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Synthesis of 4-[4-(3-pyridinyl)imidazol-1-yl]-1-butylamine.

Authors :
Cao, Zhiling
Liu, Bing
Liu, Weiwei
Yao, Guowei
Li, Hongxia
Zou, Ting
Source :
Journal of Chemical Research; 2011, Vol. 35 Issue 10, p600-601, 2p, 1 Diagram
Publication Year :
2011

Abstract

4-[4-(3-pyridinyl)imidazol-1-yl]-1-butylamine, the side chain of telithromycin, is used for the synthesis of novel ketolide antibiotics. The key step in synthesising 4-[4-(3-pyridinyl)imidazol-1-yl]-1-butylamine involves the HBr-induced DMSO oxidation of 3-acetylpyridine to 3-pyridylglyoxal, which was not isolated but transformed directly into 4-(3-pyridyl)imidazole by a Debus reaction with ammonia and formaldehyde. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17475198
Volume :
35
Issue :
10
Database :
Complementary Index
Journal :
Journal of Chemical Research
Publication Type :
Academic Journal
Accession number :
74021180
Full Text :
https://doi.org/10.3184/174751911X13176543106368