Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles, share the 1,3-C3N2 ring but feature varied substituents. This ring system is present in important biological building-blocks, such as histidine, and the related hormone histamine. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.[2][3][4][5][6]
When fused to a pyrimidine ring, it forms purine, which is the most widely occurring nitrogen-containing heterocycle in nature.[7]
Contents
- 1 Structure and properties
- 2 Preparation
- 3 Biological significance and applications
- 3.1 Pharmaceutical derivatives
- 4 Industrial applications
- 5 Salts of imidazole
- 6 Related heterocycles
- 7 See also
- 8 References
Structure and properties
Imidazole is a planar 5-membered ring. It exists in two equivalent tautomeric forms, because the proton can be located on either of the two nitrogen atoms. Imidazole is a highly polar compound, as evidenced by a calculated dipole of 3.61D. It is highly soluble in water. The compound is classified as aromatic due to the presence of a sextet of π-electrons, consisting of a pair of electrons from the protonated nitrogen atom and one from each of the remaining four atoms of the ring. Some resonance structures of imidazole are shown below:
Amphoterism
Imidazole is amphoteric. That is, it can function as both an acid and as a base. As an acid, the pKa of imidazole is 14.5, making it less acidic than carboxylic acids, phenols, and imides, but slightly more acidic than alcohols. The acidic proton is located on N-1. As a base, the pKa of the conjugate acid (cited above as pKBH+ to avoid confusion between the two) is approximately 7, making imidazole approximately sixty times more basic than pyridine. The basic site is N-3. Protonation gives the imidazolium cation, which is symmetrical.
Preparation
Imidazole was first reported in 1858, although various imidazole derivatives had been discovered as early as the 1840s. Its synthesis, as shown below, used glyoxal and formaldehyde in ammonia to form imidazole (or glyoxaline, as it was originally named).[8] This synthesis, while producing relatively low yields, is still used for creating C-substituted imidazoles.
In one microwave modification, the reactants are benzil, benzaldehyde and ammonia in glacial acetic acid, forming 2,4,5-triphenylimidazole (Lophine).[9]
Imidazole can be synthesized by numerous methods besides the Debus method. Many of these syntheses can also be applied to different substituted imidazoles and imidazole derivatives by varying the functional groups on the reactants. These methods are commonly categorized by which and how many bonds form to make the imidazole rings. For example, the Debus method forms the (1,2), (3,4), and (1,5) bonds in imidazole, using each reactant as a fragment of the ring, and thus this method would be a three-bond-forming synthesis. A small sampling of these methods is presented below.
- Formation of one bond
- The (1,5) or (3,4) bond can be formed by the reaction of an imidate and an α-aminoaldehyde or α-aminoacetal, resulting in the cyclization of an amidine to imidazole. The example below applies to imidazole when R=R1=Hydrogen.
- Formation of two bonds
- The (1,2) and (2,3) bonds can be formed by treating a 1,2-diaminoalkane, at high temperatures, with an alcohol, aldehyde, or carboxylic acid. A dehydrogenating catalyst, such as platinum on alumina, is required.
- The (1,2) and (3,4) bonds can also be formed from N-substituted α-aminoketones and formamide with heat. The product will be a 1,4-disubstituted imidazole, but here since R=R1=Hydrogen, imidazole itself is the product. The yield of this reaction is moderate, but it seems to be the most effective method of making the 1,4 substitution.
- Formation of four bonds
- This is a general method that is able to give good yields for substituted imidazoles. In essence, it is an adaptation of the Debus method called the Debus-Radziszewski imidazole synthesis. The starting materials are substituted glyoxal, aldehyde, amine, and ammonia or an ammonium salt.[10]
- Formation from other heterocycles
- Imidazole can be synthesized by the photolysis of 1-vinyltetrazole. This reaction will give substantial yields only if the 1-vinyltetrazole is made efficiently from an organotin compound, such as 2-tributylstannyltetrazole. The reaction, shown below, produces imidazole when R=R1=R2=Hydrogen.
- Imidazole can also be formed in a vapor-phase reaction. The reaction occurs with formamide, ethylenediamine, and hydrogen over platinum on alumina, and it must take place between 340 and 480 °C. This forms a very pure imidazole product.
- Van Leusen reaction
- The Van Leusen reaction can also be employed to form imidazoles starting from TosMIC and an aldimine.
