Facile Regioselective Synthesis of Pyrrolo-Pyrones: Tandem Reaction of 4- N-(4 -Aryloxy-2 -ynyl), N-Methyl Pyran-2-Ones with 3-Chloroperoxybenzoic Acid (Experimental Section)

Title: Facile Regioselective Synthesis of Pyrrolo-Pyrones: Tandem Reaction of 4- N-(4 -Aryloxy-2 -ynyl), N-Methyl Pyran-2-Ones with 3-Chloroperoxybenzoic Acid (Experimental Section)

Volume: 2 Issue: 8

Author(s): Krishna C. Majumdar, Habibur Rahaman and Brindaban Roy

Affiliation:

Keywords: Amine-oxide rearrangement, [2,3]-sigmatropic rearrangement, pyrrolo-pyrone, heterocycles, N-(4-aryloxybut-2-ynyl)-N-methylamine, m-Chloroperoxybenzoic acid

Abstract: A number of 6-methyl-4-N-(4-aryloxybut-2-ynyl)-N-methylaminopyran-2-ones (3a-g) on treatment with one equivalent of 3-chloroperoxybenzoic acid at 0-5 C during 25 minutes and then stirring at room temperature for 9 h afforded pyrrolo[3,2-c]pyrone derivatives (4a-g) in (80-85 %) yield. 6-Methyl-4-N-(4- aryloxybut-2-ynyl)N-methylaminopyran-2-ones (3a-g) were in turn prepared from 4-tosyloxy-6-methylpyran- 2-ones (1) and N-(4-aryloxybut-2-ynyl)- N-methylamine (2a-g).

Cite this article as:

Majumdar C. Krishna, Rahaman Habibur and Roy Brindaban, Facile Regioselective Synthesis of Pyrrolo-Pyrones: Tandem Reaction of 4- N-(4 -Aryloxy-2 -ynyl), N-Methyl Pyran-2-Ones with 3-Chloroperoxybenzoic Acid (Experimental Section), Letters in Organic Chemistry 2005; 2 (8) . https://dx.doi.org/10.2174/157017805774717580