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filingDate 2003-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47034432824c781d7cc8785d6e5d70b9
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publicationDate 2009-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-10346228-B4
titleOfInvention Preparation of [18 F] Fluorinated Aromatic L-Amino Acids
abstract Process for the preparation of [ 18 F] fluorinated aromatic L-amino acids, comprising the following steps: (1) providing the L-enantiomeric compound shown below in a suitable reaction medium: wherein R 1 and R 2 are suitable protecting groups for OH groups, if a hydroxyamino acid is to be prepared; where Z is an electron-withdrawing group; wherein Y is a leaving group for nucleophilic substitution; wherein R 3 corresponds to one or more suitable protecting groups for an amino function; wherein R 4 corresponds to a suitable protecting group for a carboxyl function; (2) nucleophilic substitution of Y by a negatively charged [ 18 F] fluoride ion to prepare the compound shown below: (3) Cleavage of Z to produce the compound shown below: (4) hydrolytic cleavage of R 3 and R 4 for the preparation of the compound shown below: (5) hydrolytic cleavage of R 1 and R 2 for the preparation of the [ 18 F] fluorine-labeled aromatic L-amino acid shown below: wherein R 5 and R 6 are substituents each corresponding to an H atom or an OH group.
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