http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6987189-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-70
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D419-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-00
filingDate 2004-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24ac398c76c3e14fae68a6d0753ddba0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31e45d13b269ae003a1f4df3027b99ce
publicationDate 2006-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6987189-B2
titleOfInvention Short synthesis of pyridine-based pharmaceutical intermediates
abstract A method of making a compound of Formula VI: n nwherein Tr is a triphenyl group; R 1 , R 2 and R 3 are each independently selected from the group consisting of H, C1–C4 alkyl, C1–C4 alkoxy, aryl, heteroaryl, and arylalkyl; R 4 is C2–C6 alkyl, and R 5 and R 6 are each independently H or C1–C4 alkyl, involves the step of reacting a compound of Formula V: n nwith Tr-OH to produce a compound of Formula VI. The compounds of Formula VI are useful as intermediates in the manufacture of antibiotic agents. Methods of making compounds of Formula V, and intermediates made or used in the foregoing methods, are also described.
priorityDate 2001-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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