4-((triisopropylsilyloxy)methyl)-2-((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)thiazole | 1242653-98-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-((triisopropylsilyloxy)methyl)-2-((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)thiazole
• CAS: 1242653-98-0
• 化学式: C₄₇H₅₉NO₆SSi
• 分子量: 794.14
• InChiKey: KIBSVYAECMVKIT-FNGPDGFESA-N

反应信息

• 作为反应物：
  描述：

  4-((triisopropylsilyloxy)methyl)-2-((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)thiazole 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 生成 (2-((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)thiazol-4-yl)methanol 、 (2-((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)thiazol-4-yl)methanol
  参考文献：
  名称：

  Synthesis of pyridazine and thiazole analogs as SGLT2 inhibitors

  摘要：

  With anticipation of the improvement in biological aspects in our SGLT2 program, novel pyridazinyl and thiazolyl analogs were designed and efficiently synthesized. The installation of the pyridazine ring at the anomeric carbon of D-glucopyranose was carried out in a stereoselective fashion. On the other hand, a series of thiazolyl analogs was also synthesized through a coupling reaction between perbenzyl gluconolactone 9 and 2-lithiothiazole. Biological activities of the compounds thus prepared were evaluated by the in vitro SGLT2 inhibition assay. Considering assay results, the novel benzylpyridazinyl and benzyl-thiazolyl analogs, disclosed in this article, could be a quick reference to prospective SGLT2 inhibitors useful for pharmacotherapy. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.06.076