315701-24-7

Upstream product

• 315701-23-6 4-{1-[4-(4-methoxy-phenylsulfanyl)-phenyl]-vinyl}-piperidine-1-carboxylic acid tert-butyl ester 
• 696-63-9 4-Methoxybenzenethiol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 25519-78-2 4-(4-fluorobenzoyl)piperidine hydrochloride 
• 160296-40-2 tert-butyl 1-[4-(4-fluorobenzoyl)piperidin-1-yl]carboxylate 
• 182141-56-6 4-[4-(4-methoxy-phenylsulfanyl)-benzoyl]-piperidine-1-carboxylic acid tert-butyl ester 

Downstream Products

• 182144-07-6 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester 
• 182144-25-8 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl 
• 315701-25-8 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-piperidine 

Relevant academic research and scientific papers

Design and synthesis of piperidinyl piperidine analogues as potent and selective M2 muscarinic receptor antagonists

Identification of a number of highly potent M2 receptor antagonists with >100-fold selectivity against the M1 and M3 receptor subtypes is described. In the rat microdialysis assay, this series of compounds showed pronounced enhancement of brain acetylcholine release after oral administration. (C) 2000 Elsevier Science Ltd.