http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103804315-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_53b4d53983adbf56dd0e7d0bf96f8ce5
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10
filingDate 2014-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00a0c096d17ed7fb9431ab5e96939fc6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c072966715e54ae4cfcec7f67020df4f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4573fe0d68db1d6d05ff3d503de9a43
publicationDate 2014-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103804315-A
titleOfInvention A kind of preparation method of 5-aminomethyl oxazolidinone compound
abstract The invention discloses a preparation method of 5-aminomethyloxazolidinone compound (I), which uses racemized or optically active 3-halo-2-hydroxypropylaniline compound as a starting material, React with the corresponding chloroformate or Boc anhydride under appropriate solvent and alkaline conditions to get 3-halo-2-hydroxypropyl-1-acylanilide compound (3), compound 3 can be combined with Ammonia undergoes ammonolysis reaction to obtain racemic or optically active 5-aminomethyloxazolidinone compound (I); In the formula: R 1 represents morpholinyl or 3-oxo-4-morpholinyl; R 2 represents H or F; the compound is a racemate, (S)-optical isomer or (R)-optical isomer .
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110054621-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105130976-A
priorityDate 2014-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012140061-A1
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Total number of triples: 23.