62541-79-1

Upstream product

• 937-18-8 methyl 4-cyanopyrrole-2-carboxylate 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 65561-23-1 N-(E)-Styryl-4-cyano-2-(chlorocarbonyl)pyrrole 
• 65561-21-9 N-(E)-Styryl-4-cyanopyrrole-2-carboxylic Acid 
• 65561-22-0 N-(Z)-Styryl-4-cyanopyrrole-2-carboxylic Acid 
• 86289-04-5 4-Cyano-1-((Z)-styryl)-1H-pyrrole-2-carbonyl chloride 
• 86289-17-0 Sodium N-(2-Hydroxyphenethyl)-4-cyanopyrrole-2-carboxylate 
• 65561-24-2 N-(1,2-Dichlorophenethyl)-4-cyano-2-(chlorocarbonyl)pyrrole 
• 62541-80-4 4-cyano-N-(2-chloro-2-phenylethyl)-pyrrole-2-carbonyl chloride 
• 86289-16-9 Sodium N-Phenacyl-4-cyanopyrrole-2-carboxylate 
• 86289-18-1 Methyl N-(2-Hydroxyphenethyl)-4-cyanopyrrole-2-carboxylate 
• 65561-26-4 7-Cyano-3,4-dihydro-1-oxo-3-phenyl-1H-pyrrolo<1,2-c>morpholine 

Relevant academic research and scientific papers

Pyrrolo[2,1-b] [3]benzazepines useful for producing a skeletal muscle relaxing or tranquilizing effect

11-Aminopropylidene-Pyrrolo[2,1-b] [3]benzazepines are disclosed to have pharmaceutical utility as skeletal muscle relaxants and tranquilizers. They are prepared by a Grignard reaction on pyrrolo[2,1-b] [3]benzazapin-11-ones followed by dehydration, or by a Wittig reaction on the same ketones.

Pyrrolo[2,1-b][3]benzazepines

11H-Pyrrolo[2,1-b][3]benzazepin-11-one and derivatives thereof are generally prepared by Friedel-Crafts ring closure of a N-styrylpyrrole-2-carboxylic acid derivative. They are useful intermediates in the synthesis of skeletal muscle relaxants and tranqui