http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-385918-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d669af06cb2abbcd6823699582a97002 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C233-34 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-43 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-165 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-215 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C219-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C225-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C225-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-10 |
| filingDate | 1970-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1973-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-385918-A1 |
| titleOfInvention | PROCEDURE FOR THE PREPARATION OF NEW SUBSTITUTED BIS-ARILALCOHYLAMINES ACILDERIVATES. |
| abstract | Procedure for the preparation of new acylarivates of substituted bis-arylalcohil-amines of the general formula ** (See formula) ** in which Ar is a phenyl or naphthyl radical, Y means an optionally substituted alcoholic group based on 1 to 4 carbon atoms; means an acyloxy, acyloxyalkoxy, acylamino or acylalkyl amino [-N (alcoholic) (acyl)] group; R4 means hydrogen or a low molecular weight alcohol group, R5 means hydrogen, a low molecular weight alcohol group or an acyl group and R2, R3, R6 and R7, which are the same or different, mean hydrogen atoms, halogen atoms, hydroxy, low molecular weight alkoxy groups, acyloxy, amino, alkoxylamino, dialkoxylamino, acylamino, nitro, low molecular weight alcohol, low molecular weight halogenoalkoxy, such as for example trifluoromethyl and low molecular weight alcoholyl groups and in which the groups acyl are derived from fatty acids with 2 to 10 saturated or unsaturated, straight or branched chain carbon atoms, optionally substituted by halogen atoms, hydroxy groups, acylated hydroxy groups, oxo groups, low molecular weight alkoxy groups or phenyl radicals, the phenyl radicals may also be substituted by alcohol groups with 1 to 6 carbon atoms, alkoxy groups with 1 to 6 carbon atoms, hydroxy groups thus as halogen atoms, of benzoic acids optionally substituted one or more times by halogen atoms, hydroxy groups, acylated hydroxy groups, low molecular weight alcohol groups or low molecular weight alkoxy groups or low molecular weight aliphatic semi-esters of carbonic acid or of the phenylsemi-ester of carbonic acid, as well as its salts, its optically active isomers or diastereoisomers, characterized in that, in a manner known per se: a compound of the general formula is reacted ** (See formula) ** with a compound of the general formula ** (See formula) ** in which the symbols Ar, Y, as well as R1 to R7 have the meanings indicated above, with formaldehyde or substances that supply formaldehyde; and optionally in the obtained compounds one or more oxo groups are reduced to hydroxy groups and/or optionally other oxy or amino groups are acylated. (Machine-translation by Google Translate, not legally binding) |
| priorityDate | 1969-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 55.