http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61126061-A

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filingDate 1984-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_934b5507d895ea200465b24625558be5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_156db00e2d809bd00983d9dfed3f70f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58130fe647e27e142b22ad2c2d0e4196
publicationDate 1986-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61126061-A
titleOfInvention Novel condensed benz(thio)amide, their preparation and drug containing same
abstract NEW MATERIAL:A compound of formula I [A is single bond, methylene, ethyl ene, vinylene; B is 4W8-membered hydrocarbon ring which may be substituted with O, N, S; T is O, S; R 1 is formula II (R 5 , R 6 are H, halogen), alkyl; R 2 is H, 1W6C alkyl; R 3 is H, halogen, hydroxyl; when B forms a ring, R 4 is the formula: -U-(CH 2 ) n -COOR 8 (U is O, S; R 8 is H, 1W6C alkyl; n is 0, 1W10)], and its non-toxic salts. n EXAMPLE: 7-(p-Hexyloxybenzoyl)amino-2-(r-tetrazolyl)benzofuran. n USE: Leucotriene antagonist, phospholipase inhibitor. n PREPARATION: A carboxylic acid of formula III or its corresponding dithionic acid is allowed to react with an amine of formula IV to form an amide bond, when needed, saponified to give a compound of formula I. n COPYRIGHT: (C)1986,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100686695-B1
priorityDate 1984-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 53.