147740-01-0

Usage

Uses

Used in Pharmaceutical Synthesis:
Ethyl5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals for its unique structural attributes that can be leveraged to create novel drug molecules.
Used in Organic Chemistry:
In the field of organic chemistry, Ethyl5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate serves as a building block, facilitating the creation of complex organic compounds and contributing to the advancement of chemical research and development.
Used in Research and Development:
Ethyl5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate is utilized in research and development settings to explore its potential applications and to understand its properties further. Its unique structure may lead to the discovery of new uses in various industries.

InChI:InChI=1/C10H12N2O2/c1-2-14-10(13)12-6-8-4-3-5-11-9(8)7-12/h3-5H,2,6-7H2,1H3

Downstream Products

• 344459-54-7 N-[[(5S)-3-[4-(5,7-dihydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide 
• 344460-45-3 methanesulfonic acid 3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester 
• 344460-43-1 [4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-carbamic acid benzyl ester 
• 344460-47-5 5-aminomethyl-3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-oxazolidin-2-one 
• 344459-52-5 (5R)-3-[4-(5,7-Dihydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-3-fluorophenyl]-5-(hydroxymethyl)-2-oxazolidinone 
• 344460-40-8 6,7-Dihydro-6-(2-fluoro-4-nitrophenyl)-5H-pyrrolo[3,4-b]pyridine 
• 344460-41-9 6,7-Dihydro-6-(2-fluoro-4-aminophenyl)-5H-pyrrolo[3,4-b]pyridine 
• 344459-88-7 C₁₈H₁₈FN₇O₄ 
• 906480-73-7 acetic acid ({3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamoyl)-methyl ester 
• 344459-84-3 C₂₀H₁₉FN₆O₂S 
• 906480-78-2 6-{3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethoxy}-nicotinonitrile 
• 344459-70-7 cyclopropanecarboxylic acid {3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-amide 
• 906480-77-1 3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-5-(6-methyl-pyridin-2-yloxymethyl)-oxazolidin-2-one 
• 344459-68-3 N-{3-[4-(5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-propionamide 

Relevant academic research and scientific papers

Antibacterial activity of pyrrolopyridine-substituted oxazolidinones: synthesis and in vitro SAR of various C-5 acetamide replacements

A series of pyrrolopyridine-substituted oxazolidinones containing various C-5 acetamide isosteres was synthesized and the structure-antibacterial activity relationships determined against a representative panel of susceptible and resistant Gram-positive b

7-azaisoindolinyl-quinolone-carboxylic acid derivatives

The invention relates to new quinolonecarboxylic acid derivatives which are substituted in the 7-position by an optionally partially hydrogenated azaisoindolinyl ring, to processes for their preparation, and to antibacterial agents and feed additives containing them.