http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CO-5210949-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d4b619a689f14cadd8e0c6298d60f7e3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 1999-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea022aba6f0937095753878d434820f8
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publicationDate 2002-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CO-5210949-A1
titleOfInvention TRIFLUOROMETILALQUILAMINOTRIAZOLOPIRIMIDINAS FUNGICIDAS
abstract An optically active 7- (1,1,1-trifluoroalc-2-ylamino) -triazolopyrimidine of formula l <EMI FILE = "99059982_1" ID = "1" IMF = JPEG> in which R1 represents a C1-6 alkyl group; CH * indicates a chiral carbon atom; Hal represents a halogen atom, L1 to L5 each independently represents a hydrogen or halogen atom or an alkyl, alkoxy or nitro group, characterized in that the enantiomeric excess of (S) -enantiomer is at least 70%. A process for the preparation of an optically active compound of formula I as defined in any of the preceding claims comprising Treating a compound of formula ll <EMI FILE = "99059982_2" ID = "2" MFI = JPEG > in which L1 to L5 and Hal are as defined in claim 1 and with an optically active amine of formula III <EMI FILE = "99059982_3" ID = "3" IMF = JPEG> in which R1 and R2 are as defined in claim 1, M represents a hydrogen atom or a free or complexed metal atom, and the e Enantiomeric xcess of the (S) -enantiomer is at least 70%, at a reaction temperature in the range of 0 ° C to 70 ° C, and in the presence of a base.
priorityDate 1998-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Predicate Subject
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Total number of triples: 26.