2-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-1,3-thiazole | 154127-57-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-1,3-thiazole
• 英文别名: 2-(2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl)thiazole；2-((3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-2-(thiazol-2-yl)-tetrahydro-2H-pyran-2-yl)thiazole；2-[(2S,3R,4S,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]-1,3-thiazole
• CAS: 154127-57-8
• 化学式: C₃₇H₃₇NO₅S
• 分子量: 607.77
• InChiKey: QBHWFPXQVMFWJI-GJXDWMKPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.1
• 重原子数：
  44
• 可旋转键数：
  14
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  87.3
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  2-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-1,3-thiazole 在 sodium methylate 作用下， 反应 24.0h， 生成 2-(2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl)thiazole 、 1-C-thiazolyl-3,4,6-tri-O-benzyl-D-glucal
  参考文献：
  名称：

  以苯并噻唑为甲酰基当量的甲级四-O-苄基-β-d- C-吡喃葡萄糖苷的数克级合成

  摘要：

  向d-葡糖酸内酯中加入2-硫代苯并噻唑，然后将所得酮糖脱氧，得到苯并噻唑基α-和β-d-吡喃葡萄糖苷的混合物。用甲醇钠处理该混合物得到β-异头物，通过将苯并噻唑环转化成甲酰基，以纯净形式得到标题醛。

  DOI：

  10.1016/s0040-4039(02)02525-x
• 作为产物：
  描述：

  2,3,4,6-四苄基-D-吡喃葡萄糖 在 三乙基硅烷 、 正丁基锂 、 三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 、 pyridinium chlorochromate 作用下， 以 二氯甲烷 为溶剂， 反应 2.33h， 生成 2-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-1,3-thiazole
  参考文献：
  名称：

  Thiazole-Based Synthesis of Formyl C-Glycosides

  摘要：

  A method for the installation of the formyl group at the anomeric position of pyranoses and furanoses starting from the corresponding lactones has been developed. The strategy involves the addition of 2-lithiothiazole to the sugar lactone, followed by the silane reduction of the acetylated resultant ketol and the unmasking of the formyl group from the thiazole ring. All steps have been studied in some details to improve chemical efficiency and stereochemical control. Hence, reversed alpha:beta ratios of ketols were found in kinetic and thermodynamic mixtures, the former being consistent with a steric effect control of the substituents and the latter by the electronic effect of the ring oxygen. Seven sugar aldehydes with different D-pyranosidic (2,3,4,6-tetra-O-benzyl-gluco, -galacto, and -manno, 2-azido-3,4,6-tri-O-benzyl-2-deoxy-galacto) and D-furanosidic moieties (5-O-benzyl-2,3-isopropylidene-ribo; 2,3,5-tri-O-benzyl-ribo; 2,3:5,6-di-O-isopropylidene-manno) were prepared in 52-65% isolated overall yield from the corresponding lactone.

  DOI：

  10.1021/jo00100a050

文献信息

• Selectivity in the SmI2-induced deoxygenation of thiazolylketoses for formyl C-glycoside synthesis and revised structure of C-ribofuranosides
  作者：Alessandro Dondoni、Paolo Formaglio、Alberto Marra、Alessandro Massi

  DOI：10.1016/s0040-4020(01)00736-0

  日期：2001.9

  Deoxygenation of thiazolylketose acetates using SmI2–(CH2OH)2 or TMSOTf–Et3SiH affords thiazolyl C-glycosides with opposite α/β ratios. Examination of the thiazolyl α- and β-C-ribofuranoside pair by NOE experiments reveals that the earlier configuration assigned to one of these isomers has to be revised. Having prepared authentic anomeric α- and β-ribofuranose aldehydes from the corresponding thiazolyl

  使用SmI 2-（CH 2 OH）2或TMSOTf-Et 3 SiH对乙酸噻唑基酮糖乙酸进行脱氧，得到具有相反α/β比的噻唑基C-糖苷。通过NOE实验对噻唑基α-和β- C-核呋喃糖苷对的研究表明，必须修改分配给这些异构体之一的早期构型。已经制备正品异头α-和β-D-呋喃核糖醛从相应的噻唑基C ^由噻唑环的裂解-glycosides，各醛转化到（1→6） - c ^通过Wittig烯化-disaccharides与半乳糖6-正膦。
• Synthesis of pyridazine and thiazole analogs as SGLT2 inhibitors
  作者：Suk Youn Kang、Kwang-Seop Song、Junwon Lee、Sung-Han Lee、Jinhwa Lee

  DOI：10.1016/j.bmc.2010.06.076

  日期：2010.8

  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.
• Thiazole-based synthesis of C-glycosyl aldehydes
  作者：Alessandro Dondoni、Marie-Christine Scherrmann

  DOI：10.1016/s0040-4039(00)79319-1

  日期：1993.11

  The formylation at the anomeric carbon of the model sugars 2,3,4,6-tetra-O-benzyl-D-glucopyranose and 2,3:5,6-di-O-isopropylidene-D-mannofuranose is carried out by addition of 2-lithiothiazole to the corresponding lactones followed by reductive dehydroxylation and thiazole to formyl deblocking.