Straightforward access to ethyl 3-aminofuropyridine-2-carboxylates from 1-chloro-2-cyano- or 1-hydroxy-2-cyano-substituted pyridines

Synthesis

Volumn , Issue 20, 2007, Pages 3247-3251

  Cailly, Thomas ^a   Lemaître, Stéphane ^a   Fabis, Frédéric ^a   Rault, Sylvain ^a  

^a CENTRE D ETUDES ET DE RECHERCHE SUR LE MÉDICAMENT DE NORMANDIE   (France)

Author keywords

Aryl alcohols; Cyclizations; Fused ring systems; Nitriles; Nucleophilic aromatic substitutions

Indexed keywords

ARYL ALCOHOLS; FUSED-RING SYSTEMS; NITRILES; NUCLEOPHILIC AROMATIC SUBSTITUTIONS;

ALCOHOLS; CYCLIZATION; ISOMERS; NITROGEN COMPOUNDS; PYRIDINE; SYNTHESIS (CHEMICAL);

REACTION KINETICS;

2 CHLORO 3 CYANOPYRIDINE; 2 CYANO 3 HYDROXYPYRIDINE; 4 CHLORO 3 CYANOPYRIDINE; 4 CYANO 3 HYDROXYPYRIDINE; 4 IODO 3 CYANOPYRIDINE; CARBOXYLIC ACID DERIVATIVE; ETHYL 3 AMINOFURO[2,3 B]PYRIDINE 2 CARBOXYLATE; ETHYL 3 AMINOFURO[2,3 C]PYRIDINE 2 CARBOXYLATE; ETHYL 3 AMINOFURO[3,2 B]PYRIDINE 2 CARBOXYLATE; ETHYL 3 AMINOFURO[3,2 C]PYRIDINE 2 CARBOXYLATE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLIZATION; ISOMER; ONE POT SYNTHESIS; STEREOCHEMISTRY;

EID: 35548930654     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990810     Document Type: Article

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