http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S62292777-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-352
filingDate 1986-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa50b96d0686fb4513690f914a6c31c4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a0ed056872066151bb9590056738abe
publicationDate 1987-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S62292777-A
titleOfInvention Fluorine-containing coumarones
abstract NEW MATERIAL:A fluorine-containing coumarone shown by formula I (R is 1W16C alkyl; R 2 , R 3 and R 4 are H, F, 1W5C alkyl or 1W8C fluoroalkyl; with the proviso that at least one of R 2 , R 3 and R 4 shows F or 1W8C fluoroalkyl). n EXAMPLE: 8-Iodo-2,2,5,7-tetramethyl-6-acetoxycoumarone. n USE: Useful as an agent for lowering cholesterol, a remedy for arteriosclerosis, etc. n PREPARATION: For example, as shown the reaction formula, a compound shown by formula II as a starting substance is simultaneously reacted with iodine and silver trifluoroacetate in a halogen solvent such as chloroform, etc., at room temperature and H at the 5-, 7- or 8-position is converted into iodine atom. Then the reaction product is reacted with a trifluoroalkyl iodide and copper and the reaction product obtained by the second process is hydrolyzed to give a compound shown by formula I. n COPYRIGHT: (C)1987,JPO&Japio
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priorityDate 1986-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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