A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). Heterocyclic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of these heterocycles.
Examples of heterocyclic compounds include all of the nucleic acids, the majority of drugs, most biomass (cellulose and related materials), and many natural and synthetic dyes. 59% of US FDA-approved drugs contain nitrogen heterocycles.
- 1 Classification
- 2 3-membered rings
- 3 4-membered rings
- 4 5-membered rings
- 5 6-membered rings
- 6 7-membered rings
- 7 8-membered rings
- 8 9-membered rings
- 9 Images
- 10 Fused rings
- 11 History of heterocyclic chemistry
- 12 Uses
- 13 References
- 14 External links
Although heterocyclic chemical compounds may be inorganic compounds or organic compounds, most contain at least one carbon. While atoms that are neither carbon nor hydrogen are normally referred to in organic chemistry as heteroatoms, this is usually in comparison to the all-carbon backbone. But this does not prevent a compound such as borazine (which has no carbon atoms) from being labelled "heterocyclic". IUPAC recommends the Hantzsch-Widman nomenclature for naming heterocyclic compounds.
Heterocyclic compounds can be usefully classified based on their electronic structure. The saturated heterocycles behave like the acyclic derivatives. Thus, piperidine and tetrahydrofuran are conventional amines and ethers, with modified steric profiles. Therefore, the study of heterocyclic chemistry focuses especially on unsaturated derivatives, and the preponderance of work and applications involves unstrained 5- and 6-membered rings. Included are pyridine, thiophene, pyrrole, and furan. Another large class of heterocycles are fused to benzene rings, which for pyridine, thiophene, pyrrole, and furan are quinoline, benzothiophene, indole, and benzofuran, respectively. Fusion of two benzene rings gives rise to a third large family of compounds, respectively the acridine, dibenzothiophene, carbazole, and dibenzofuran. The unsaturated rings can be classified according to the participation of the heteroatom in the conjugated system, pi system.
Heterocycles with three atoms in the ring are higher in energy and more reactive because of ring strain. Those containing one heteroatom are, in general, stable. Those with two heteroatoms are more likely to occur as reactive intermediates. The C-X-C bond angles (where X is a heteroatom) in oxiranes and aziridines are very close to 60° and the peripheral H-C-H bond angles are near to 180°.
Three-membered rings with one heteroatomEdit
|Oxygen||Oxirane (ethylene oxide, epoxides)||Oxirene|
Three-membered rings with two heteroatomsEdit
Four-membered rings with one heteroatomEdit
Four-membered rings with two heteroatomsEdit
Five-membered rings with one heteroatomEdit
|Nitrogen||Pyrrolidine ("Azolidine" is not used)||Pyrrole ("Azole" is not used)|
Five-membered rings with two heteroatomsEdit
The 5-membered ring compounds containing two heteroatoms, at least one of which is nitrogen, are collectively called the azoles. Thiazoles and isothiazoles contain a sulfur and a nitrogen atom in the ring. Dithiolanes have two sulfur atoms.
|Heteroatom||Saturated||Unsaturated (and partially unsaturated)|
Five-membered rings with at least three heteroatomsEdit
A large group of 5-membered ring compounds with three or more heteroatoms also exists. One example is the class of dithiazoles, which contain two sulfur atoms and one nitrogen atoms.
|3 × Nitrogen||Triazoles|
|2 × Nitrogen / 1 × oxygen||Furazan|
|2 × Nitrogen / 1 × sulfur||Thiadiazole|
|1 × Nitrogen / 2 × oxygen||Dioxazole|
|1 × Nitrogen / 2 × sulfur||Dithiazole|
|4 × Nitrogen||Tetrazole|
|4 × Nitrogen/1 × Oxygen||Oxatetrazole|
|4 × Nitrogen/1 × Sulfur||Thiatetrazole|
|5 × Nitrogen||Pentazole|
Six-membered rings with one heteroatomEdit
|Nitrogen||Piperidine (Azinane is not used)||Pyridine (Azine is not used)||Pyridinium cation|
|Oxygen||Tetrahydropyran||Pyran (2H-Oxine is not used)||Pyrylium cation|
|Sulfur||Thiane||Thiopyran (2H-Thiine is not used)||Thiopyrylium cation|
Six-membered rings with two heteroatomsEdit
|Nitrogen / nitrogen||Piperazine||Diazine|
|Oxygen / nitrogen||Morpholine||Oxazine|
|Sulfur / nitrogen||Thiomorpholine||Thiazine|
|Oxygen / oxygen||Dioxane||Dioxine|
|Sulfur / sulfur||Dithiane||Dithiin|
Six-membered rings with three heteroatomsEdit
Six-membered rings with four heteroatomsEdit
Six-membered rings with five heteroatomsEdit
Six-membered rings with six heteroatomsEdit
The hypothetical compound with six nitrogen heteroatoms would be hexazine.
Borazine is a six-membered ring with three nitrogen heteroatoms and three boron heteroatom.
With 7-membered rings, the heteroatom must be able to provide an empty pi orbital (e.g., boron) for "normal" aromatic stabilization to be available; otherwise, homoaromaticity may be possible. Compounds with one heteroatom include:
Those with two heteroatoms include:
Heterocyclic rings systems that are formally derived by fusion with other rings, either carbocyclic or heterocyclic, have a variety of common and systematic names. For example, with the benzo-fused unsaturated nitrogen heterocycles, pyrrole provides indole or isoindole depending on the orientation. The pyridine analog is quinoline or isoquinoline. For azepine, benzazepine is the preferred name. Likewise, the compounds with two benzene rings fused to the central heterocycle are carbazole, acridine, and dibenzoazepine. Thienothiophene are the fusion of two thiophene rings. Phosphaphenalenes are a tricyclic phosphorus-containing heterocyclic system derived from the carbocycle phenalene.
History of heterocyclic chemistryEdit
The history of heterocyclic chemistry began in the 1800s, in step with the development of organic chemistry. Some noteworthy developments:
1818: Brugnatelli isolates alloxan from uric acid
1832: Dobereiner produces furfural (a furan) by treating starch with sulfuric acid
1834: Runge obtains pyrrole ("fiery oil") by dry distillation of bones
1906: Friedlander synthesizes indigo dye, allowing synthetic chemistry to displace a large agricultural industry
1936: Treibs isolates chlorophyl derivatives from crude oil, explaining the biological origin of petroleum.
1951: Chargaff's rules are described, highlighting the role of heterocyclic compounds (purines and pyrimidines) in the genetic code.
- IUPAC Gold Book heterocyclic compounds
- Thomas L. Gilchrist "Heterocyclic Chemistry" 3rd ed. Addison Wesley: Essex, England, 1997. 414 pp. ISBN 0-582-27843-0.
- Edon Vitaku, David T. Smith, Jon T. Njardarson (2014). "Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals". J. Med. Chem. 57: 10257-10274. doi:10.1021/jm501100b.CS1 maint: multiple names: authors list (link)
- "Stibinin". chemspider. Royal Society of Chemistry. Retrieved 11 June 2018.
- "Bismin". ChemSpider. Royal Society of Chemistry. Retrieved 11 June 2018.
- Campaigne, E. (1986). "Adrien Albert and the rationalization of heterocyclic chemistry". Journal of Chemical Education. 63 (10): 860. doi:10.1021/ed063p860.
- "IPEXL.com Multilingual Patent Search, Patent Ranking". www.ipexl.com.
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