http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-10140269-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d669af06cb2abbcd6823699582a97002
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-54
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-54
filingDate 2001-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e40c6e095252b87440825c50fe3ea4b3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6f165add4af6faadb9a146d5eed24db
publicationDate 2003-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-10140269-A1
titleOfInvention Process for the preparation of 4,6-dihydroxypyrimidine
abstract The invention relates to a process for the preparation of 4,6-dihydroxypyrimidine by reacting malonic diester with formamide and alkali alcoholate. The malonic acid ester, alone or simultaneously with the total amount or a partial amount of the formamide, is added in portions or continuously with temperature control to the alkali alcoholate presented as a solution or suspension in an alcohol alone or together with the total amount or the remaining partial amount of the formamide. A temperature of 102 to <120 ° C. is then set for 10 to <60 minutes. Working up after the holding time in the temperature range mentioned is then carried out in a manner known per se.
priorityDate 2001-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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