methyl 5-[2-(2-amino-4-methoxyphenyl)-1,3-dithian-2-yl]pentanoate | 1415336-56-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: methyl 5-[2-(2-amino-4-methoxyphenyl)-1,3-dithian-2-yl]pentanoate
• 英文别名: Methyl 5-(2-(2-amino-4-methoxyphenyl)-1,3-dithian-2-yl)pentanoate
• CAS: 1415336-56-9
• 化学式: C₁₇H₂₅NO₃S₂
• 分子量: 355.522
• InChiKey: HYWSXNVNCPJQAK-UHFFFAOYSA-N

物化性质

• 沸点：
  506.5±50.0 °C(predicted)
• 密度：
  1.179±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  23
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  112
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  methyl 5-[2-(2-amino-4-methoxyphenyl)-1,3-dithian-2-yl]pentanoate 在 哌啶 、 碳酸氢钠 、 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 反应 22.0h， 生成 (R)-methyl 5-(2-{2-[2-(2-{[(tert-butoxy)carbonyl]amino}acetamido)propanamido]-4-methoxyphenyl}-1,3-dithian-2-yl)pentanoate
  参考文献：
  名称：

  Studies toward the Synthesis of Potent Anti-inflammatory Peptides Solomonamides A and B: Synthesis of a Macrocyclic Skeleton and Key Fragment 4-Amino-6-(2′-amino-4′-hydroxyphenyl)-3-hydroxy-2-methyl-6-oxohexanoic Acid (AHMOA)

  摘要：

  A first synthetic effort toward total synthesis of highly potent solomonamides is disclosed. An efficient strategy to synthesize this class of compounds, along with the synthesis of a core macrocycle (shown in red) and the key fragment AHMOA, is described.

  DOI：

  10.1021/ol303149k
• 作为产物：
  描述：

  6-氧代己酸甲酯 在 盐酸 、 palladium(II) trifluoroacetate 、 三氟化硼乙醚 作用下， 以 二氯甲烷 、 水 、 甲苯 为溶剂， 反应 44.0h， 生成 methyl 5-[2-(2-amino-4-methoxyphenyl)-1,3-dithian-2-yl]pentanoate
  参考文献：
  名称：

  Studies toward the Synthesis of Potent Anti-inflammatory Peptides Solomonamides A and B: Synthesis of a Macrocyclic Skeleton and Key Fragment 4-Amino-6-(2′-amino-4′-hydroxyphenyl)-3-hydroxy-2-methyl-6-oxohexanoic Acid (AHMOA)

  摘要：

  A first synthetic effort toward total synthesis of highly potent solomonamides is disclosed. An efficient strategy to synthesize this class of compounds, along with the synthesis of a core macrocycle (shown in red) and the key fragment AHMOA, is described.

  DOI：

  10.1021/ol303149k

文献信息

• SOLOMONAMIDE ANALOGUE COMPOUNDS, PHARMACEUTICALS CONTAINING SOLOMONAMIDE ANALOGUE COMPOUNDS, AND PROCESSES FOR THE PREPARATION THEREOF
  申请人：COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH

  公开号：US20150291659A1

  公开（公告）日：2015-10-15

  Solomanamide analogues of Formula-I having anti-inflammatory activity, and viable synthetic routes for the preparation of such analogues, including the synthesis of macrocyclic core of Salomanamide analogues. The Solomanamide analogues of Formula-I or their pharmaceutical salt may be provided in a pharmaceutical composition and administered in an effective amount for the treatment of inflammation and/or pain.

  公式I的Solomanamide类似物具有抗炎活性，并且具有制备这种类似物的可行合成路线，包括制备Salomanamide类似物的大环核心的合成。公式I的Solomanamide类似物或其药物盐可以在药物组合物中提供，并以有效剂量用于治疗炎症和/或疼痛。
• A PROCESS FOR THE PREPARATION OF SOLOMONAMIDE ANALOGUES
  申请人：Council of Scientific & Industrial Research

  公开号：EP2925771A1

  公开（公告）日：2015-10-07
• US9751911B2
  申请人：——

  公开号：US9751911B2

  公开（公告）日：2017-09-05
• [EN] A PROCESS FOR THE PREPARATION OF SOLOMONAMIDE ANALOGUES<br/>[FR] PROCÉDÉ DE PRÉPARATION D'ANALOGUES DU SOLOMONAMIDE
  申请人：COUNCIL OF SCIENT & IND RESERACH AN INDIAN REGISTERED BODY INC UNDER THE REGN OF SOC ACT ACT XXI OF

  公开号：WO2014083578A1

  公开（公告）日：2014-06-05

  The invention disclosed herein relates to novel solomonamide analogues of formula I having anti-inflammatory activity and viable synthetic route for the preparation thereof.
• Studies toward the Synthesis of Potent Anti-inflammatory Peptides Solomonamides A and B: Synthesis of a Macrocyclic Skeleton and Key Fragment 4-Amino-6-(2′-amino-4′-hydroxyphenyl)-3-hydroxy-2-methyl-6-oxohexanoic Acid (AHMOA)
  作者：K. Kashinath、N. Vasudevan、D. Srinivasa Reddy

  DOI：10.1021/ol303149k

  日期：2012.12.21

  A first synthetic effort toward total synthesis of highly potent solomonamides is disclosed. An efficient strategy to synthesize this class of compounds, along with the synthesis of a core macrocycle (shown in red) and the key fragment AHMOA, is described.