3-benzyl-thiazolidine | 67824-24-2

• 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: 3-benzyl-thiazolidine
• 英文别名: n-Benzylthiazolidine；3-benzyl-1,3-thiazolidine
• CAS: 67824-24-2
• 化学式: C₁₀H₁₃NS
• 分子量: 179.286
• InChiKey: NPJVMONBELCBQG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  28.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  3-benzylthiazolidin-2-ylidenecyanamide 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 以60%的产率得到3-benzyl-thiazolidine
  参考文献：
  名称：

  Regioslective Hydride Reduction of 2-(N-cyanoimino)thiazolidine Derivatives

  摘要：

  Treatment of 3-alkyl-2-(N-cyanoimino)thiazolidines with lithium aluminum hydride caused reductive cleavage of the imino double bond to afford 3-alkylthiazolidines, while diisobutylaluminum hydride reduction of 3-alkyl- and 3-sulfonyl derivatives resulted in the nitrile reduction or imino-nitrile bond cleavage to give 2-formyliminothiazolidines and/or 2-iminothiazolidines.

  DOI：

  10.3987/com-91-5896

文献信息

• PROCESS FOR PRODUCING COMPOUND WITH ANTI-HCV POTENCY AND INTERMEDIATE FOR USE THEREIN
  申请人：CHUGAI SEIYAKU KABUSHIKI KAISHA

  公开号：EP1857456A1

  公开（公告）日：2007-11-21

  A method whereby a compound having HCV replication inhibitory activity and desired optical activity can be synthesized selectively and at high yield in a small number of steps by using a compound having a specific chiral auxiliary as a starting compound is provided. A compound represented by the formula (1-8): [wherein Y represents a group represented by the following formula: Q represents a protected carbonyl group; D represents -(CH2)m-R', etc.; and n represents an integer of 0 to 10].

  本发明提供了一种方法，通过使用具有特定手性助剂的化合物作为起始化合物，可以在少量步骤内选择性地高产率合成具有 HCV 复制抑制活性和所需光学活性的化合物。 由式（1-8）代表的化合物： [其中 Y 代表下式所表示的基团： Q 代表受保护的羰基；D 代表-(CH2)m-R'等；n 代表 0 至 10 的整数]。
• Kametani,T. et al., Heterocycles, 1978, vol. 9, p. 831 - 840
  作者：Kametani,T. et al.

  DOI：——

  日期：——
• KAMETANI T.; KIGASAWA K.; HIIRAGI M.; WAGATSUMA N.; KOHAGIZAWA T.; INOUE +, HETEROCYCLES, 1978, 9, NO 7, 831-840
  作者：KAMETANI T.、 KIGASAWA K.、 HIIRAGI M.、 WAGATSUMA N.、 KOHAGIZAWA T.、 INOUE +

  DOI：——

  日期：——
• Production Process of Compound Having Anti-Hcv Action and Intermediate Thereof
  申请人：Kato Tatsuya

  公开号：US20080293950A1

  公开（公告）日：2008-11-27

  A method whereby a compound having HCV replication inhibitory activity and desired optical activity can be synthesized selectively and at high yield in a small number of steps by using a compound having a specific chiral auxiliary as a starting compound is provided. A compound represented by the formula (1-8): [wherein Y represents a group represented by the following formula: Q represents a protected carbonyl group; D represents —(CH 2 ) m —R′, etc.; and n represents an integer of 0 to 10].
• Intermediate compound for synthesis of viridiofungin a derivative
  申请人：Kato Tatsuya

  公开号：US20100152456A1

  公开（公告）日：2010-06-17

  A method whereby a compound having HCV replication inhibitory activity and desired optical activity can be synthesized selectively and at high yield in a small number of steps by using a compound having a specific chiral auxiliary as a starting compound is provided. A compound represented by the formula (1-8): wherein Y represents a group represented by the following formula: Q represents a protected carbonyl group; D represents —(CH 2 ) m —R′, etc.; and n represents an integer of 0 to 10.