http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-192795-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4184
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-30
filingDate 1983-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91fbd84cea1eda90fdccf7ce3c769100
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff88dbb03bb64d2d7faea001f371159e
publicationDate 1987-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-192795-B
titleOfInvention Process for the elimination of 1-sulphonyl group of substituted benzimidazoles
abstract This invention concerns a process for removing a sulfonyl group from the 1-position of a benzimidazole to allow conversion of 2-amino-1,5-substituted-benzimidazole compounds into 2-amino-1,6-substituted-benzimidazole compounds. The 5-isomer is reacted with an alkali metal hydroxide or carbonate in an inert aqueous organic solvent system. The reaction mixture is acidified to precipitate the base and form the intermediate benzimidazole tautomer. The intermediate is then reacted with a sulfonyl acylating agent or a haloalkyl isothiocyanate to form a mixture of 2-amino-1,5(6)-substituted-benzimidazole compounds. This invention also concerns the process for removing a sulfonyl group from the 1-position of a benzimidazole to allow conversion of 2-amino-1,6-substituted-benzimidazole compounds into 2-amino-1,5-substituted-benzimidazole compounds.
priorityDate 1982-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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