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ChemicalBook CAS DataBase List 5-Bromo-2-chloro-3-nitropyridine
67443-38-3

5-Bromo-2-chloro-3-nitropyridine synthesis

7synthesis methods
-

Yield:67443-38-3 84%

Reaction Conditions:

with lithium chloride

Steps:

2
The λ/-[5-(5-amino-6-chloropyridin-3-yl)thiazol-2-yl]acetamide used as a starting material was prepared as follows :-Using an analogous procedure to that described by K. Jouve and J. Bergman, J. Heterocyclic Chem., 2003, 40, 261 except that one equivalent of lithium chloride was used, 2-amino-5-bromo-3-nitropyridine was converted in 84% yield into 5-bromo-2-chloro-3-nitropyridine; 1H νMR Spectrum: (CDCl3) 8.37 (IH, d), 8.7 (IH, d); which, in turn, was converted into 3-amino-5-bromo-2-chloropyridine; 1H νMR Spectrum: (CDCl3) 4.17 (2H, br s), 7.18 (IH, d), 7.85 (IH, d).

References:

ASTRAZENECA AB;ASTRAZENECA UK LIMITED WO2007/129044, 2007, A1 Location in patent:Page/Page column 77

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