Synthesis of Sulfachloropyridazine-Benzene Ring-13C6

Abstract

A synthesis route for stable isotope-labeled sulfamethoxazole-benzene ring-13C6 has been developed. In this strategy, 13C6-benzene was used as the source and starting material for stable isotope labeling and starting material to synthesize sulfachloropyridazine-benzene ring-13C6 through 6 steps of nitration, nitroreduction, acylation, sulfonation, condensation and hydrolysis. The product structure was confirmed through characterization techniques such as nuclear magnetic resonance spectroscopy (NMR) and mass spectrometry (MS), which the purity of the product was higher than 98.0% and the isotopic enrichment was higher than 99.0atom%13C. Sulfachloropyridazine-benzene ring-13C6 can be used as an internal standard reagent for qualitative and quantitative analysis of sulfachlorpyridazine.

Keywords

• stable isotope labeling
• sulfachloropyridazine
• synthesis