http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2290402-C1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_12a0dc58f7c4e7c374fc78bd334260c5
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-58
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-72
filingDate 2005-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0423b7ba1cace98315eee62ec74ea6e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd62a13f3e448794e6c5cbd442553b19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee7e27a2200bebb2c54271d1be2e9fff
publicationDate 2006-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2290402-C1
titleOfInvention Method for preparing 2,5,7,8-tetramethyl-2-(2'-carboxyethyl)-6-acetoxychromane as precursor of alpha-sens
abstract FIELD: organic chemistry, chemical technology, medicine. n SUBSTANCE: invention relates to a method for synthesis of biologically active substances, namely to a method for synthesis 2,5,7,8-tetramthyl-2-(2'-carboxyethyl)-6-acetoxychromane (α-SENS). Method involves the condensation reaction of trimethylhydroquinone with linalool in the boiling n-octane medium in the presence of p-toluenesulfoacid or (+)-camphor-10-sulfoacid as a catalyst for 3 h in the mole ratio trimethylhydroquinone : linalool : catalyst = 1:1:0.1, respectively. Then the method involves the acetylation reaction of the synthesized substance with acetic anhydride in pyridine medium at room temperature for 0.5 h, ozonization in acetone medium in the presence of Ba(OH) 2 , oxidation with the Johns reagent in acetone medium and the following isolation by column chromatography on silica gel. This compound is acetate derivative of the main metabolite of α-tocopherol, i. e. α-SENS that shows the high effectiveness in treatment of the central nervous system diseases. n EFFECT: improved method of synthesis, valuable medicinal properties of compound. n 1 cl, 2 ex
priorityDate 2005-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID819166
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452407218
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID819310
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID33438

Total number of triples: 314.