http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-235197-B1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a5216512c820a8524d117de905d60eed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2678584c4f8e2d70ca75a7e13f16cee3
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1984-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e89b166024b660fc6ffe8311522033d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08651df46b1e0056cda6e3b1320a85c7
publicationDate 1985-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-235197-B1
titleOfInvention Process for preparing 4,9-dihydro-3,9-dimethyl-4-oxo-1H-pyrazolo (3,4-b) quinolines
abstract The present invention relates to a new method of preparationn4,9-dihydro-3,9-dimethyl-4-oxo-1H-pyrazolo-n[3,4-b] quinolines, characterized in thatnalkylates 4,9-dihydro-3-methyl- disodium saltn-4-oxo-1H-pyrazolo [3,4-b] quinolines in dimethylformamidenwith methyl iodide at 0 ° Cnto 30 ° C, preferably at 20 ° C, barrelnthe reaction mixture is crystallized from methanol,nethanol or n-propanol, preferably ethanol,nand a mixture of 4,9-dihydro-1,3,9-trimethyl-4-oxo-1H-pyrazolo [3,4-b] quinolinesnand 4,9-n-dihydro-2,3,9-trimethyl-4-pxo-2H-pyrazolo · -n[3,4-b] quinolines are heated with the hydrochloridenpyridine at 200 to 240 ° C, preferablynat 220 ° C.
priorityDate 1983-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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