3-(2,3-dihydro-1,4-benzodioxin-5-yl)propionic acid | 214895-00-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并二恶烷
• 英文名称: 3-(2,3-dihydro-1,4-benzodioxin-5-yl)propionic acid
• 英文别名: 3-(2,3-dihydro-benzo[1,4]dioxin-5-yl)-propionic acid；3-(1,4-benzodioxan-5-yl)propionic acid；3-(2,3-dihydro-1,4-benzodioxin-5-yl)propanoic acid
• CAS: 214895-00-8
• 化学式: C₁₁H₁₂O₄
• 分子量: 208.214
• InChiKey: GHFKRCCBOMTLMF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  甲胺 、 3-(2,3-dihydro-1,4-benzodioxin-5-yl)propionic acid 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 以78%的产率得到N-methyl-[3-(2,3-dihydro-1,4-benzodioxin-5-yl)]propanamide
  参考文献：
  名称：

  Synthesis and Biological Activity of New Melatonin Receptor Ligands

  摘要：

  DOI：

  10.1211/146080800128735638
• 作为产物：
  描述：

  ethyl 3-(2,3-dihydro-1,4-benzodioxin-5-yl)propionate 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 2.0h， 以91%的产率得到3-(2,3-dihydro-1,4-benzodioxin-5-yl)propionic acid
  参考文献：
  名称：

  Synthesis and Biological Activity of New Melatonin Receptor Ligands

  摘要：

  DOI：

  10.1211/146080800128735638

文献信息

• Novel heteroaryl derivatives, their preparation and use
  申请人：H. Lundbeck A/S

  公开号：US20030050306A1

  公开（公告）日：2003-03-13

  A heteroaryl derivative having the formula (I) 1 any of its enantiomers or any mixture thereof, wherein X is —O—, —S—, or CR 4 R 5 —; and Y is —CR 6 R 7 ; —CR 6 R 7 —CR 8 R 9 —, or —CR 6 —CR 7 ; or X and Y together form a group —CR 4 ═R 5 —, or —CR 4 ═CR 5 —CR 6 R 7 —; Z is —O—, or —S—; W is N, C, or CH; n is 2, 3, 4, 5, 6, 7, 8, 9 or 10; m is 2 or 3; A is O or S wherein the doted lines mean an optional bond. The compounds of the invention are considered useful for the treatment of affective disorders such as general anxiety disorder, panic disorder, obsessive compulsive disorder, depression, social phobia and eating disorders, and neurological disorders such as psychosis.

  具有以下结构式(I)的杂环芳基衍生物，其中X为—O—、—S—或CR4R5—；Y为—CR6R7、—CR6R7—CR8R9—或—CR6—CR7；或者X和Y一起形成一个基团—CR4═R5—或—CR4═CR5—CR6R7—；Z为—O—或—S—；W为N、C或CH；n为2、3、4、5、6、7、8、9或10；m为2或3；A为O或S，其中点线表示可选键。该发明的化合物被认为对治疗情感障碍，如广泛性焦虑障碍、恐慌障碍、强迫症、抑郁症、社交恐惧症和进食障碍，以及神经症如精神病等是有用的。
• Benzofuran derivatives, their preparation and use
  申请人：H. Lundbeck A/S

  公开号：US20020032205A1

  公开（公告）日：2002-03-14

  The present invention relates to benzofuran derivatives having general Formula (I) 1 wherein A is selected from (1), (2), (3), (4) 2 wherein Z is O or S; s is 0 or 1; q is 0 or 1; R 4 is hydrogen, C 1-6 -alkyl, C 2-6 -alkenyl, C 2 6 -alkynyl, C 1-6 -alkyl-aryl, or C 1-6 -alkyl-O-aryl; D is a spacer group selected from branched or straight chain C 1-6 -alkylene, C 2-6 -alkenylene and C 2-6 -alkynylene; its enantiomers, and pharmaceutically acceptable acid addition salt thereof. The compounds are potently binding to the 5-HT 1A receptor.

  本发明涉及具有一般式(I)的苯并呋喃衍生物，其中A从(1)，(2)，(3)，(4)中选择，其中Z为O或S；s为0或1；q为0或1；R4为氢，C1-6-烷基，C2-6烯基，C2-6炔基，C1-6烷基-芳基或C1-6烷基-O-芳基；D是从支链或直链C1-6-烷基，C2-6-烯基和C2-6-炔基中选择的间隔基；其对映体和药学上可接受的酸加成盐。这些化合物具有与5-HT1A受体的强结合能力。
• CHROMANE DERIVATIVES AS TRPV3 MODULATORS
  申请人：Lingam V S Prasadarao

  公开号：US20100311778A1

  公开（公告）日：2010-12-09

  The present invention provides transient receptor potential vanilloid (TRPV) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPV3. Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPV3.

  本发明提供了暂时性受体电位香草醛(TRPV)调节剂。特别地，本文所描述的化合物对于治疗或预防由TRPV3调节的疾病、状况和/或疾病非常有用。此外，本文还提供了制备所述化合物的过程、用于其合成的中间体、其制药组合物以及治疗或预防由TRPV3调节的疾病、状况和/或疾病的方法。
• Isoquinoline aminopyrazole derivatives
  申请人：Chen Li

  公开号：US20070179151A1

  公开（公告）日：2007-08-02

  The present invention relates to the compounds of formula I: their pharmaceutically acceptable salts or esters, enantiomeric forms, diastereoisomers and racemates, the preparation of such compounds, pharmaceutical compositions containing them and their manufacture, as well as the use of such compounds in the control or prevention of illnesses such as cancer.

  本发明涉及式I的化合物：其药学上可接受的盐或酯，对映体形式，非对映异构体和外消旋体，以及制备这些化合物，含有它们的制药组合物和其制造，以及在控制或预防癌症等疾病中使用这些化合物的用途。
• Chromane derivatives as TRPV3 modulators
  申请人：Lingam V S Prasadarao

  公开号：US08487121B2

  公开（公告）日：2013-07-16

  The present invention provides transient receptor potential vanilloid (TRPV) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPV3. Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPV3.

  本发明提供了暂时性受体电位香草醛（TRPV）调节剂。特别地，本文描述的化合物可用于治疗或预防由TRPV3调节的疾病、状况和/或障碍。本文还提供了制备本文所述化合物的过程、用于它们合成的中间体、它们的制药组合物以及治疗或预防由TRPV3调节的疾病、状况和/或障碍的方法。