194729-09-4

Upstream product

• 6006-82-2 3,4-methylenedioxyphenethyl alcohol 
• 2861-28-1 1,3-benzodioxole-5-acetic acid 

Downstream Products

• 194729-10-7 7,8-methylenedioxy-1-(4-nitrophenyl)-3,5-dihydro-2,3-benzodiazepin-4(4H)-one 
• 862457-87-2 (2,2-dimethoxy-ethyl)-[5-(4-nitro-phenyl)-7,9-dihydro-1,3-dioxa-6,7-diaza-cyclohepta[f]inden-8-ylidene]-amine 
• 862457-90-7 8,9-dibromo-5-(4-nitrophenyl)-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2,3]benzodiazepine 
• 862457-91-8 C₁₈H₁₂Br₂N₄O₂ 
• 194729-28-7 5-(4-Nitrophenyl)-11H-1,3-dioxolo[4,5-h]imidazo[1,2-c][2.3]benzodiazepine 
• 194729-29-8 C₁₈H₁₄N₄O₂ 
• 194729-11-8 5-(4-nitrophenyl)-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-8(9H)-thione 
• 862457-88-3 C₁₈H₁₃N₃O₂ 

Relevant academic research and scientific papers

Novel α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptor antagonists of 2,3-benzodiazepine type: Chemical synthesis, in vitro characterization, and in vivo prevention of acute neurodegeneration

Under pathophysiological conditions, α-amino-3-hydroxy-5-methyl-4- isoxazole propionate (AMPA) receptor activation is considered to play a key role in several disorders of the central nervous system. In the search for AMPA receptor antagonists, the synthe

Method for the production of imidazo-(1,2-C)(2,3)-benzodiazepines and intermediates in the production thereof

The invention relates to a method for the preparation of compound of formula (1). The invention further relates to the previously unknown compounds of formulas (5 and 6) as intermediates in the production of benzodiazepines of formula (1).