78533-14-9

Upstream product

• 78533-13-8 3,4-dimethoxy-N-(2-hydroxy-2-phenylethyl)benzeneacetamide 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 1268628-06-3 3-benzoyl-7,8-dimethoxy-5-phenyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one 
• 1268628-05-2 3-acetyl-7,8-dimethoxy-5-phenyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one 
• 78533-11-6 2-(3,4-dimethoxyphenyl)-N-(2-oxo-2-phenylethyl)acetamide 
• 10313-60-7 3,4-dimethoxyphenylacetyl chloride 

Downstream Products

• 78533-19-4 2-ethoxy-7,8-dimethoxy-5-phenyl-4,5-dihydro-1H-3-benzazepine 
• 78533-15-0 7,8-dimethoxy-5-phenyl-1,3-dihydro-2H-3-benzazepin-2-one 
• 78533-16-1 2-ethoxy-7,8-dimethoxy-5-phenyl-1H-3-benzazepine 
• 1268628-05-2 3-acetyl-7,8-dimethoxy-5-phenyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one 
• 1268628-06-3 3-benzoyl-7,8-dimethoxy-5-phenyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one 
• 1268628-04-1 3-allyl-7,8-dimethoxy-5-phenyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one 

Relevant academic research and scientific papers

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines: Substrate extension and product utilization

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines was further exploited. Both 1-aryl- and 1-alkyl- or 1-alkenyl-benzazepines underwent this reaction smoothly. The rearrangement products were used to prepare a

The Synthesis of Some 7,8-Dimethoxy-5-phenyl-2H-3-benzazepin-2-one Derivatives

The benzazepin-2-ones 7 and 9 were prepared from homoveratroyl chloride (4) and phenacylamine.Compounds 7 and 9 were used for the preparation of the benzazepin-2-amines 3, 11, 13 and 14.A synthesis of the benzazepine-1,2-dione 17 and the benzazepine-2,4-d