Kumamoto Hiroki, Onuma Sayoko, Tanaka Hiromichi
School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
J Org Chem. 2004 Jan 9;69(1):72-8. doi: 10.1021/jo030256y.
A new approach has been developed for the synthesis of potential inhibitors of S-adenosyl-l-homocysteine (AdoHcy) hydrolase. The key intermediate 9-[2,3-bis-O-(tert-butyldimethylsilyl)-5-(Z)-(tributylstannyl)-5-deoxy-beta-d-erythro-pent-4-enofuranosyl]adenine (12) was prepared by sulfur extrusion reaction of 4',5'-didehydro-5'-deoxy-5'-(phenylthio)adenosine (11) with tributyltin radical. It was found that this reaction proceeds stereoselectively, forming 12 irrespective of the geometry of 11. Compound 12 readily underwent iodination, bromination, and chlorination with retention of configuration, whereas fluorination gave both (Z)- and (E)-isomers of vinyl fluoride. Because of the susceptibility of 12 to protodestannylation, the (Z)-vinyl iodide (13), prepared in quantitative yield from 12, was used as a substrate for C-C bond formation. Various types of carbon substituents (phenyl, vinyl, trifluorovinyl, ethynyl, and cyano) were introduced to the 5'-position of the 5-deoxy-beta-d-erythro-pent-4-enofuranosyl structure to open up a new route to potential inhibitors of AdoHcy hydrolase.
一种用于合成S-腺苷-L-高半胱氨酸(AdoHcy)水解酶潜在抑制剂的新方法已经开发出来。关键中间体9-[2,3-双-O-(叔丁基二甲基甲硅烷基)-5-(Z)-(三丁基锡烷基)-5-脱氧-β-D-赤式-戊-4-烯呋喃糖基]腺嘌呤(12)是通过4',5'-二脱氢-5'-脱氧-5'-(苯硫基)腺苷(11)与三丁基锡自由基的脱硫反应制备的。发现该反应具有立体选择性,无论11的几何构型如何都能形成12。化合物12容易进行碘化、溴化和氯化反应且构型保持不变,而氟化反应则生成了乙烯基氟的(Z)-和(E)-异构体。由于12对原脱锡反应敏感,由12定量制备的(Z)-乙烯基碘(13)被用作形成C-C键的底物。将各种类型的碳取代基(苯基、乙烯基、三氟乙烯基、乙炔基和氰基)引入到5-脱氧-β-D-赤式-戊-4-烯呋喃糖基结构的5'-位,以开辟一条通往AdoHcy水解酶潜在抑制剂的新途径。