1220596-13-3

Basic information

• Product Name: benzyl 2-(6-(methylamino)pyridin-2-yl)ethylcarbamate
• Synonyms: benzyl 2-(6-(methylamino)pyridin-2-yl)ethylcarbamate
• CAS NO: 1220596-13-3
• Molecular Weight: 285.346
• Mol File: 1220596-13-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: benzyl 2-(6-(methylamino)pyridin-2-yl)ethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-(6-(methylamino)pyridin-2-yl)ethylcarbamate(1220596-13-3)
• EPA Substance Registry System: benzyl 2-(6-(methylamino)pyridin-2-yl)ethylcarbamate(1220596-13-3)

Safety Data

• Hazardous Substances Data: 1220596-13-3(Hazardous Substances Data)

Upstream product

• 84713-20-2 benzyl N-vinylcarbamate 
• 89026-79-9 2-bromo-6-(methylamino)pyridine 

Downstream Products

• 1227094-87-2 1-(3,4-dichlorobenzyl)-3-(2-(6-(methylamino)pyridin-2-yl)ethyl)urea 

Relevant articles and documents

COMPOUNDS USEFUL AS CHEMOKINE RECEPTOR ANTAGONISTS

The present invention relates to a compound having the general Formula I: Formula I wherein the variables are as defined in the specification. The present invention further relates to pharmaceutical compositions comprising these compounds and to their use

Direct synthesis of Cbz-protected (2-amino)-6-(2-aminoethyl)pyridines

A novel series of (2-amino)-6-(2-aminoethyl)pyridines were prepared by a convenient Suzuki-Miyaura coupling approach from 2-amino-6-bromopyridines. Benzyl vinylcarbamate was first treated with 9-BBN followed by aqueous NaOH and then the appropriate bromopyridine precursors were added into the mixture. The mixture was finally heated in presence of a palladium catalyst to provide the corresponding products in overall high yields. The procedure is extended to the preparation of related pyrazine and pyrimidine compounds as well as (2-amido)- and (2-alkoxy)-6-(2-aminoethyl)pyridines.