New Route for the Synthesis of Pyrimido[4',5':4,5]thiazolo[3,2-a]benzimidazol-4(3H)-ones
Corresponding Author(s) : A. DAVOODNIA
adavoodnia@yahoo.com; adavoodnia@mshdiau.ac.ir
Asian Journal of Chemistry,
Vol. 22 No. 6 (2010): Vol 22 Issue 6
Abstract
A new route for the synthesis of 2-arylpyrimido[4',5':4,5]thiazolo[3,2- a]benzimidazol-4(3H)ones has been developed through heterocyclization of 3-aminothiazolo[3,2-a]benzimidazol-2-carboxamide with aromatic aldehydes in boiling glacial acetic acid followed by air oxidation.
Keywords
Aromatic aldehydes
Heterocyclization
Pyrimido[4',5':4,5]thiazolo[3,2-a]benzimidazol-4(3H)-ones
3-Aminothiazolo[3,2- a]benzimidazol-2-carboxamide
DAVOODNIA, A., ESHGHI, H., EZZATAHMADI, S., & TAVAKOLI-HOSEINI, N. (2010). New Route for the Synthesis of Pyrimido[4’,5’:4,5]thiazolo[3,2-a]benzimidazol-4(3H)-ones. Asian Journal of Chemistry, 22(6), 4959–4961. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/16839
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