http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2997536-B2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-06
filingDate 1990-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5eb25fb6ec988d8d08590872fe86539c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1092cdf08189f9e65aebedc08b62937
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publicationDate 2000-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2997536-B2
titleOfInvention Pantothenic acid derivative
abstract NEW MATERIAL:A compound of formula I {R<1> and R<2> are each H or protective group for OH; R<3> is (aromatic group-substituted)5-25C monovalent aliphatic hydrocarbon group or NH-R<4> [R<4> is (aromatic group-substituted)5-25C monovalent aliphatic hydrocarbon group); (m) is 2 or 3; (n) is 1-4}. EXAMPLE:1-Hexanoyl-4-{1-oxo-3-[N-(1-oxo-2,4-diacetoxy-3,3-dimethylbutyl) amino]propyl}piperazine. USE:Having inhibitory activity for acyl CoA-cholesterol-acyl transferase, thus useful for the therapies for hyperlipemia, arteriosclerosis, etc. PREPARATION:The objective compound of the formula I can be obtained by reaction between (A) a compound of formula II (R<11> and R<12> are each protected OH) and (B) a compound of formula R<3>-COZ<1> (Z<1> is H, halogen, alkoxy, etc.) or formula R<4>-NCO using, as necessary, a catalyst or reaction promoter in a solvent such as methylene chloride at temperatures ranging from -78 deg.C to the boiling point of the solvent.
priorityDate 1989-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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