http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1217773-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6b460b6e95e64228f98a7ffc6bde16de
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-60
filingDate 1983-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_442d0c51c1f7f042b4cfb701b4c056ff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52b164016f40770bd2cdc4e819b79a07
publicationDate 1987-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1217773-A
titleOfInvention L-n-n propyl-pipecolic acid-2,6-xylidide and method for preparing the same
abstract L-N-n-PROPYLPIPECOLIC ACID-2,6-XYLIDIDE AND METHOD FOR PREPARING THE SAME Abstract The local anesthetic, L-N-n-propylpipecolic acid-2,6-xylidide, namely: This compound is prepared by chlorinating L-pipecolic acid to yield the acid chloride, namely L-pipecolic acid chloride. The acid chloride is then reacted with 2,6-xylidine to yield L-pipecolic acid-2,6-xylidide. The L-N-pipecolic acid-2,6-xylidide is then propylated to yield the L-N-n-propylpipecolic acid-2,6-xylidide, which is a potent local anesthetic for mammals including man and is of rela-tively low toxicity.
priorityDate 1983-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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