http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012246255-A

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B59-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01T1-161
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K51-00
filingDate 2011-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_588bb6ddc9470ac12403138e7ef0ed98
publicationDate 2012-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2012246255-A
titleOfInvention Method for producing 11C-labeled amino acid analog and nuclear medicine diagnostic imaging agent
abstract An object of the present invention is to provide a method for producing an 11 C-labeled amino acid analog capable of easily producing an 11 C-labeled amino acid analog labeled with a radioisotope of carbon. A method of manufacturing a radioactive isotope in the production of labeled 11 C-labeled amino acid analogs 11 C-labeled amino acid analogs of carbon, in dimethyl sulfoxide solution (DMSO), R 1 (R 2) A first step S1 in which C═N—CH (CH 3 ) —COOR 3 , [ 11 C] H 3 X, and tetra-n-butylammonium fluoride (TBAF) are reacted, and the first step S1 Thereafter, a second step S2 in which a 1-2 M alkaline aqueous solution is added and reacted, and after the second step S2, a 1-2 M acidic aqueous solution is added and reacted to produce a 11 C-labeled amino acid analog. And 3 steps S3. [Selection] Figure 1
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113493392-B
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priorityDate 2011-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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