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filingDate 2005-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b98807cab9e0ca539c290cad826ccda
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publicationDate 2006-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7138540-B1
titleOfInvention Convenient method for the preparation of new precursor of no-carrier-added O-(2-[18F]fluoroethyl)-L-Tyrosine)
abstract This is a new precursor and new method for the synthesis of no-carrier-added O-(2-[ 18 F]fluoroethyl)-L-Tyrosine which has been proved a suitable PET (position emission tomography) probe for tumor diagnosis imaging, the preparation of the title compound starts from precursors with the chemical structures as in Formula 1, wherein R 1 is a protective group for the carboxyl functional group, R 2 is a protective group for the amino group, and R 3 acts as a leaving group. R 1 represents an arylalkyl group, R 2 represents a carboxyl group, and R 3 represents a p-tosyloxy, methane sulfonyloxy or trifluoromethane sulfonyloxy or bromine, the invention includes a method for the syntheses of new precursors with the chemical structures as in Formula 1.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3231804-A1
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