tert-butyl (2S,3R)-3-[tert-butyl(dimethyl)silyl]oxy-5-[(4-methylphenyl)sulfonylamino]-2-thiophen-2-yl-2,4-dihydropyrrole-3-carboxylate | 1298087-80-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: tert-butyl (2S,3R)-3-[tert-butyl(dimethyl)silyl]oxy-5-[(4-methylphenyl)sulfonylamino]-2-thiophen-2-yl-2,4-dihydropyrrole-3-carboxylate
• CAS: 1298087-80-5
• 化学式: C₂₆H₃₈N₂O₅S₂Si
• 分子量: 550.816
• InChiKey: KEBPCELCSXVVGU-ATIYNZHBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.98
• 重原子数：
  36
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  131
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  对甲苯磺酰胺 在 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 、 乙基苯 为溶剂， 反应 17.5h， 生成 tert-butyl (2S,3R)-3-[tert-butyl(dimethyl)silyl]oxy-5-[(4-methylphenyl)sulfonylamino]-2-thiophen-2-yl-2,4-dihydropyrrole-3-carboxylate
  参考文献：
  名称：

  Three-Component Reactions of Sulfonylimidates, Silyl Glyoxylates and N-tert-Butanesulfinyl Aldimines: An Efficient, Diastereoselective, and Enantioselective Synthesis of Cyclic N-Sulfonylamidines

  摘要：

  Three-component coupling reactions of sulfonylimidates, silyl glyoxylates and N-tert-butanesulfinyl aldimines efficiently provide cyclic N-sulfonylamiclines containing free endocyclic N-H. The formation of two C-C bonds (contiguous stereogenic carbons), one O-Si bond, and one C-N bond, together with the cleavage of the chiral auxiliary (tert-butanesulfinyl group), occurs with excellent chemoselectivity, diastereoselectivity, and enantioselectivity in this one-pot cascade transformation.

  DOI：

  10.1021/ol201029b

文献信息

• Three-Component Reactions of Sulfonylimidates, Silyl Glyoxylates and <i>N</i>-<i>tert</i>-Butanesulfinyl Aldimines: An Efficient, Diastereoselective, and Enantioselective Synthesis of Cyclic <i>N</i>-Sulfonylamidines
  作者：Ming Yao、Chong-Dao Lu

  DOI：10.1021/ol201029b

  日期：2011.5.20

  Three-component coupling reactions of sulfonylimidates, silyl glyoxylates and N-tert-butanesulfinyl aldimines efficiently provide cyclic N-sulfonylamiclines containing free endocyclic N-H. The formation of two C-C bonds (contiguous stereogenic carbons), one O-Si bond, and one C-N bond, together with the cleavage of the chiral auxiliary (tert-butanesulfinyl group), occurs with excellent chemoselectivity, diastereoselectivity, and enantioselectivity in this one-pot cascade transformation.