Safety of Phenyl(pyridin-2-yl)methanone. Musci, P; von Keutz, T; Belaj, F; Degennaro, L; Cantillo, D; Kappe, CO; Luisi, R in [Musci, Pantaleo; Degennaro, Leonardo; Luisi, Renzo] Univ Bari A Moro, Flow Chem & Microreactor Technol FLAME Lab, Dept Pharm Drug Sci, Via E Orabona 4, I-70125 Bari, Italy; [von Keutz, Timo; Belaj, Ferdinand; Cantillo, David; Kappe, C. Oliver] Karl Franzens Univ Graz, Inst Chem, Heinrichstr 28, A-8010 Graz, Austria; [von Keutz, Timo; Cantillo, David; Kappe, C. Oliver] Res Ctr Pharmaceut Engn GmbH RCPE, Ctr Continuous Flow Synth & Proc CC FLOW, Inffeldgasse 13, A-8010 Graz, Austria published Flow Technology for Telescoped Generation, Lithiation and Electrophilic (C-3) Functionalization of Highly Strained 1-Azabicyclo[1.1.0]butanes in 2021.0, Cited 32.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.
Strained compounds are privileged moieties in modern synthesis. In this context, 1-azabicyclo[1.1.0]butanes are appealing structural motifs that can be employed as click reagents or precursors to azetidines. We herein report the first telescoped continuous flow protocol for the generation, lithiation, and electrophilic trapping of 1-azabicyclo[1.1.0]butanes. The flow method allows for exquisite control of the reaction parameters, and the process operates at higher temperatures and safer conditions with respect to batch mode. The efficiency of this intramolecular cyclization/C3-lithiation/electrophilic quenching flow sequence is documented with more than 20 examples.
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem