http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1513843-B1

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filingDate 2003-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1631c4c62eef5faa40949d4d9112b9c6
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publicationDate 2007-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1513843-B1
titleOfInvention Pyrazolopyrimidines and the use thereof for controlling harmful organisms
abstract 7-Amino-6-aryl-pyrazolo-(1,5-a)-pyrimidine derivatives (I) are new. Also new are halo-, hydroxy- or dihydroxy-pyrazolopyrimidine derivative intermediates (II). Pyrazolopyrimidines of formula (I) and their acid addition salts (in the case where R1 = amino) are new. R1 = NH2 or OH or alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkoxy, mono- or dialkylamino, alkenylamino, alkynylamino, cycloalkylamino, N-cycloalkyl-N-alkylamino, alkylideneamino or heterocyclyl (all optionally substituted); R2 = H or alkyl, alkenyl, alkynyl or cycloalkyl (all optionally substituted); or NR1R2 = optionally substituted heterocycle; R3 = optionally substituted aryl; X1 = H or halo; X2 = halo, CN, NO2, haloalkyl, CHO, alkoxycarbonyl, alkylcarbonyl, hydroxyiminoalkyl or alkoxyiminoalkyl. Independent claims are also included for: (1) preparation of (I); (2) new halo-, hydroxy- or dihydroxy-pyrazolopyrimidine derivative intermediates of formula (II); and (3) preparation of (II). Q1 = halo and Q2 = X1; or Q1 = OH and Q2 = H or OH.
priorityDate 2002-05-29-04:00^^<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: 1659.