Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ca5e90b147553aa5db872967761c7d37 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-445 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-572 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-08 |
filingDate |
1989-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3ae23d7f0773e83626431fe8195a62b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11e74b906ff3ff8a6cb251342cf50979 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76a9df1551c07b481559f59a81367cc1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e907fd4b6d047d1d2672121b617ccd8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25e765b604eb0067e3556d6304ecaf6b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_29f704f58463285f62467497c5fe1cfc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_706616fe53d8ea0efc6b432ef0727c18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9a2cff20f335cde5f28e4ff44978e23 |
publicationDate |
1990-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
JP-H02178-A |
titleOfInvention |
Novel aminoalkylbenzene derivative |
abstract |
NEW MATERIAL:The compound of formula I [Y is (OH-substituted) 1- pyrrolidinyl, 1-piperidinyl or 1-perhydroazepinyl; R 1 is H or lower alkyl; Z is =N-CN or =CH-NH 2 ; R 2 is lower alkyl; m is 0 or 1; n is integer of 1-4; group of formula II is bonded to meta- or para-site relative to the group of formula III] or its salt. n EXAMPLE: N-cyano-N'-methyl-N'-[4-[3-(1-piperidinylmethyl) phenoxy]-cis-2- butenyl] guanidine. n USE: An antiulcer agent having excellent gastric inhibitory action originated from histamine H 2 receptor antagonistic action. n PREPARATION: A compound of formula I (Z is =N-CN) is produced by reacting a compound of formula IV or its salt with a compound of formula V (R 4 is lower alkyl) and reacting the resultant compound of formula VI or its salt with a compound of formula R 2 -NH 2 . n COPYRIGHT: (C)1990,JPO&Japio |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022034121-A1 |
priorityDate |
1989-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |