54734-91-7

Upstream product

• 70-11-1 α-bromoacetophenone 
• 3009-97-0 N-phenylglycinonitrile 
• 78366-89-9 [(2-Oxo-2-phenyl-ethyl)-phenyl-amino]-acetonitrile 

Downstream Products

• 54735-05-6 1,10-diphenyl-3,4-dihydro-pyrazino[1,2-a]indole 
• 78367-08-5 1-Methyl-10-phenyl-3,4-dihydro-pyrazino[1,2-a]indole 
• 78367-31-4 N-[2-(3-Phenyl-indol-1-yl)-ethyl]-acetamide 
• 54735-00-1 1-(2-Benzoylaminoaethyl)-3-phenylindol 
• 54734-97-3 2-(3-phenyl-indol-1-yl)-ethylamine 

Relevant academic research and scientific papers

Synthesis of 10-Phenyl-3,4-dihydropyrazinoindoles and 3-Phenylindole-1-acetic Acids

3-Phenylindole-1-acetonitriles (IVa-e) have been prepared by a new method in which appropriate N-phenylglycinonitriles are condensed with phenacyl bromide and then the condensed products are cyclodehydrated with P2O5 in boiling xylene.Catalytic hydrogenat

Preparation of benzodiazepines

A 1-alkyl-1,2,4,5-tetrahydro-3H-1,4-benzodiazepine derivative is produced by contacting a 1-aminoethyl-indole derivative with a suitable oxidizing agent and then reducing the resulting 1-acyl-2,3-dihydro-1H-1,4-benzodiazepine derivative. The starting 1-am