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Synthesis of 7-Aminocoumarins from 7-Hydroxycoumarins via Amide Smiles Rearrangement.
Lippe, Daniel S; Elghawy, Omar; Zucker, Adam M; Yanagawa, Evan S K; Mathews, Erin; Ahmed, Yusef G; D'Elia, Paige N; Bimson, Sabrina; Walvoord, Ryan R.
Afiliação
  • Lippe DS; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Elghawy O; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Zucker AM; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Yanagawa ESK; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Mathews E; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Ahmed YG; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • D'Elia PN; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Bimson S; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
  • Walvoord RR; Department of Chemistry, Ursinus College, Collegeville, Pennsylvania 19426, United States.
ACS Omega ; 7(39): 35269-35279, 2022 Oct 04.
Article em En | MEDLINE | ID: mdl-36211046
ABSTRACT
N-Substituted 7-aminocoumarins can be synthesized from readily available 7-hydroxycoumarins via alkylation with α-bromoacetamides and subsequent tandem O → N Smiles rearrangement-amide hydrolysis. The key rearrangement sequence proceeds under mild conditions to provide convenient access to various N-alkyl and N-aryl products in moderate to high yields. The process is operationally simple, inexpensive, transition-metal-free, and can be telescoped into a one-pot process.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article