http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0005980-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-60
filingDate 1979-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_626a6de09b545d65845f80efc9255223
publicationDate 1979-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0005980-A2
titleOfInvention Derivatives of substituted N-alkyl imidazoles, their preparation and these compounds for pharmaceutical use
abstract Derivatives of substituted N-alkyl imidazoles of the formula n<CHEM>n wherein R<1> is phenethyl and R<2> is phenyl, each of said phenethyl or phenyl independently being unsubstituted or substituted in the phenyl ring by from 1 to 3 substituents selected from the group consisting of halo, lower alkyl or lower alkoxy with the proviso that at least one of R<1> and R<2> be substituted by lower alkoxy; X is oxygen or sulfur; and the antimicrobial acid addition salts thereof are useful as antifungal, antibacterial and antiprotozoal agents. They can be prepared by etherification or thioetherification of the corresponding compounds having -OH in place of -XR<2>; or by reaction of R<1>CH(Y)CH2SR<2> and or R<1>CH(SR<2>)CH2Y with imidazole, wherein Y is a leaving group.
priorityDate 1978-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 585.