74205-54-2

Upstream product

• 117721-69-4 2-butoxybenzyl chloride 
• 143-33-9 sodium cyanide 

Downstream Products

• 74316-82-8 1-(2-Butoxy-phenyl)-cyclopentanecarbonitrile 
• 74205-14-4 1-(2-Butoxy-phenyl)-cyclobutanecarbonitrile 
• 117721-70-7 2-(2-Butoxy-phenyl)-3-methyl-butyronitrile 
• 117721-73-0 2-(2-Butoxy-phenyl)-2-isopropyl-5-oxo-pentanenitrile 
• 117721-72-9 2-(2-Butoxy-phenyl)-5,5-diethoxy-2-isopropyl-pentanenitrile 
• 61523-89-5 (2S,5R,6R)-6-{[1-(2-Butoxy-phenyl)-cyclopentanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-37-3 (2S,5R,6R)-6-{[1-(2-Butoxy-phenyl)-cyclobutanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-21-5 (2S,5R,6R)-6-{[1-(2-Butoxy-phenyl)-cyclopropanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-50-0 1-(2-Butoxy-phenyl)-cyclopentanecarboxylic acid 
• 74205-42-8 1-(2-Butoxy-phenyl)-cyclobutanecarboxylic acid 
• 74205-28-0 1-(2-Butoxy-phenyl)-cyclopropanecarboxylic acid 
• 74205-00-8 1-(2-Butoxy-phenyl)-cyclopropanecarbonitrile 

Relevant academic research and scientific papers

SOME NEW ANALOGUES OF VERAPAMIL AND MEPAMIL. SYNTHESIS AND BASIC PHARMACOLOGICAL PROPERTIES

Some new analogues of verapamil (Ia) and mepamil (Ib), calcium antagonists of arylkylamine type, were synthesized and screened for cardiovascular activities.The basic structure was modified a) on the phenyl ring, attached to the quaternary carbon, b) on the alkyl group, attached to the quaternary carbon and c) on the alkylamino group, attached in position 3 to the n-propyl fragment.Except of 2-(2-chlorophenyl)-2-isopropyl-5-(N-methylhomoveratrylamino)valeronitrile (VIa), all the synthesized compounds exhibited lower hypotensive activity, than the mother compound, verapamil.