N-[3-(N-tert-Butoxycarbonylaminooxy)propyl]-2-[2-(3-butynylcarbonylamino)ethylthio]-1,3-benzothiazole-6-carboxamide
We report the synthesis of a modified benzothiazole sulfide. This compound contains a heterocyclic core, a Boc-protected hydroxylamine, and an appended alkyne. This benzothiazole was accessed through three total steps, including an amidation reaction and two nucleophilic aromatic substitutions. The identity of the title compound was confirmed through 1H, 13C, 1H–1H COSY, HSQC, and HMBC NMR, in addition to IR, MALDI-MS, HRMS, and HPLC.
Authors
- Christopher R. Shugrue (ORCID: https://orcid.org/0000-0002-3504-9475)
- Nora N. Veigas
- Gabriella G. Meisner
Institutions
- University of Richmond (US)
Publication Details
- Journal
- Molbank
- Published
- 2026-09-01
- DOI
- https://doi.org/10.3390/m2226
- Primary Topic
- Synthesis and biological activity
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- American Chemical Society Petroleum Research Fund