http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02102765-A3

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filingDate 2002-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb7976b127db9c39bd427eab010ddd6b
publicationDate 2003-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-02102765-A3
titleOfInvention Protected tyrosine derivatives, method for the production thereof and use of the same for producing o-(2-[18f]-fluoroethyl)-l-tyrosine
abstract The compound O-(2-[18F]fluoroethyl)-L-tyrosine has proven to be particularly suitable for positron emission tomography and has already been tested in clinical practice. Until now, the compound has been produced according to a relatively laborious method (Wester H.J. et al.; J. Nucl. Med. 1999; 40: 205-212). The invention relates to L-tyrosine derivatives of formula (1), wherein R1 represents a suitable protective group for the carboxy group, R2 represents a suitable protective group for the amino group, and R3 represents a suitable leaving group. R1 represents a methylthiomethyl group, a tetrahydrofuranyl group, a diphenylmethyl group, a para-methoxybenzyl group, a piperonyl group or a tert-butyl group, R2 represents an alkyl group or an arylalkyl group, and R3 represents a p-tosyloxy, methanesulfonyloxy, trifluoromethanesulfonyloxy or bromine. The invention also relates to a method for producing O-(2-[18F]-fluoroethyl)-L-tyrosine from the parent compounds of formula (1) and to a method for producing said parent compounds.
priorityDate 2001-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 36.