69634-21-5

Basic information

• Product Name: N-(3-aminopyridin-2-yl)benzamide
• Synonyms: N-(3-aminopyridin-2-yl)benzamide
• CAS NO: 69634-21-5
• Molecular Weight: 213.239
• Mol File: 69634-21-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(3-aminopyridin-2-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-aminopyridin-2-yl)benzamide(69634-21-5)
• EPA Substance Registry System: N-(3-aminopyridin-2-yl)benzamide(69634-21-5)

Safety Data

• Hazardous Substances Data: 69634-21-5(Hazardous Substances Data)

Upstream product

• 452-58-4 2,3-Diaminopyridine 
• 100-52-7 benzaldehyde 
• 878398-49-3 N-(3-nitropyridin-2-yl)benzamide 
• 99314-92-8 N²-amino-N³-benzyloxycarbonylaminopyridine 
• 99314-94-0 (2-Benzoylamino-pyridin-3-yl)-carbamic acid benzyl ester 

Downstream Products

• 1016-93-9 2-phenyl-1H-imidazo<4,5-b>pyridine 
• 32282-07-8 N²-benzyl-2,3-pyridinediamine 

Relevant articles and documents

Microwave-assisted heteropolyanion-based ionic liquid promoted sustainable protocol to N-heteroaryl amides via N-directing dual catalyzed oxidative amidation of aldehydes

A sustainable procedure for the synthesis of N-heteroaryl amides directly from oxidative amidation of aldehydes catalyzed by heteropolyanion-based ionic liquids under microwave-promoted conditions has been reported. The transformation has proven to tolerate a wide range of aldehydes and amino heterocycles with different functional groups. Moderate to excellent yields, solvent-free media, operational simplicity and reusability of catalysts are the main highlights. Furthermore, the proposed N-directing dual-catalysis mechanistic pathway was briefly investigated in this report.

A new route to N2- and N3-substituted-2,3-diaminopyridines. Synthesis of 1- and 3-alkoxycarbonyl-v-triazolo[4,5-b]pyridines

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