Heterocyclic compound

Pyridine, a simple heterocyclic compound

Heterocyclic compounds are organic compounds containing at least one atom of carbon, and at least one element other than carbon, such as sulfur, oxygen or nitrogen within a ring structure.[1] These structures may comprise either simple aromatic rings or non-aromatic rings. Some examples are pyridine (C5H5N), pyrimidine (C4H4N2) and dioxane (C4H8O2).

Note that compounds such as cyclopropane, an anaesthetic with explosive properties, and cyclohexane, a solvent, are not heterocyclic; they are merely cycloalkanes. The stem '-cyclic' implies a ring structure, whereas 'hetero' refers to an atom other than carbon, as above. Many heterocyclic compounds, including some amines, are carcinogenic.

Heterocyclic chemistry is the chemistry branch dealing exclusively with synthesis, properties, and applications of heterocycles. IUPAC name is Hantzsch-Widman nomenclature.

Contents

3-Membered rings

Heterocycles with three atoms in the ring are 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. Common 3-membered heterocycles are:

Heteroatom Saturated Unsaturated
Nitrogen Aziridine Azirine
Oxygen Ethylene oxide (epoxides, oxiranes) Oxirene
Sulfur Thiirane (episulfides)

Those with two heteroatoms include:

Heteroatom Saturated Unsaturated
Oxygen Dioxirane

4-Membered rings

Compounds with one heteroatom:

Heteroatom Saturated Unsaturated
Nitrogen Azetidine
Oxygen Oxetane
Sulfur Thietane

Compounds with two heteroatoms:

Heteroatom Saturated Unsaturated
Oxygen Dioxetane
Sulfur Dithietane Dithiete

5-Membered rings

With heterocycles containing five atoms, the unsaturated compounds are frequently more stable because of aromaticity.

Five-membered rings with a single heteroatom:

Heteroatom Saturated Unsaturated
Nitrogen Tetrahydropyrrole (azolidine, pyrrolidine) Dihydropyrrole (pyrroline), Pyrrole
Oxygen Tetrahydrofuran (oxolane) Dihydrofuran, Furan
Sulfur Tetrahydrothiophene (thiolane) Dihydrothiophene, Thiophene
Arsenic Arsole

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
Nitrogen Imidazolidine Pyrazole, Imidazole
Nitrogen/oxygen Oxazolidine Oxazole, Isoxazole
Nitrogen/sulfur Thiazolidine Thiazole, Isothiazole
Oxygen Dioxolane
Sulfur Dithiolane

A large group of 5-membered ring compounds with three heteroatoms also exists. One example is dithiazoles that contain two sulfur and a nitrogen atom.

Heteroatom Saturated Unsaturated
Nitrogen 1,2,3-Triazole, 1,2,4-Triazole
Nitrogen/2-sulfur Dithiazole

Five-member ring compounds with four heteroatoms:

Heteroatom Saturated Unsaturated
Nitrogen Tetrazole

With 5-heteroatoms, the compound may be considered inorganic rather than heterocyclic. Pentazole is the all nitrogen heteroatom unsaturated compound.

6-Membered rings

Six membered rings with a single heteroatom:

Heteroatom Saturated Unsaturated
Nitrogen Piperidine Pyridine
Oxygen Tetrahydropyran Pyran
Sulfur Thiane Thiine (thiapyrane)

With two heteroatoms:

Heteroatom Saturated Unsaturated
Nitrogen Piperazine Diazines
Nitrogen / oxygen Oxazine
Nitrogen / sulfur Thiazine
Sulfur Dithiane
Oxygen Dioxane Dioxin

With three heteroatoms:

Heteroatom Saturated Unsaturated
Nitrogen Triazine

With four heteroatoms:

Heteroatom Saturated Unsaturated
Nitrogen Tetrazine

The hypothetical compound with six nitrogen heteroatoms would be hexazine.

7-Membered rings

With 7-membered rings, aromatic stabilization is not available. Compounds with one heteroatom include:

Heteroatom Saturated Unsaturated
Nitrogen Azepine
Sulfur Thiepin

Those with two heteroatoms include:

Heteroatom Saturated Unsaturated
Nitrogen Diazepine

Fused rings

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. Similarly, the compounds with two benzene rings fused to the central heterocycle are carbazole, acridine, and dibenzoazepine.

References

  1. Eicher, T.; Hauptmann, S. (2nd ed. 2003). The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications. Wiley-VCH. ISBN 3527307206. 

External links