Morita-Baylis-Hillman adducts as building blocks of heterocycles: a simple approach to 4-substituted pyrazolones, and mechanism investigation via ESI-MS(/MS)

Autor(es)

Barcelos, Rosimeire C. ^[1] ; Zeoly, Lucas A. ^[1] ; Rodrigues, Jr., Manoel T. ^[1] ; Ferreira, Bruno R. V. ^[2] ; Eberlin, Marcos N. ^[2] ; Coelho, Fernando ^[1]

Afiliação do(s) autor(es)

^[1] Univ Estadual Campinas, Lab Synth Nat Prod & Drugs, BR-13083970 Campinas, SP - Brazil

^[2] Univ Estadual Campinas, Lab ThoMSon Mass Spectrometry, BR-13083970 Campinas, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: MONATSHEFTE FUR CHEMIE; v. 146, n. 9, p. 1557-1570, SEP 2015.
• Citações Web of Science: 4

Resumo

We describe herein an efficient approach for the preparation of 4-substituted 2,3-dihydro-1H-pyrazol-3-ones starting from Morita-Baylis-Hillman adducts. These heterocycles were obtained in two or three steps as single isomers with moderate to good overall yields. One efficient and alternative methodology for the synthesis of alpha-methyl-beta-ketoesters is also reported (up to 91 % yield). Additionally, the mechanism of formation of pyrazolones was investigated employing ESI-MS/MS reaction monitoring. (AU)

• Processo FAPESP: 12/24783-1 - Morita-Baylis-Hillman em química medicinal: síntese e avaliação biológica neuroprotetora, antimicrobiana e antitumoral de novos heterociclos, oximas e nitronas
• Beneficiário: Rosimeire Coura Barcelos
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado