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1.
J Labelled Comp Radiopharm ; 60(4): 194-199, 2017 04.
Artículo en Inglés | MEDLINE | ID: mdl-28129428

RESUMEN

MK 3814 is a potent and selective antagonist of the A2a receptor. A2a receptor antagonists have the potential for the treatment of Parkinson disease. Three distinct isotopically labelled forms of MK 3814 were synthesized. [3 H]MK 3814 was prepared for a preliminary absorption, distribution, metabolism, and excretion data (ADME) evaluation of the compound and [14 C]MK 3814 for more definitive ADME work, including an absorption, metabolism, and excretion study in man. In addition, [2 H4 ]MK 3814 was prepared as an internal standard for a liquid chromatography mass spectrometry bioanalytical method. This paper discusses the synthesis of 3 isotopically labelled forms of MK 3814.


Asunto(s)
Radioisótopos de Carbono/química , Deuterio/química , Pirimidinas/química , Pirimidinas/síntesis química , Triazoles/química , Triazoles/síntesis química , Tritio/química , Técnicas de Química Sintética , Marcaje Isotópico
2.
J Labelled Comp Radiopharm ; 58(2): 36-41, 2015 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-25689968

RESUMEN

The synthesis of [(3)H]SCH 466036, [Me-(3)H3]SCH 466036, [(13)C,(2)H3,(15)N]SCH 466036 and [(14)C]SCH 466036 is described. [(3)H]SCH 466036 was prepared in two steps via Raney Ni-catalysed exchange with tritiated water. [Me-(3)H3]SCH 466036 was prepared in a single step from [(3)H]methyl iodide in 45% yield. [(13)C,(2)H3,(15)N]SCH 466036 was prepared in two steps from [(15)N]hydroxylamine and [(13)C,(2)H3]methyl iodide with an overall yield of 16%. [(14)C]SCH 466036 was prepared in seven steps from [(14)C]potassium cyanide in an overall yield of 13%.


Asunto(s)
Aminopiridinas/síntesis química , Antagonistas de los Receptores Histamínicos H3/síntesis química , Piperidinas/síntesis química , Radiofármacos/síntesis química , Aminopiridinas/farmacología , Radioisótopos de Carbono/química , Deuterio/química , Isótopos de Nitrógeno/química , Piperidinas/farmacología , Tritio/química
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