647858-27-3

Upstream product

• 647858-23-9 [4-(2-benzyloxy-ethoxy)-3-fluoro-phenyl]-carbamic acid benzyl ester 
• 647858-19-3 2-(2-fluoro-4-nitrophenoxy)ethan-1-ol 
• 100-39-0 benzyl bromide 
• 647858-21-7 1-(2-Benzyloxy-ethoxy)-2-fluoro-4-nitro-benzene 

Downstream Products

• 647858-55-7 Methanesulfonic acid 2-{4-[(S)-5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-ethyl ester 
• 647858-29-5 N-{3-[3-fluoro-4-(2-hydroxy-ethoxy)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide 

Relevant academic research and scientific papers

Influence of ethylene-oxy spacer group on the activity of linezolid: Synthesis of potent antibacterials possessing a thiocarbonyl group

The influence of an ethylene-oxy spacer element between the heterocycle and the aromatic ring in linezolid is reported. The introduction of such spacer group generated compounds with inferior antibacterial activity. However, the conversion of the acetamide group present in the linezolid analogues to either thiocarbamate or thioacetamide functionality restored the activity. The synthesis of linezolid analogues possessing the ethylene-oxy spacer group along with SAR studies with different heterocycles and preparation of some thiocarbonyl compounds possessing potent antibacterial property are presented.