1395322-86-7

Basic information

• Product Name: 2-(2-fluoro-4-nitrophenyl)-5-oxohexahydrocyclopenta[c]pyrrole
• Synonyms: 2-(2-fluoro-4-nitrophenyl)-5-oxohexahydrocyclopenta[c]pyrrole
• CAS NO: 1395322-86-7
• Molecular Weight: 264.256
• Mol File: 1395322-86-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(2-fluoro-4-nitrophenyl)-5-oxohexahydrocyclopenta[c]pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-fluoro-4-nitrophenyl)-5-oxohexahydrocyclopenta[c]pyrrole(1395322-86-7)
• EPA Substance Registry System: 2-(2-fluoro-4-nitrophenyl)-5-oxohexahydrocyclopenta[c]pyrrole(1395322-86-7)

Safety Data

• Hazardous Substances Data: 1395322-86-7(Hazardous Substances Data)

Upstream product

• 1395322-85-6 2-(2-fluoro-4-nitrophenyl)-octahydro-5-hydroxycyclopenta[c]pyrrole 
• 1417820-59-7 octahydro-5-hydroxycyclopenta[c]pyrrole hydrochloride 
• 203663-25-6 t-butyl 5-hydroxy-3,3a,4,5,6,6a-hexahydro-1H-cyclopenteno[c]pyrrole-2-carboxylate 

Downstream Products

• 1395322-88-9 2-(4-amino-2-fluorophenyl)-hexahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane] 
• 1395322-90-3 (5R)-3-(3-fluoro-4-(tetrahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane]-2(3H)-yl)phenyl)-5-(hydroxymethyl)oxazolidin-2-one 
• 1417820-60-0 2-[2-fluoro-4-[(5R)-5-[[(methylsulfonyl)oxy]methyl]-2-oxo-3-oxazolidinyl]phenyl]-hexahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane] 
• 1395322-91-4 (5R)-5-(azidomethyl)-3-(3-fluoro-4-(tetrahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane]-2(3H)-yl)phenyl)-oxazolidin-2-one 
• 1395322-92-5 N-(((5S)-3-(3-fluoro-4-(tetrahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane]-2(3H)-yl)phenyl)-2-oxo-oxazolidin-5-yl)methyl)acetamide 
• 1395322-93-6 (5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(tetrahydro-1H-spiro[cyclopenta[c]pyrrole-5,2'-[1,3]dioxolane]-2(3H)-yl)phenyl)oxazolidin-2-one 
• 1395322-94-7 N-(((5S)-3-(3-fluoro-4-(5-oxohexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)-2-oxo-oxazolidin-5-yl)methyl)acetamide 
• 1395322-97-0 (5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(hydroxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one 
• 1395322-98-1 N-(((5S)-3-(3-fluoro-4-(5-(methoxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)-2-oxo-oxazolidin-5-yl)methyl)acetamide 
• 1395322-99-2 (5R)-5-((1H-1,2,3-triazol-1-yl)methyl)-3-(3-fluoro-4-(5-(methoxyimino)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)phenyl)oxazolidin-2-one 
• 1395323-00-8 N-(((5S)-3-(4-(5-(cyanomethylene)hexahydrocyclopenta[c]pyrrol-2(1H)-yl)-3-fluorophenyl)-2-oxo-oxazolidin-5-yl)methyl)acetamide 
• 1395323-01-9 2-(2-(4-((R)-5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxo-oxazolidin-3-yl)-2-fluorophenyl)hexahydrocyclopenta[c]pyrrol-5(1H)-ylidene)acetonitrile 
• 1395323-02-0 N-[[(5S)-3-[4-(5-cyanomethyl-3,3a,4,6a-tetrahydro-1H-cyclopenta[c]pyrrol-2-yl)-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide 
• 1395323-03-1 2-(2-(4-((R)-5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxo-oxazolidin-3-yl)-2-fluorophenyl)-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrol-5-yl)acetonitrile 

Relevant articles and documents

Synthesis and In Vitro Antibacterial Activity of Novel 3-Azabicyclo[3.3.0]octanyl Oxazolidinones

We synthesized a series of oxazolidinone-type antibacterials in which morpholine C-ring of linezolid has been modified by substituted 3-azabicyclo[3.3.0]octanyl rings. Acetamide or 1,2,3-triazole heterocycle was used as C-5 side chain of oxazolidinone. The resulting series of compounds was then screened in vitro against panel of susceptible and resistant Gram-positive, Gram-negative bacteria, and Mycobacterium tuberculosis (Mtb). Several analogs in this series exhibited potent in vitro antibacterial activity comparable or superior to linezolid against the tested bacteria. Compounds 10a, 10b, 11a, and 15a displayed highly potent activity against M. tuberculosis. Selected compound 10b showed good human microsomal stability and CYP-profile, and showed low activity against hERG channel. We synthesized a series of oxazolidinone-type antibacterials in which morpholine C-ring of linezolid has been modified by substituted 3-azabicyclo[3.3.0]octanyl rings, and acetamide or 1,2,3-triazole heterocycle was used as C-5 side chain of oxazolidinone. Several analogs in this series exhibited potent in vitro antibacterial activity comparable or superior to linezolid against panel of susceptible and resistant Gram-positive, Gram-negative bacteria and Mycobacterium tuberculosis (Mtb). Compounds 10a, 10b, 11a, and 15a displayed highly potent activity against M. tuberculosis.