http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2327545-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-08
filingDate 1973-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57c6584d2b0e9ff9dbad22aca536825b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24e112d002021a433298aa56a8714643
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4928625e68c1ec09b0fbb1b94c485fe6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98d659772cf2ebaa16e7708771c6058e
publicationDate 1974-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2327545-A1
titleOfInvention TETRAHYDRO-V-TETRAZINE COMPOUNDS
abstract Cpds. of formula (I) (where R1 and R2 are 2-5C alkyl or 4-7C cycloalkyl, and R3 and R4 are H or lower alkyl, or R1 + R3 and R2+R4 are -(CH2)n- (n = 3, 4, 5 or 6) or -(CH2)2-X-CH2- (X = O or NR5, R5 being lower alkyl)) have biological activity; for example, in experimental animals they display activity on the central nervous system. (I) are prepd. by redn. of N-oxides of formula (II) (obtainable by reaction of 2 molecules of alpha-metallated nitrosamines) to the oxygen-free cpds. e.g. by treating with excess tiralkyl phosphite.
priorityDate 1973-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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