http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2341307-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bee8b2c674d7ec672688001f27aa95fe
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-60
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-60
filingDate 1973-08-16^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6c7692140eb4ded683542bb07e7ba8e
publicationDate 1975-02-20^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2341307-A1
titleOfInvention ACYLOXYHYDROXY-INDOLE COMPOUNDS AND METHOD FOR THEIR PRODUCTION
abstract Benzo g indole-3-carboxylic acid derivs. of formula (I) (where R1 and R2 are alkyl, cycloalkyl aral, aralkyl, alkoxyaryl or haloaryl, R3 is alkyl, aryl, aralkyl, alkoxy, aryloxy or aralkoxy, R5 is acyloxy, And Rx is H, alkyl, aryl, alkoxy, OH, acyl, halogen, or halo-substd. alkyl or aryl) e.g. 5-acetoxy-4-hydroxy-2-methyl-1H-benzo g -indole-3-carboxylic acid ethyl ester, are prepd. by reacting acyloxy-naphthoquinones of formula (II) with enamines of formula (III) in a solvent (the condensation being accompanied by migration of the acyl group of R5 to the hydroxyl group resulting from the adjacent oxo group) and if desired converting the resulting cpd. into its derivs. by acylation or saponification. Known similar cpds. have e.g. hypotensive and psychopharmacological activity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5985919-A
priorityDate 1973-08-16^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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