65095-75-2

Usage

InChI:InChI=1/C9H12N2O3S2/c1-3-14-6(13)4-5(12)7-8(10)11-9(15-2)16-7/h3-4,10H2,1-2H3

Upstream product

• 638-07-3 ethyl (2-chloroaceto)acetate 
• 10191-61-4 potassium methyl cyanoiminodithiocarbonate 
• 36239-09-5 ethyl chlorocarbonylacetate 
• 10191-61-4 potassium S-methyl N-cyanocarbamodithioate 
• 13176-46-0 4-bromoethyl acetoacetate 

Downstream Products

• 94507-68-3 4-Ethyl-4,7-dihydro-2-(4-phenylpiperazinyl)-7-oxothiazolo<4,5-b>pyridine-6-carboxylic Acid 
• 94507-69-4 4-Ethyl-4,7-dihydro-2-(4-benzylpiperazinyl)-7-oxothiazolo<4,5-b>pyridine-6-carboxylic Acid 
• 94507-59-2 4-Ethyl-4,7-dihydro-2-<(4-hydroxy-4-phenyl)piperidino>-7-oxothiazolo<4,5-b>pyridine-6-carboxylic Acid 
• 94507-70-7 4-Ethyl-4,7-dihydro-2-<4-(4-chlorobenzhydryl)piperazinyl>-7-oxothiazolo<4,5-b>pyridine-6-carboxylic Acid 

Relevant academic research and scientific papers

Antibacterial compounds

Bacterial protein synthesis-inhibiting compounds having formula (I) and salts, prodrugs, and salts of prodrugs thereof, processes for making the compounds and intermediates in the processes, compositions containing the compounds, and methods of using the compounds are disclosed.

FACILE SYNTHESIS OF THIAZOLO- AND THIENOPYRIDINE DERIVATIVES BY A NOVEL PYRIDINE CYCLIZATION REACTION VIA ENAMINE INTERMEDIATES

Thiazolo- and thienopyridine-6-carboxylic acid derivatives were synthesized by formation of the thiazole or the thiophene ring bearing o-amino-β-ketoester moiety, followed by a novel pyridine cyclization reaction with DMF-dimethylacetal.