Pyrrolo[2,1‐ f ][1,2,4]triazin‐4‐amine: Synthesis, C 7‐Functionalization, and NH 2 ‐Derivatization via Buchwald–Hartwig‐Type Coupling
Year: 2025
Type: article
Abstract: An optimized gram‐scale synthetic route to pyrrolo[2,1‐ f ][1,2,4]triazin‐4‐amine is reported, affording an overall yield of 85%. Furthermore, regioselective C 7‐functionalization is achieved via both organometallic and direct strategies, whereas NH 2 ‐derivatization proceeds through Buchwald–Hartwig‐type coupling, providing derivatives in isolated yields ranging from 8% to >99%. These advancements enhance synthetic accessibility and facilitate efficient structural diversification of this significant N ‐heterocycle.
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,330
Awards: G1499616537, G2989526193, G3690646728, G3837754718, G3896905694, G4742337282, Exploring the medicinal chemical space of aromatics with highly selective synthetic tools, NOVAS METODOLOGIAS SINTÉTICAS PARA AS REAÇÕES CATALÍTICAS E ASSIMÉTRICAS DE PASSERINI E UGI: UMA ABORDAGEM EXPERIMENTAL E COMPUTACIONAL
OpenAlex ID: W4415535590
