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filingDate 1981-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99f5079ed3892951047957564b5f6dcc
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publicationDate 1982-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0045251-A1
titleOfInvention Thiazolo(3,2-a)pyrimidine derivatives, their preparation and pharmaceutical compositions containing them
abstract - soit R est phényle ou alcoyle non substitué ou substitué par 1 à 3 halogènes, alcényle (2 à 4 C), cyclohexyle (3 à 6 C) et R 1 est hydrogène, ou bien R et R 1 , identiques ou différents, sont phényle ou alcoyle non substitué (1 à 4 C) ou forment ensemble un alcoylène (4 ou 5 C) et R 2 et R 3 , identiques ou différents sont hydrogène ou alcoyle (1 à 4 C), - soit R=R 1 =H et R 2 et R 3 sont l'un hydrogène et l'autre alcoyle (1 à 4 C) ou bien sont chacun alcoyle (1 à 4 C). New derivatives of general formula (I) in which: - either R is phenyl or alkyl unsubstituted or substituted by 1 to 3 halogens, alkenyl (2 to 4 C), cyclohexyl (3 to 6 C) and R 1 is hydrogen, or else R and R 1 , identical or different, are phenyl or unsubstituted alkyl (1 to 4 C) or together form an alkylene (4 or 5 C) and R 2 and R 3 , identical or different are hydrogen or alkyl (1 to 4 C), - either R = R 1 = H and R 2 and R 3 are one hydrogen and the other alkyl (1 to 4 C) or else are each alkyl (1 to 4 C). n n n These new derivatives are particularly active as anti-rheumatic and anti-allergic.
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