Biological significance and applications
Imidazole is incorporated into many important biological molecules. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes and plays a vital part in the structure and binding functions of hemoglobin. Imidazole-based histidine compounds play a very important role in intracellular buffering.[11] Histidine can be decarboxylated to histamine, which is also a common biological compound. It can cause urticaria (hives), when histamine is produced during allergic reaction. The relationship between histidine and histamine are shown below:
One of the applications of imidazole is in the purification of His-tagged proteins in immobilised metal affinity chromatography (IMAC). Imidazole is used to elute tagged proteins bound to Ni ions attached to the surface of beads in the chromatography column. An excess of imidazole is passed through the column, which displaces the His-tag from nickel co-ordination, freeing the His-tagged proteins.
Imidazole has become an important part of many pharmaceuticals. Synthetic imidazoles are present in many fungicides and antifungal, antiprotozoal, and antihypertensive medications. Imidazole is part of the theophylline molecule, found in tea leaves and coffee beans, that stimulates the central nervous system. It is present in the anticancer medication mercaptopurine, which combats leukemia by interfering with DNA activities.
A number of substituted imidazoles, including clotrimazole, are selective inhibitors of nitric oxide synthase, which makes them interesting drug targets in inflammation, neurodegenerative diseases and tumors of the nervous system.[12][13] Other biological activities of the imidazole pharmacophore relate to the downregulation of intracellular Ca++ and K+ fluxes, and interference with translation initiation.[14]
Pharmaceutical derivatives
The substituted imidazole derivatives are valuable in treatment of many systemic fungal infections.[15] Imidazoles belong to the class of azole antifungals, which includes ketoconazole, miconazole, and clotrimazole.
For comparison, another group of azoles is the triazoles, which includes fluconazole, itraconazole, and voriconazole. The difference between the imidazoles and the triazoles involves the mechanism of inhibition of the cytochrome P450 enzyme. The N3 of the imidazole compound binds to the heme iron atom of ferric cytochrome P450, whereas the N4 of the triazoles bind to the heme group. The triazoles have been shown to have a higher specificity for the cytochrome P450 than imidazoles, thereby making them more potent than the imidazoles.[16]
Some imidazole derivatives show effects on insects, for example sulconazole nitrate exhibits a strong anti-feeding effect on the keratin-digesting Australian carpet beetle larvae Anthrenocerus australis, as does econazole nitrate with the common clothes moth Tineola bisselliella.[17]
Industrial applications
Imidazole has been used extensively as a corrosion inhibitor on certain transition metals, such as copper. Preventing copper corrosion is important, especially in aqueous systems, where the conductivity of the copper decreases due to corrosion.
Many compounds of industrial and technological importance contain imidazole derivatives. The thermostable polybenzimidazole PBI contains imidazole fused to a benzene ring and linked to a benzene, and acts as a fire retardant. Imidazole can also be found in various compounds that are used for photography and electronics.
Salts of imidazole
Salts of imidazole where the imidazole ring is in the cation are known as imidazolium salts (for example, imidazolium chloride). These salts are formed from the protonation or substitution at nitrogen of imidazole. These salts have been used as ionic liquids and precursors to stable carbenes. Salts where a deprotonated imidazole is an anion are also well known; these salts are known as imidazolates (for example, sodium imidazolate, NaC3H3N2).
Related heterocycles
- Benzimidazole, an analog with a fused benzene ring
- Dihydroimidazole or imidazoline, an analog where 4,5-double bond is saturated
- Pyrrole, an analog with only one nitrogen atom in position 1
- Oxazole, an analog with the nitrogen atom in position 1 replaced by oxygen
- Thiazole, an analog with the nitrogen atom in position 1 replaced by sulfur
- Pyrazole, an analog with two adjacent nitrogen atoms
- Triazoles, analogs with three nitrogen atoms
See also
- 1-Methylimidazole
- 4-Methylimidazole
References
- ^ Walba, H. & Isensee, R. W. Acidity constants of some arylimidazoles and their cations. J. Org. Chem. 26, 2789-2791 (1961). doi:10.1021/jo01066a039
- ^ Alan R. Katritzky; Rees. Comprehensive Heterocyclic Chemistry. Vol. 5, p.469-498, (1984).
- ^ Grimmett, M. Ross. Imidazole and Benzimidazole Synthesis. Academic Press, (1997).
- ^ Brown, E.G. Ring Nitrogen and Key Biomolecules. Kluwer Academic Press, (1998).
- ^ Pozharskii, A.F, et al. Heterocycles in Life and Society. John Wiley & Sons, (1997).
