Rhodium-catalyzed migrative annulation and olefination of 2-aroylpyrroles with diazoesters

• Published in: Organic chemistry frontiers an international journal of organic chemistry 2023-01, Vol.10 (2), p.506-513
• Main Authors: Strashkov, Daniil M, Zavyalov, Kirill V, Sakharov, Pavel A, Agafonova, Anastasiya V, Rostovskii, Nikolai V, Khlebnikov, Alexander F, Novikov, Mikhail S
• Format: Article
• Language: English
• Subjects: Acetic acid; Catalysis; Chemical reactions; Organic chemistry; Pyrroles; Reaction mechanisms; Rhodium; Substitutes
• ISSN: 2052-4110; 2052-4110
• DOI: 10.1039/d2qo01759h

A one-pot synthesis of pyrrolo[1,2-c][1,3]oxazin-1-ones has been developed using the Rh2(OAc)4-catalyzed annulation reaction of 2-aroyl-substituted NH-pyrroles with diazoesters. The reaction, in addition to the annulation product, affords two by-products: pyrrolylpyruvate ester and α-(methoxycarbonyloxy)-β-pyrrol-2-yl cinnamate ester, which are converted to the pyrrolooxazinone derivative under DBU catalysis in a one-pot fashion. Dimethyl diazomalonate reacts with pyrroles containing an acceptor-substituted aroyl group predominantly in the olefination fashion to form the cinnamate derivative, which can be isolated in moderate yields. Olefination of 2-aroylpyrroles is the main reaction when using methyl 2-diazoacetoacetate, methyl 2-diazo-2-(dimethoxyphosphoryl)acetate, and methyl 2-diazo-2-tosylacetate. The diazoester is embedded into both the annulation and olefination products in an unusually rearranged form. The experimental and DFT studies revealed an unprecedented reaction mechanism involving four catalytic cycles, one of which involves catalysis by Rh2(OAc)4, two by the starting pyrrole, and one by the methyl-hemiacetal of the final pyrrolooxazinone.