1370229-89-2

Upstream product

• 1370229-55-2 C₁₁H₁₄ClNO₅S 
• 263854-45-1 N-(3,5-dimethoxyphenyl)methanesulfonamide 
• 10272-07-8 3.5-dimethoxyaniline 
• 108-24-7 acetic anhydride 
• 1370229-79-0 (6,8-dimethoxy-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-5-ylmethyl)carbamic acid tert-butyl ester 
• 1370229-72-3 dithiocarbonic acid S-{1-((tert-butoxycarbonylamino)methyl)-4-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-4-oxo-butyl} ester O-ethyl ester 
• 1370229-62-1 dithiocarbonic acid S-{2-[methanesulfonyl(3,5-dimethoxyphenyl)amino]-2-oxo-ethyl} ester O-ethyl ester 

Relevant academic research and scientific papers

Desulfonylative radical ring closure onto aromatics. A modular route to benzazepin-2-ones and 5-arylpiperidin-2-ones

Adducts from the intermolecular radical addition of N-xanthylacetyl-N- methanesulfanilides to Boc-protected allylamine undergo ring closure with loss of a methanesulfonyl radical to give benzazepin-2-ones. Upon deprotection and exposure to triethylamine,