Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2e5edd48190cba3fa70dd3975efd9831 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-55 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 |
filingDate |
1969-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae808512072124a3b84238cf428eed93 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5957919c64ac749123a1fee02f3f163a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f499f67de478e9b986c85eb4cac1279 |
publicationDate |
1971-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
DE-1936670-A1 |
titleOfInvention |
New diallylaminoalkanoylamides |
abstract |
Novel diallylaminoalkanoylamides of formula (I): (where R1 is H or 1-4C alkyl; R2 and R3 are independently H or halogen; Y is =CH- or N; A is methylene or ethylene). Prefd. cpds. include 11-diallylaminoacetyl-5,11-dihydro-5-methyl-6H-pyrido- 2,3-b 1,4 benzodiaze-pin-6-one. Cpds. pref. prepd. by reacting a haloalkanoyl of formula (I) (where -N(CH2-CH=CH2)2 is replaced by halogen) with a diallylamine and opt. converting to its (in)organic acid addn. salts. Cpds. inhibit ulcers. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0393529-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5620974-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5366972-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0086980-A1 |
priorityDate |
1968-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |