- Challenges and difficulties in synthesis of tritium labeled fluocinolone acetonide
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Tritium labeled fluocinolone acetonide was synthesized through five-step procedure. Many challenges and difficulties were encountered in the synthesis, especially in the regeneration of 1,2 double bond from reaction of oxidative de-hydrogenation of tritium labeled 4-ene analog. Selenium oxide oxidative de-hydrogenation of 11,21-dihydroxy un-protected 4-ene fluocinolone acetonide analog gave a complex product mixture. The reaction gave a clean unlabeled intermediate after protection of 21-hydroxy group by acetylation, but the same procedure failed to give desired tritium labeled intermediate due to fast tritium-hydrogen exchange reaction. The de-hydrogenation proceeded well with DDQ in refluxing benzene for unlabeled intermediate, but no reaction at all for the tritium labeled one. Benzeneseleninic anhydride/toluene refluxed with tritium labeled 4-ene analog was found to be the best de-hydrogenation reaction conditions after exploring suitable conditions. Detailed examination of the de-hydrogenation product, 1,4-diene analog by radio-HPLC, HPLC-MS, proton and tritium NMR found that not only had the de-hydrogenation taken place, but also 11-hydroxy group was oxidized to ketone at the same time. This problem was resolved by acetylation protection of both 11,21-dihydoxy groups. De-protection of tritium labeled 11,21-diacetyl 1,4-diene intermediate in K2CO 3/CH3OH/H2O gave expected final product, [1,2-3H]fluocinolone acetonide with a specific activity of 36.8 Ci/mmol (radiochemical purity: 97%) after purification. Copyright
- Zhong, Desong,Lewin, Anita H.
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p. 260 - 265
(2011/05/06)
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- Preparation of high specific activity tritium labeled 6α,9,-difluoro- 11 β,21-dihydroxy- 16α,17-[(1-methylethylidene)bis(oxy)]pregna- 1,4-diene-3,20-one, fluocinolone acetonide
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Fluocinolone acetonide was tritiated by selective reduction of the 1,2-double bond of the O-protected analog under tritium, followed by re-establishment of the 1,2-double bond and deprotection. Protection of both hydroxyl functionalities was required. The product was obtained with specific activity 36.8Ci/mmol. Copyright
- Zhong,Lewin, Anita H.
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p. 103 - 109
(2009/10/24)
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