http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S55153782-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0d6256baf554e46784d8daa478a2ddc6
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D337-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-38
filingDate 1979-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_898d1cc69e49be8d9eb6a3ece37a7549
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dad50da82e193beec3fb39a40afea230
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_226a07b00352c45bc1dc3d9501d91b4c
publicationDate 1980-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S55153782-A
titleOfInvention Dibenzo (b,f) thiepin derivative
abstract NEW MATERIAL:A dibenzo [b, f] thiepin derivative of formula I [R is H or 2-(2- hydroxyethoxy)ethyl group]. n EXAMPLE: 2-(8-Methyl-10,11-dihydro-11-oxodibenzo[b,f]thiepin-2-yl)propionic acid. n USE: An anti-inflammatory, analgesic, and antipyretic agent having a powerful pharmacological effect and remarkably improved safety. n PROCESS: A novel compound of formula II is cyclized by the well-known method to give the compound of formula I (R is H). The resulting compound or its reactive derivative is esterified with a compound of formula III (X is halogen of atomic number ≥17) by the conventional method to form the compound of formula I [R is 2-(2-hydroxyethoxy)ethyl group]. The compound of formula II can be prepared from the compounds of formulas IV and V (R' is 1W6C alkyl group). n COPYRIGHT: (C)1980,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0129793-B2
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priorityDate 1979-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 25.