Synthetic access to 2-amido-5-aryl-8-methoxy-triazolopyridine and 2-amido-5-morpholino-8-methoxy-triazolopyridine derivatives as potential inhibitors of the adenosine receptor subtypes

Synthesis

Volumn , Issue 11, 2003, Pages 1649-1652

  Nettekoven, Matthias ^a   Püllmann, Bernd ^a   Schmitt, Sébastien ^a  

^a F HOFFMANN LA ROCHE LTD   (Switzerland)

Author keywords

4H 1,2,4 oxadiazol 5 one; Combinatorial chemistry; Suzuki coupling; Triazolopyridine derivatives

Indexed keywords

SYNTHESIS (CHEMICAL);

COMBINATORIAL SYNTHESIS;

ORGANIC COMPOUNDS;

2 AMIDO 5 MORPHOLINO 8 METHOXYTRIAZOLOPYRIDINE DERIVATIVE; 4H [1,2,4]OXADIAZOL 5 ONE; ADENOSINE RECEPTOR; ADENOSINE RECEPTOR BLOCKING AGENT; OXADIAZOLE DERIVATIVE; RECEPTOR SUBTYPE; TRIAZOLOPYRIDAZINE DERIVATIVE; UNCLASSIFIED DRUG;

AMIDATION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; COMBINATORIAL CHEMISTRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; RECEPTOR BLOCKING; SYNTHESIS;

EID: 0042238086     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-40874     Document Type: Article

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