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filingDate 2010-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e91ba4a5fea09616fd38512f402c6109
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publicationDate 2010-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100971371-B1
titleOfInvention Method for preparing barleyconazole using a novel intermediate
abstract The present invention relates to a method for preparing boriconazole of formula (1), and more particularly, to lipomaski coupling reaction of a ketone compound of formula (4) with a pyrimidine derivative of formula (5) to obtain a formula (3), and substituted halo and jade The sulphonyl is reacted with hydrogen or a hydrogen donor under a palladium catalyst to prepare racemate voriconazole of formula (2), which is then optically partitioned through a suitable optically active acid to yield high yield of voriconazole of formula (1) having high optical purity. And to a method of manufacturing economically. [Formula 1]
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