http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-268630-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a8095fcbc14f32f140efa46074f127f1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e328a2ab7281bb7472ead0a2749edaf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f0f5d3902e8f1ca5a026f5a70fc3ec47
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D337-14
filingDate 1988-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5eaa24f893d490d714a73ca7ca4a3787
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1fffb19a58b9e509a0014cec12bf1095
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_74438a7b35c201af5d5756343c9eacdd
publicationDate 1990-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-268630-B1
titleOfInvention Process for the preparation of 6- (aminoalkoxy) dibenxo / b, f-thiepine-10 (11H) -ones and their hydrochlorides
abstract The solution is in the field of drug synthesis,nHis object is the way of preparationn2-dimethylamino (or piperidino) ethyl ethersnand 3-dimethylamino (or piperidino) propyl ethersnderived from 6-hydroxydibenzo [b, f] thiepin-10 (11H) -onenandnits 2-chloroacetate as well as theirnhydrochlorides, said antimicrobial agentsnefficiency in testeoh innin vitro and are therefore potenoic chemotherapeutics.nBesides, they still havensome other pharmacodynamics are preferrednProperties. Their preparation according to the solutionnit consists in the reaction of the sodium saltsnof phenol ketones with 2-dimethylaminon(or piperidinoethyl chloride orn3- dimethylamino (or piperidine propyl chloridenin boiling ethanol in the presence ofnsodium ethoxide. Obtained basesnwith neutralization with hydrochloric acidnor with hydrochloric acid.
priorityDate 1988-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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