Methods for carbon isotope labeling synthesis by transition metal-promoted carbonylation via isocyanate using azides and carbon-isotope monoxide
Methods and reagents for transition metal-promoted carbonylation via isocyanate using carbon-isotope labeled carbon monoxide are provided. The resultant carbon-isotope labeled compounds are useful as radiopharmaceuticals, especially for use in Positron Emission Tomography (PET). Associated kits for PET studies are also provided.
1. A method of using produced carbon-isotope enriched gas mixture in labeling synthesis, comprising:
(a) providing a high pressure reaction chamber having a liquid inlet and a gas inlet in a bottom surface thereof,
(b) providing an azide solution to be labeled comprising an azide of the formula R 1 —N 3 , wherein R 1 , is linear or cyclic lower alkyl or substituted alkyl, hydrogen, aryl or substituted aryl and optionally comprises carbonyl, hydroxy, thiol, halogen, nitrile, isonitrile, cyanate, isocyanate, thiocyanate, isothiocyanate functional groups,
a transitional metal complex and a reagent,
wherein the reagent is:
R 2 , R 3 , R 4 , and R 5 are independently linear or cyclic lower alkyl or substituted alkyl, hydrogen, aryl, or substituted aryl, and optionally comprise carbonyl, hydroxy, thiol, halogen, nitrile, isonitrile, cyanate, isocyanate, thiocyanate, isothiocyanate functional groups,
(c) introducing a carbon-isotope monoxide enriched gas-mixture into the reaction chamber via the gas inlet,
(d) introducing, at high pressure, said azide solution comprising said transition metal complex and one of said reagents into the reaction chamber via the liquid inlet,
(e) waiting for a predetermined time while said labeling synthesis occurs, and
(f) collecting the labeled compound from the reaction chamber, wherein the labeled compound is:
wherein R 1 , is linear or cyclic lower alkyl or substituted alkyl, hydrogen, aryl or substituted aryl and optionally comprises carbonyl, hydroxy, thiol, halogen, nitrile, isonitrile, cyanate, isocyanate, thiocyanate, isothiocyanate functional groups and R 2 , R 3 , R 4 and R 5 are independently linear or cyclic lower alkyl or substituted alkyl, hydrogen, aryl or substituted aryl, and optionally comprise carbonyl, hydroxy, thiol, halogen, nitrile, isonitrile, cyanate, isocyanate, thiocyanate, isothiocyanate functional groups, and * is the labeled carbon position.
2. A method of claim 1 , wherein the carbon-isotope monoxide enriched gas-mixture is produced by a method comprising:
(a) providing carbon-isotope dioxide in a suitable carrier gas,
(b) converting carbon-isotope dioxide to carbon-isotope monoxide by introducing said gas mixture in a reactor device,
(c) trapping carbon-isotope monoxide in a carbon monoxide trapping device, wherein carbon-isotope monoxide is trapped but not said carrier gas, and
(d) releasing said trapped carbon-isotope monoxide from said trapping device in a well defined micro-plug, whereby a volume of carbon-isotope monoxide enriched gas-mixture is achieved.
3. A method of claim 1 , wherein the carbon-isotope is 11 C, 13 C, or 14 C.
4. A method of claim 1 , wherein the carbon-isotope is 11 C.
5. A method of claim 1 , wherein the step of introducing the azide solution to be labeled mixed with a transitional metal complex and an appropriate other reagent is performed using a pressure that is about 80 times higher than the pressure before the introduction, in order to maintain a pseudo one-phase system.
6. A method of claim 1 , wherein the step of waiting a predetermined time comprises adjusting the temperature of the reaction chamber to enhance the labeling synthesis.
7. A method of claim 1 , wherein the transitional metal complex is a rhodium complex.
8. A method of claim 1 , furthering comprising deprotection to give the labeled compound and respective addition of one of said reagents.
9. A method of using produced carbon-isotope enriched gas mixture in labeling synthesis, comprising:
(a) providing a high pressure reaction chamber having a liquid inlet and a gas inlet in a bottom surface thereof,
(b) providing an azide solution to be labeled comprising an azide of the formula:
and a transitional metal complex,
(c) introducing a carbon-isotope monoxide enriched gas-mixture into the reaction chamber via the gas inlet,
(d) introducing, at high pressure, said azide solution comprising said transition metal complex into the reaction chamber via the liquid inlet,
(e) waiting for a predetermined time while said labeling synthesis occurs, and
(f) collecting the labeled compound from the reaction chamber, wherein the labeled compound is:
and * is the labeled carbon position.