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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G02B23-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02B23-12
filingDate 1969-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_540b9afd6497980b40e7a1722a04e0ee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a187feb6ecabcfeda3aa7cfde53b9911
publicationDate 1972-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-521306-A
titleOfInvention Process for the preparation of tricyclic compounds
abstract (A) Cpds. of general formula (I) Including salts, and stereoisomers of I. R' = H or Me R = Me or MeCO (B) N-oxides of I (R' = Me). Antidepressants, adrenolytics, antihistamines, and local anaesthetics, with low toxicity and slight anticholinergic activity. 1-Methyl-10,11-dihydro-(3-dimethylamino-propylidene) 5H-dibenzo(a,d)cycloheptene (39.5 g), was hydrogenated at 25 deg./1 atm., over Pt2O (3 g.) in AcOH (400 ml). The mixture was filtered, evapd. and the residue distilled, giving the 3-dimethylaminopropyl deriv., b.p.140 deg./0.01 mm. (Hydrochloride m.p.181-3 deg., from Et2O-EtOH).
priorityDate 1969-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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