http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-519691-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
filingDate 2000-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a72a98a6daf04bf4f08edce59c4056e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03c57ed2187d381023aabfe5fcd1914e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_839067aac7482f0136fc0c3da3bce020
publicationDate 2004-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-519691-A
titleOfInvention Process for the preparation of pyrazolo[1,5-B]pyridazine derivatives
abstract A process for the preparation of a compound formula (I), which comprises oxidizing under conventional conditions the corresponding formula (II), in regards to formula(I) where, R0 is a halogen, C1-6alkyl, C1-6alkoxy, C1-6alkoxy substituted by one or more fluorine atoms, or O(CH2)nNR4R5; R1 and R2 are independently selected from H, C1-6alkyl, C1-6alkyl substituted by one or fluorine atoms, C1-6alkyoxy, C1-6 hydroxyalkyl, SC1-6alkyl, C(O)H, C(O) C1-6alkyl, C1-6alkylsulphonyl, C1-6alkoxy substituted by one or fluorine atoms, O(CH2)nCO2C1-6alkyl, O(CH2)nSC1-6alkyl, (CH2)nNR4R5, (CH2)nSC1-6alkyl or C(O)NR4R5, (CH2)nSC1-6alkyl or C(O)NR4R5; R3 is C1-6alkyl or NH2; R4 and R5 are independently selected from H, or C1-6alkyl or together with the nitrogen atom to which they are attached, form a 4-8 membered saturated ring; and n is 1-4; where R0 and R3 are as defined for formula (I) below.
priorityDate 1999-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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