Långström B, Antoni G, Gullberg P, Halldin C, Malmborg P, Någren K, Rimland A, Svärd H
J Nucl Med. 1987 Jun;28(6):1037-40.
This report describes the synthesis of L- and D-[methyl-11C]methionine in pure enantiomeric forms. The compounds were prepared routinely approximately 1,000 times with less than 20 failures. Starting with carbon-11 (11C) methyl iodide, a simple one-carbon precursor produced from a one-pot or a two-pot apparatus, L- and D-[methyl-11C]methionine were prepared, respectively, with an optical purity higher than 99% in 40%-90% radiochemical yields. The total time for synthesis, starting from [11C]carbon dioxide, was 12-15 min. The crude product usually had a radiochemical purity greater than 95%. The total time for synthesis, including LC purification, was 20-30 min. The radiochemical purity of the product in each case was greater than 98%.
本报告描述了纯对映体形式的L-和D-[甲基-¹¹C]蛋氨酸的合成。这些化合物常规制备了约1000次,失败次数少于20次。以¹¹C甲基碘为起始原料,通过一锅法或两锅法装置制备的一种简单的一碳前体,分别制备出光学纯度高于99%、放射化学产率为40%-90%的L-和D-[甲基-¹¹C]蛋氨酸。从¹¹C二氧化碳开始合成的总时间为12-15分钟。粗产物的放射化学纯度通常大于95%。包括液相色谱纯化在内的合成总时间为20-30分钟。每种情况下产物的放射化学纯度均大于98%。