http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014118357-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_67dd1f39f37bac4617e37d6d5c60aa8b |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 |
filingDate | 2012-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cdf91dc0b93ad1cc556e3847fd9221f4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cad9d315d66491a236feffe689bf0639 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_060ba00470f99d4612c45feedee22858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c91d10a20f937ed36055691d22ff335f |
publicationDate | 2014-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2014118357-A |
titleOfInvention | Process for producing substituted pyrazolopyrimidine compounds and intermediates thereof |
abstract | The present invention provides an industrially efficient production method of substituted dihalopyrazolopyrimidine compounds useful for the production of pharmaceuticals and the like. The method comprises reacting a specific 3-aminodiazole compound or a salt thereof with malonic acid or Meldrum acid or a salt thereof in the presence of a halogenating agent: (Wherein, ring A represents an optionally substituted heteroaryl), or a salt thereof. [Selection figure] None |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105061338-A |
priorityDate | 2012-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 89.