http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1554255-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-47
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-46
filingDate 2003-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55325d6bc3a043ea9e9325dac78ff836
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4058b13f176c8c566074f8bab0b67913
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23590bd3888e228b46f00873d60d25d6
publicationDate 2005-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1554255-A1
titleOfInvention Method for the production of 2-amino-4-chloro-6-alkoxypyrimidines
abstract The invention relates to a method for producing 2-amino-4-chloro-6-alkoxypyrimidines by reacting 2-amino-4,6-dichloropyrimidine with an alkali alcoholate or a mixture of alkali hydroxides and an alcohol in a polar aprotic solvent (mixture), whereupon the solvent is distilled off to > 30 percent and the product is precipitated by adding water during or following the distillation process. The inventive method, in which especially acetone is used as a polar aprotic solvent and which can be carried out at temperatures between 5 and 60 °C, allows 2-amino-4-chloro-6-alkoxypyrimidines and above all 2-amino-4-chloro-6-methoxypyrimidine to be produced in a particularly economical and environmentally friendly manner while obtaining high yields and a very distinctive purity.
priorityDate 2002-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 32.