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.

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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

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article

N-[3-(N-tert-Butoxycarbonylaminooxy)propyl]-2-[2-(3-butynylcarbonylamino)ethylthio]-1,3-benzothiazole-6-carboxamide

Christopher R. Shugrue, Nora N. Veigas, Gabriella G. Meisner
Molbank
Synthesis and biological activity
article

N-[3-(N-tert-Butoxycarbonylaminooxy)propyl]-2-[2-(3-butynylcarbonylamino)ethylthio]-1,3-benzothiazole-6-carboxamide

Christopher R. Shugrue, Nora N. Veigas, Gabriella G. Meisner
article en

Abstract

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.

MolbankVol. 2026(5)
University of Richmond (US)
American Chemical Society Petroleum Research Fund
Clean water and sanitation
Openalex Percentile: Top 20%
Synthesis and biological activity
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