1393330-83-0

Basic information

• Product Name: (±)-N-(4-fluorophenyl)-2-isopropyl-6-(piperidin-2-yl)imidazo[1,2-a]pyridin-3-amine hydrochloride
• CAS NO: 1393330-83-0
• Molecular Weight: 388.916
• Mol File: 1393330-83-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (±)-N-(4-fluorophenyl)-2-isopropyl-6-(piperidin-2-yl)imidazo[1,2-a]pyridin-3-amine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (±)-N-(4-fluorophenyl)-2-isopropyl-6-(piperidin-2-yl)imidazo[1,2-a]pyridin-3-amine hydrochloride(1393330-83-0)
• EPA Substance Registry System: (±)-N-(4-fluorophenyl)-2-isopropyl-6-(piperidin-2-yl)imidazo[1,2-a]pyridin-3-amine hydrochloride(1393330-83-0)

Safety Data

• Hazardous Substances Data: 1393330-83-0(Hazardous Substances Data)

Upstream product

• 1352522-20-3 (±)-tert-butyl 2-(6-aminopyridin-3-yl)piperidine-1-carboxylate 
• 100133-12-8 (±)-5-(piperidin-2-yl)pyridin-2-amine 
• 53912-89-3 (2S)-2-(3-pyridyl)piperidine hydrochloride 

Relevant articles and documents

Natural products as templates for bioactive compound libraries. 3*. novel heterocycles and peptidomimetics generated from anabasine by isocyanide-based multicomponent reactions

Anabasine served as a starting material for the synthesis of two series of novel, drug-like compounds. On the one hand, anabasine was subjected to a direct Chichibabin amination and elaborated into medicinally relevant, racemic 6-(piperidin-2-yl)imidazo[1,2-a]pyridines via the Groebke-Blackburn reaction. On the other hand, anabasine was used as an amine for the Ugi reaction to provide novel non-racemic anabasine-containing 2-[(2-pyridin-3-yl)piperidin-1-yl] acetamide peptidomimetics with high diastereoselectivity.