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filingDate 2007-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbe4063a2cd096571e3ca01fb8e3fd14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8450bdd50c8b922120190c83a42832e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_013c71edb5d8bb59ab23444dcc63da53
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae022148b02ea5711ae9d5bcdb194e4c
publicationDate 2011-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8076479-B2
titleOfInvention Process and intermediates for the synthesis of (3-alkyl-5-piperidin-1-yl-3,3a-dihydro-pyrazolo[1,5-a]pyrimidin-7-yl)-amino derivatives and intermediates
abstract Disclosed is a process for the synthesis of compounds of Formula I n nby sequentially aminating, first with a primary amine and then with a secondary amine, an intermediate compound of the structure of Formula E1,n n nwherein R 1 is a linear, branched, or cyclic alkyloxy functional group of the structure (—R 2a —OH), R 2a is a linear, branched or cyclic alkyl group, R 2 is a linear, branched or cyclic alkyl group, and R 3 is an alkylene-heterocycle, said process comprising forming intermediate compound of Formula E1 by reacting, in a refluxing reaction solvent selected from alcohols having 5 or less carbon atoms and mixtures of two or more thereof, a methanol solution of a salt of a 4-alkyl-3-amino-pyrazole compound of Formula C1,n n nwith a diamidization reagent selected from dimethylmalonate, monomethylmalonyl-chloride, and malonyl dichloride in the presence of a Lewis base having sufficient proton affinity to abstract a proton from the 1-position nitrogen on the pyrazole ring.
priorityDate 2006-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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