145474-81-3

Upstream product

• 145474-68-6 <1-benzyl-2-<(4-fluorobenzoyl)aminomethyl>-5-piperidinyl>methyl 4-fluorobenzoate 
• 145474-68-6 <1-benzyl-2-<(4-fluorobenzoyl)aminomethyl>-5-piperidinyl>methyl 4-fluorobenzoate 
• 145474-70-0 N-<(1-benzyl-5-hydroxymethyl-2-piperidinyl)methyl>-4-fluorobenzamide 
• 145474-70-0 N-<(1-benzyl-5-hydroxymethyl-2-piperidinyl)methyl>-4-fluorobenzamide 
• 145474-79-9 N-(1-Benzyl-5-formyl-piperidin-2-ylmethyl)-4-fluoro-benzamide 
• 132462-28-3 ethyl 1-benzyl-6-cyano-3-piperidinecarboxylate 
• 145474-80-2 N-<<1-benzyl-5-<(N-phenyl)aminomethyl>-2-piperidinyl>methyl>-4-fluorobenzamide 
• 75-36-5 acetyl chloride 
• 145474-80-2 N-<<1-benzyl-5-<(N-phenyl)aminomethyl>-2-piperidinyl>methyl>-4-fluorobenzamide 

Relevant academic research and scientific papers

Mimicking of Ergot Alkaloids and Synthetic Piperidine Drugs by 2,5-Substituted Piperidines Derived from Cis and Trans Ethyl 1-Benzyl-6-Cyano-3-Piperidinecarboxylate.

This report describes the synthesis of pharmacologically interesting 2,5-substituted piperidines from cis and trans ethyl 1-benzyl-6-cyano-3-piperidinecarboxylate 4.Reduction and p-fluorobenzoylation of 4 led to the primary alcohols 7.The alcohols were tr