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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-475
filingDate 1981-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccbfff221e0c34f4597ba9ac8ef95c2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42dc5d3b4e1a7bfed1385fe248b463af
publicationDate 1983-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1159055-A
titleOfInvention Use of vlb 3-(2-chloroethyl) carboxamide in treating neoplasms
abstract Abstract A pharmaceutical formulation which comprises as an active ingredient (VLB or 4-desacetyl VLB) 3-(2-chloroethyl) carboxamide or a pharmaceutically-acceptable acid-addition salt thereof with a pharmaceutically-acceptable carrier therefor. Processes for preparing the active ingredient include (1) hydrolyzing the corresponding spirooxazolidinedione, (2) reacting the carboxazide with 2-chloroethylamine, and (3) reacting the 3-(2-hydroxyethyl)-carboxamide with a reagent which facilitates the replace-ment of a hydroxy function with chlorine and a source of chlorine. The process may include the optional steps of deacetylating, acetylating; and salifying the free base formed by the first-mentioned process of hydrolysis.
priorityDate 1980-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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