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filingDate 1980-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00d306beae502c5df036ebbf43109588
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be189ead9002c865add3406e834fa832
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26d72e47528358a0657a39aa9a15768f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6933701ac564cc66789f033f1d9e56d6
publicationDate 1985-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-234018-B2
titleOfInvention Method of 3,5-diammino-6-1,2,4-triazine derivatives making
abstract The present invention provides compounds of the formula (III):n or an acid addition salt thereof, wherein R 6 is chlorine, bromine, iodine, C 1 - 4 alkyl or trifluoromethyl, R 7 is hydrogen, halogen, C 1-4 alkyl or trifluoromethyl or R 6 and R 7 form a -CH=CH-CH=CH- group optionally substituted by a halogen atom or a C 1-4 alkyl or trifluoromethyl group, R 8 is hydrogen, halogen, C 1-4 alkyl or trifluoromethyl, R 9 is hydrogen, halogen, C 1-4 alkyl or trifluoromethyl, R 10 is hydrogen, methyl or fluorine and R" is amino, C 1-4 acylamino or di-substituted aminomethyleneamino provided that, at most, only two of R 7 ―R 10 are other than hydrogen and that R 7 ―R 10 are not all hydrogen when R 6 is chlorine. Also provided are pharmaceutical compositions containing compounds of the formula (III), the first medical use of compounds of the formula (III), a process for preparing such compounds and intermediates through which this process proceeds.
priorityDate 1979-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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