http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2186023-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b09f893b262cefd50c5e76c4b85d1c0a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D241-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04
filingDate 1995-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06cfa9a9cf85dfb30a8881b6f8ec88d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53eedee8068ceddaefe2bb52a0327d85
publicationDate 1995-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2186023-A1
titleOfInvention Process for preparing 2-piperazine carboxylic acid derivatives
abstract The invention concerns a process for preparing 2-piperazine carboxylic acid amides of general formula (I): (I) wherein a piperazine carboxylic acid, N-acylated with a halogenating agent to form a piperazine carboxylic acid anhydride of general formula (IV): (IV) is cyclized and finally converted into the end product (I) with an amino component. The 2-piperazine carboxylic acid amides of general formula (I) are lnter alia valuable intermediate products for preparing orally active HIV-1 protease inhibitors.
priorityDate 1994-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 22.