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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-56
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-56
filingDate 1994-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f375a589ac1834c7b525aaf4e0fc042f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b84efecc8ad8044895acee21188f0fa5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6cf029eb28d2b3551be2df56fce7457d
publicationDate 1994-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9424109-A1
titleOfInvention Indazole derivatives and antiviral drugs that contain them
abstract The present invention pertains to indazole derivatives of formula (I), methods of preparing them and drugs containing these compounds. The invention particularly pertains to indazole derivatives of formula (I), in which R is a phenyl ring or a carbocyclic ring with 7-15 C atoms or a heterocyclic ring, and the aforementioned rings may be substituted by C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkyl mercapto, amino, C1-C6 alkyl amino, di-C1-C6 alkyl amino, C1-C6 alkyl carbonyl amino, hydroxy, nitro, halogen, trifluoremethyl or azido, R1 is a hydrogen atom, a straight-chained or branched, saturated or unsaturated aliphatic group with 1-6 C atoms, R2 is C1-C8 alkyl, C2-C8 alkenyl, C4-C8 cycloalkyl, C3-C8 cycloalkenyl, X is an oxygen or sulfur atom, Y is a nitrogen atom or CR1, as well as their tautomers, enantiomers, diastereoisomers and physiologically tolerable salts.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107082763-A
priorityDate 1993-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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