http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1299500-A3

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8ef7079abdd69a7a1996c43f08fe1111
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C5-00
filingDate 1983-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e80204efe6142377973818cdbc6e7b40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a13506501709c1a92d225ad3ef2a05c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e089eaab57e67575a8f7e87919526b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e52ee793b5819f08681841e5c4234afa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a8332113cfc6e15aa5708ba1270a1ff
publicationDate 1987-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1299500-A3
titleOfInvention Method for producing derivatives of 1-aryl-2-aminoethanol-1
abstract The invention relates to amino alcohol derivatives, in particular 1-aryl-2-aminoethanol-1 (AE) of the general formula (I): X-Ar-CR (OH), jR, where Ar is phenyl or naphthyl, benzo-1,3- dioxane, thienyl; X - And, C1, Br, lower alkyl, alkoxyl, NOj; K - lower alkyl, H; K and RJ - H, lower alkyl, phenyl, phenylethyl, which are used for the synthesis of biologically active compounds. The purpose of the invention is the creation of a universal method, providing a wider range of compounds of the specified class. The synthesis of AE includes the steps of: a) reacting a sulfide of the general formula (II): R-SCHj, where is n-alkyl, with dimethyl sulfate in a water-immiscible organic solvent (); b) adding to the reaction mixture first an alkali in the presence of a catalyst, tetrabutylammo bromide, and then a carbonyl compound of formula (III): X - Ar - CR, (0), where X, Ar, R, are indicated above; c) removing water and / or part of an organic solvent and treating the residue with an amine of the general formula (IV):, where F, and F are as above. The method provides AE in the form of hydrochloride with a yield of 60-75%. with (oh w x with sp about o see
priorityDate 1982-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410567559
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6858
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415736820
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394837
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419517945
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71359729
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419595498
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID74236
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559213
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557048
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6497
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559212
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524338
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID77289
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67490
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID259
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6385
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID77287
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450067302
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512847
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458427722
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID260
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457814461
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419550801
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID148919763
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523150
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394722
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412222544
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394761
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10315
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20466330
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410578252
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11101
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559516
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6195
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412222538
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419582769
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811

Total number of triples: 63.