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Benzimidazole is a . This bicyclic compound may be viewed as fused rings of the aromatic compounds and . It is a white solid that appears in form of tabular crystals.


Preparation
Benzimidazole was discovered during research on vitamin B12. The benzimidazole nucleus was found to be a stable platform on which drugs could be developed. Benzimidazole is produced by condensation of o-phenylenediamine with , or the equivalent trimethyl orthoformate:
C6H4(NH2)2 + HC(OCH3)3 → C6H4N(NH)CH + 3 CH3OH

2-Substituted derivatives are obtained when the condensation is conducted with in place of formic acid, followed by .


Reactions
Benzimidazole is a base:
C6H4N(NH)CH + H+ → C6H4(NH)2CH+
It can also be with stronger bases:
C6H4N(NH)CH + LiH → Li C6H4N2CH + H2

The can be and also serves as a ligand in coordination chemistry. The most prominent benzimidazole complex features N-ribosyl-dimethylbenzimidazole, as found in vitamin B12.

N, N'-Dialkylbenzimidazolium salts are precursors to certain N-heterocyclic carbenes.


Applications
Benzimidazole derivatives are among the most frequently used ring systems for drugs listed by the United States Food and Drug Administration.Taylor, R. D.; MacCoss, M.; Lawson, A. D. G. J Med Chem 2014, 57, 5845.> Many pharmaceutical agents belong to the benzimidazole class of compounds. For example:

In printed circuit board manufacturing, benzimidazole can be used as an organic solderability preservative.

Several are derived from benzimidazoles.


See also


Further reading

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