http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0105692-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D327-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D327-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-00
filingDate 1983-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1988-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0105692-B1
titleOfInvention 6-h-dibenz(b,e)(1,4)oxathiepin derivatives and their preparation
abstract 6-H-Dibenz[b,e][1,4]oxathiepin derivatives of the formulae I and IA are novel. They can be used in the treatment and control of allergic conditions such as allergic asthma. <CHEM> They are made by reducing the corresponding compound in which the (CH2)nOR<4> residue is replaced by a (CH2)n-1COOH residue. In the formula n is 1, 2, 3 or 4, Z is thia, sulfinyl or sulfonyl; each of R<1>, R<2> and R<3> is H, halogen, NH2, alkyl, alkylthio, alkylsulfinyl, alkylsulfonyl, CF3, CF3S, CN, NO2, alkylamino, dialkylamino, alkoxy, alkanoyl, aralkyl, or hydroxyalkyl, or R1 and R2 together represent polymethylene, possibly oxo or hydroxy substituted; and R4 is H, acyl, alkylaminoacyl, alkylcarboxy, alkylcarbamoyl, alkylcarbamoylacyl or acyloxyalkyl.
priorityDate 1982-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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