- ^ Heterocyclic Chemistry TL Gilchrist, The Bath press 1985 ISBN 0-582-01421-2
- ^ Rosemeyer, H (2004). Chemistry & Biodiversity 1: 361. doi:10.1002/cbdv.200490033.
- ^ Heinrich Debus (1858). "Ueber die Einwirkung des Ammoniaks auf Glyoxal". Annalen der Chemie und Pharmacie 107 (2): 199–208. doi:10.1002/jlac.18581070209.
- ^ Microwave-Mediated Synthesis of Lophine: Developing a Mechanism To Explain a Product Crouch, R. David; Howard, Jessica L.; Zile, Jennifer L.; Barker, Kathryn H. J. Chem. Educ. 2006 83 1658
- ^ US patent 6,177,575, A. J. Arduengo, "Process for Manufacture of Imidazoles", issued 2001-01-23
- ^ Hochachka, P.W. & G.N. Somero, 2002. Biochemical adaptation: mechanisms and process in physiological evolution. New York: Oxford University Press. 466 p.
- ^ Castaño T, Encinas A, Pérez C, Castro A, Campillo NE, Gil C. (2008). "Design, synthesis, and evaluation of potential inhibitors of nitric oxide synthase."Bioorg Med Chem. 16 (11) : 6193-206. PMID 18477512
- ^ Bogle RG, Whitley GS, Soo SC, Johnstone AP, Vallance P. (1994). "Effect of anti-fungal imidazoles on mRNA levels and enzyme activity of inducible nitric oxide synthase". Br J Pharmacol. 111 (4) : 1257-61. PMC1910171
- ^ Khalid MH, Tokunaga Y, Caputy AJ, Walters E. (2005)."Inhibition of tumor growth and prolonged survival of rats with intracranial gliomas following administration of clotrimazole." J Neurosurg. 103 (1) : 79-86. PMID 16121977
- ^ Leon Shargel. Comprehensive Pharmacy Review (6th ed.). p. 930.
- ^ Riviere and Papich. Veterinary Pharmacology and Therapeutics (9th ed.). pp. 1019–1020.
- ^ Sunderland, M. R.; Cruickshank, R. H.; Leighs, S. J. (2014). “The efficacy of antifungal azole and antiprotozoal compounds in protection of wool from keratin-digesting insect larvae”. Textile Research Journal 84 (9): 924–931. http://trj.sagepub.com/content/84/9/924
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Antifungals (D01 and J02)
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Wall/
membrane |
Ergosterol
inhibitors |
Azoles
(lanosterol 14
alpha-demethylase inhibitors) |
| Imidazoles |
- Topical: bifonazole
- butoconazole
- chlormidazole
- clotrimazole#
- croconazole
- econazole
- fenticonazole
- ketoconazole
- isoconazole
- miconazole#
- neticonazole
- omoconazole
- oxiconazole
- sertaconazole
- sulconazole
- tioconazole
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| Triazoles |
- Topical: (fluconazole#, fosfluconazole
- terconazole)
- Systemic: (fluconazole
- hexaconazole
- isavuconazole
- itraconazole
- posaconazole
- voriconazole)
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| Thiazoles |
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Polyene antimycotics
(ergosterol binding) |
- Topical: (hamycin
- natamycin
- nystatin#)
Systemic: (amphotericin B#, hamycin)
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Allylamines
(squalene monooxygenase
inhibitors) |
- Topical: (amorolfine
- butenafine
- naftifine
- terbinafine)
Systemic: terbinafine
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β-glucan synthase
inhibitors |
- echinocandins (anidulafungin
- caspofungin
- micafungin)
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| Intracellular |
Pyrimidine analogues/
thymidylate synthase inhibitors |
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| Mitotic inhibitors |
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| Aminoacyl tRNA synthetase inhibitors |
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| Others |
- bromochlorosalicylanilide
- methylrosaniline
- tribromometacresol
- undecylenic acid
- polynoxylin
- chlorophetanol
- chlorphenesin
- ticlatone
- sulbentine
- ethylparaben
- haloprogin
- salicylic acid
- selenium disulfide#
- ciclopirox
- amorolfine
- dimazole
- tolnaftate
- tolciclate
- sodium thiosulfate#
- Whitfield's ointment#
- potassium iodide#
- taurolidine
- tea tree oil
- citronella oil
- lemon grass
- orange oil
- patchouli
- lemon myrtle
- PCP: pentamidine
- dapsone
- atovaquone
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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Index of fungal disease
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| Description |
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| Disease |
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| Treatment |
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| Authority control |
- GND: 4161307-7
- NDL: 00564035
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