5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-L-sorbopyranose | 927809-72-1

• 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: 5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-L-sorbopyranose
• CAS: 927809-72-1
• 化学式: C₂₃H₂₅N₃O₆
• 分子量: 439.468
• InChiKey: MPQANORBJUSHDW-SRYPRDQNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.99
• 重原子数：
  32.0
• 可旋转键数：
  6.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  111.98
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-L-sorbopyranose 在 镍 咪唑 、 氢气 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三氟乙酸 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 20.0 ℃ 、413.68 kPa 条件下， 反应 122.5h， 生成 (2S,3R,4R,5R)-2'-O-benzoyl-N-benzyl-4-benzyloxy-5'-O-tert-butyldiphenylsilyl-3-hydroxy-2,5-bis(hydroxymethyl)-pyrrolidine
  参考文献：
  名称：

  Polyhydroxylated pyrrolidines: synthesis from d-fructose of new tri-orthogonally protected 2,5-dideoxy-2,5-iminohexitols

  摘要：

  The readily available 3-O-benzyl-1,2-O-isopropylidene-beta-D-fructopyranosc (2) was transformed into its 5-O-(3) and 4-O-benzoyl (4) derivative. Compound 4 was straightforwardly transformed into 5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-beta D-fructopyranose (7) via the corresponding 5-deoxy-5-iodo-alpha-L-sorbopyranose derivative 6. Cleavage of the acetonide in 7 to give 8, followed by regioselective 1-O-silylation to 9 and subsequent catalytic hydrogenation gave a mixture of (2S,3R,4R,5R)-(10) and (2R,3R,4R,5R)-4-benzoyloxy-3-benzyloxy-2'-O-tert-butyldiphenylsilyl-2,5-bis(hydroxymethyl)pyrrolidine (12) that was resolved after chemoselective N-protection as their Cbz derivatives 11 and la, respectively. Stereochemistry of 11 and la could be determined after total deprotection of 11 to the well known DGDP (13). Compound 2 was similarly transformed into the tri-orthogonally protected DGDP derivative 18. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2006.11.070
• 作为产物：
  描述：

  10-(benzyloxy)-2,2-dimethyl-1,3,6-trioxaspiro(4,5)decane-8,9-diol 在 吡啶 、 偶氮二甲酸二异丙酯 、 二苯基磷酸 、 三苯基膦 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-L-sorbopyranose
  参考文献：
  名称：

  Polyhydroxylated pyrrolidines: synthesis from d-fructose of new tri-orthogonally protected 2,5-dideoxy-2,5-iminohexitols

  摘要：

  The readily available 3-O-benzyl-1,2-O-isopropylidene-beta-D-fructopyranosc (2) was transformed into its 5-O-(3) and 4-O-benzoyl (4) derivative. Compound 4 was straightforwardly transformed into 5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-beta D-fructopyranose (7) via the corresponding 5-deoxy-5-iodo-alpha-L-sorbopyranose derivative 6. Cleavage of the acetonide in 7 to give 8, followed by regioselective 1-O-silylation to 9 and subsequent catalytic hydrogenation gave a mixture of (2S,3R,4R,5R)-(10) and (2R,3R,4R,5R)-4-benzoyloxy-3-benzyloxy-2'-O-tert-butyldiphenylsilyl-2,5-bis(hydroxymethyl)pyrrolidine (12) that was resolved after chemoselective N-protection as their Cbz derivatives 11 and la, respectively. Stereochemistry of 11 and la could be determined after total deprotection of 11 to the well known DGDP (13). Compound 2 was similarly transformed into the tri-orthogonally protected DGDP derivative 18. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2006.11.070