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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-66
filingDate 1997-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc8612094babedbdd74ce41b99cb7c9d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a63550f7b7bca5932a200ef48d02e6b
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publicationDate 1998-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5817823-A
titleOfInvention Method for synthesizing 2-substituted imidazoles
abstract The present invention is a method of preparing 2-substituted imidazoles from readily available imidazoles having a leaving group in the 2-position, by alkylating the imidazole under mild conditions to afford a 3-N-alkylated imidazolium salt; and coupling the imidazolium salt with a nucleophile also under mild conditions to afford a 2-substituted 3-N-alkylated imidazolium salt. The reaction product can optionally be isolated and purified. The 2-substituted 3-N-alkylated imidazolium salt is hydrolyzed to afford a 2-substituted imidazole. Alternatively, the imidazole is coupled with a nucleophile in the presence of fluoride ion to provide a 2-substituted imidazole.
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Total number of triples: 503.