Methyl (1aRS,7aSR)-7-formyl-1a-phenyl-1,1a-dihydroazirino[2,3-b]benzo[e][1,4]thiazine-7a(7H)-carboxylate
The first representative of the aziridine-fused benzo[e][1,4]thiazine series was synthesized from methyl 2-bromo-2-phenyl-2H-azirine-2-carboxylate and benzo[d]thiazole in 74% yield. The reaction proceeds via the SN2′-SN2′-cascade to form the azirinylthiazolium salt followed by a water-induced thiazole ring expansion. The structure of the title compound was established based on 1H, 13C, 2D NMR spectroscopy and high-resolution mass spectrometry, and unambiguously confirmed by X-ray diffraction analysis.
Authors
- Николай В. Ростовский (ORCID: https://orcid.org/0000-0002-8925-794X)
- Anastasiya V. Agafonova (ORCID: https://orcid.org/0000-0003-1855-7440)
- Ilya P. Filippov (ORCID: https://orcid.org/0000-0001-8869-2539)
- Михаил С. Новиков (ORCID: https://orcid.org/0000-0001-5106-4723)
Institutions
- St Petersburg University (RU)
Publication Details
- Journal
- Molbank
- Published
- 2025-12-04
- DOI
- https://doi.org/10.3390/m2101
- Primary Topic
- Synthesis and Catalytic Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Russian Science Foundation