866538-99-0

Upstream product

• 120737-59-9 3-methyl-piperazine-1-carboxylic acid tert-butyl ester 
• 369-34-6 3,4-difluoronitrobenzene 
• 866538-95-6 4-(2-fluoro-4-nitro-phenyl)-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 

Downstream Products

• 866539-02-8 4-(4-benzyloxycarbonylamino-2-fluoro-phenyl)-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 
• 866539-17-5 4-{4-[5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenyl}-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 
• 866539-08-4 4-[2-fluoro-4-(5-methanesulfonyloxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 
• 866539-14-2 4-[4-(5-aminomethyl-2-oxo-oxazolidin-3-yl)-2-fluoro-phenyl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 
• 866539-11-9 4-[4-(5-azidomethyl-2-oxo-oxazolidin-3-yl)-2-fluoro-phenyl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 
• 866539-05-1 4-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

N-(3,4-disubstituted phenyl) salicylamide derivatives

A compound represented by the following formula (I) or a salt thereof: wherein R1, R2, R3 and R4 represent hydrogen atom, a halogen atom, cyano group, nitro group, a C1-4 alkyl group, a halogenated C

Synthesis and SAR of novel oxazolidinones: Discovery of ranbezolid

Novel oxazolidinones were synthesized containing a number of substituted five-membered heterocycles attached to the 'piperazinyl-phenyl-oxazolidinone' core of eperezolid. Further, the piperazine ring of the core was replaced by other diamino-heterocycles.