Two routes to [11C-carbonyl]organo-isocyanates utilizing [11C]phosgene ([11C]organo-isocyanates from [11C]phosgene)
Brown, Gavin D.; Henderson, David; Steel, Colin; Luthra, Sajinder; Price, Patricia M.; Brady, Frank, E-mail: gavin.brown@ic.ac.uk2001
AbstractAbstract
[en] Two generic radiosynthetic routes for the preparation of [11C-carbonyl]isocyanates have been developed. Reaction of N-organo-sulfinylamines; RNSO, (R=Me, Et, allyl, cyclohexyl and phenyl) with [11C]phosgene gave the corresponding [11C-carbonyl]isocyanates in good radiochemical yield (53-68%) from [11C]phosgene (decay corrected) in ca 16 min from EOB. Alternatively, the reaction of [11C]phosgene with N,N'-organo-ureas; (RNH)2CO, (R=Me, Et, Pr and phenyl) also gave the corresponding [11C-carbonyl]isocyanates in moderate radiochemical yield (9-37%) from [11C]phosgene (decay corrected) in ca 16 min from EOB. For identification, the [11C-carbonyl]organo-isocyanates were derivatized with 1-(2-methoxyphenyl)piperazine in situ to [11C-carbonyl]carboxamides and the position of radiolabelling in the carbonyl group confirmed by [11/13C]co-labeling and subsequent carbon-13 NMR spectroscopy
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S0969805101002633; Copyright (c) 2001 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: Estonia
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Descriptors (DEC)
BETA DECAY RADIOISOTOPES, BETA-PLUS DECAY RADIOISOTOPES, CARBON ISOTOPES, CARBONIC ACID DERIVATIVES, EVEN-ODD NUCLEI, ISOTOPES, LIGHT NUCLEI, MINUTES LIVING RADIOISOTOPES, NITROGEN COMPOUNDS, NUCLEI, ORGANIC CHLORINE COMPOUNDS, ORGANIC COMPOUNDS, ORGANIC HALOGEN COMPOUNDS, RADIOISOTOPES, STABLE ISOTOPES, SYNTHESIS
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