

SYNTHESIS AND ANTIMYCOBACTERIAL ACTIVITY OF PYRIDINIUM COMPOUNDS WITH SULFONYLACETAMIDE SUBSTITUENT IN N-ALKYL CHAIN

Abstract
Pyridines containing amine, amide, or hydrazide substituent were quaternized with (ω-haloalkyl)sulfonylacetamides, resulting in new pyridinium compounds that exhibited tuberculostatic activity against the strain H37Rv of Mycobacterium tuberculosis.
Authors: Marina M. Shulaeva*, Marionella A. Kravchenko, Vyacheslav E. Semenov
Keywords
carbamoylmethylsulfonyl group; pyridinium compounds; sulfonylacetamides; quaternization; antituberculosis activity
Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv