122081-15-6

Basic information

• Product Name: 4-METHYL-N-(3-OXO-3-(PYRROLIDIN-1-YL)PROPYL)BENZENESULFONAMIDE
• Synonyms: 4-METHYL-N-(3-OXO-3-(PYRROLIDIN-1-YL)PROPYL)BENZENESULFONAMIDE
• CAS NO: 122081-15-6
• Molecular Formula: C₁₄H₂₀N₂O₃S
• Molecular Weight: 296.3852
• Mol File: 122081-15-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-METHYL-N-(3-OXO-3-(PYRROLIDIN-1-YL)PROPYL)BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-N-(3-OXO-3-(PYRROLIDIN-1-YL)PROPYL)BENZENESULFONAMIDE(122081-15-6)
• EPA Substance Registry System: 4-METHYL-N-(3-OXO-3-(PYRROLIDIN-1-YL)PROPYL)BENZENESULFONAMIDE(122081-15-6)

Safety Data

• Hazardous Substances Data: 122081-15-6(Hazardous Substances Data)

Upstream product

• 123-75-1 pyrrolidine 
• 42908-33-8 3-{[(4-methylphenyl)sulfonyl]amino}propanoic acid 
• 98-59-9 p-toluenesulfonyl chloride 
• 61341-03-5 N-(toluene-4-sulfonyl)-β-alanyl chloride 

Downstream Products

• 122080-91-5 3-{[(4-methylphenyl)sulfonyl]-N-(prop-2-en-1-yl)amino}-1-pyrrolidinylpropan-1-one 
• 122080-95-9 N-But-3-enyl-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide 
• 122080-93-7 N-((E)-But-2-enyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide 
• 122080-92-6 4-Methyl-N-(2-methyl-allyl)-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide 
• 122081-00-9 (1R,5S)-1-Methyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.2.0]heptan-6-one 
• 122080-99-3 (cis)-3-[(4-methylphenyl)sulfonyl]-3-azabicyclo[3.2.0]heptan-6-one 
• 122081-06-5 (1S,5R)-3-(Toluene-4-sulfonyl)-3-aza-bicyclo[3.1.1]heptan-6-one 
• 122081-01-0 (1R,5S,7R)-7-Methyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.2.0]heptan-6-one 
• 122081-07-6 (1R,5S,7R)-7-Methyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.1]heptan-6-one 
• 122081-03-2 3-[(4-methylphenyl)sulfonyl]-3-azabicyclo[4.2.0]octan-8-one 
• 122080-99-3 3-[(4-methylphenyl)sulfonyl]-3-azabicyclo[3.2.0]heptan-6-one 

Relevant articles and documents

TRICYCLIC GYRASE INHIBITORS

Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

Intramolecular [2 + 2] cycloadditions of keteniminium salts derived from α- and β-amino acids. A route to azabicyclic ketones

Unsaturated N-tosylaminoketeniminium salts generated in situ from α- and β-aminoamides readily underwent intramolecular [2 + 2]cycloadditions to give azabicyclic ketones in good yields.