methyl 3-[2-(1-pyrrolidinyl)ethoxy]benzoate | 262425-12-7

• 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: methyl 3-[2-(1-pyrrolidinyl)ethoxy]benzoate
• 英文别名: methyl 3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzoate；Methyl-3-(2-pyrrolidin-1-yl)ethoxy Benzoate；methyl 3-(2-pyrrolidin-1-ylethoxy)benzoate
• CAS: 262425-12-7
• 化学式: C₁₄H₁₉NO₃
• 分子量: 249.31
• InChiKey: LUDOJQMXCRXYSC-UHFFFAOYSA-N

物化性质

• 沸点：
  370.6±22.0 °C(Predicted)
• 密度：
  1.114±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  18
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  38.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl 3-[2-(1-pyrrolidinyl)ethoxy]benzoate 在 水 、 sodium hydroxide 、 盐酸 作用下， 以 甲醇 、 水 为溶剂， 反应 18.0h， 生成 3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzoic acid
  参考文献：
  名称：

  [EN] ASK1 INHIBITING PYRROLOPYRIMIDINE DERIVATIVES
  [FR] DÉRIVÉS PYRROLOPYRIMIDINE INHIBANT ASK1

  摘要：

  这项发明涉及式(I)的吡咯吡嘧啶衍生物：其中R1、X、p、R4、R2和R3如本文所定义，并且它们作为药物的用途。

  公开号：

  WO2012080735A1
• 作为产物：
  描述：

  N-(2-羟乙基)-吡咯烷 在 氯化亚砜 、 potassium carbonate 、 potassium iodide 作用下， 以 氯仿 、 丙酮 为溶剂， 反应 49.0h， 生成 methyl 3-[2-(1-pyrrolidinyl)ethoxy]benzoate
  参考文献：
  名称：

  [EN] ASK1 INHIBITING PYRROLOPYRIMIDINE DERIVATIVES
  [FR] DÉRIVÉS PYRROLOPYRIMIDINE INHIBANT ASK1

  摘要：

  这项发明涉及式(I)的吡咯吡嘧啶衍生物：其中R1、X、p、R4、R2和R3如本文所定义，并且它们作为药物的用途。

  公开号：

  WO2012080735A1

文献信息

• Pyruvamide Compounds as Inhibitors of Dust Mite Group 1 Peptidase Allergen and Their Use
  申请人：Robinson Clive

  公开号：US20120322722A1

  公开（公告）日：2012-12-20

  The present invention pertains generally to the field of therapeutic compounds and more specifically to certain pyruvamide compounds of the formula (X) (for convenience, collectively referred to herein as “PVA compounds”), which, inter alia, inhibit a dust mite Group 1 peptidase allergen (e.g., Der p 1, Der f 1, Eur m 1). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit a dust mite Group 1 peptidase allergen, and in the treatment of diseases and disorders that are mediated by a dust mite Group 1 peptidase allergen; that are ameliorated by the inhibition of a dust mite Group 1 peptidase allergen; asthma; rhinitis; allergic conjunctivitis; atopic dermatitis; an allergic condition which is triggered by dust mites; an allergic condition which is triggered by a dust mite Group 1 peptidase allergen; and canine atopy.

  本发明一般涉及治疗化合物领域，更具体地涉及某些丙酮酰胺化合物的公式（X）（为方便起见，以下统称为“PVA化合物”），该化合物在某些情况下抑制尘螨1组蛋白酶过敏原（例如Der p 1、Der f 1、Eur m 1）。本发明还涉及包含这种化合物的药物组合物，以及在体外和体内使用这种化合物和组合物来抑制尘螨1组蛋白酶过敏原，并用于治疗由尘螨1组蛋白酶过敏原介导的疾病和疾病，通过抑制尘螨1组蛋白酶过敏原而得到缓解的疾病和疾病；哮喘；鼻炎；过敏性结膜炎；特应性皮炎；由尘螨引发的过敏症状；由尘螨1组蛋白酶过敏原引发的过敏症状；以及犬类特应性。
• ASK 1 INHIBITING PYRROLOPYRIMIDINE DERIVATIVES
  申请人：Witty David R.

  公开号：US20140038957A1

  公开（公告）日：2014-02-06

  This invention relates to pyrrolopyrimidine derivatives of formula (I): where R 1 , X, p, R 4 , R 2 and R 3 are as defined herein, and their use as pharmaceuticals.

  本发明涉及公式（I）的吡咯吡嘧啶衍生物：其中R1、X、p、R4、R2和R3如本文所定义，并且它们作为药物的用途。
• ASK 1 inhibiting pyrrolopyrimidine derivatives
  申请人：Witty David R.

  公开号：US09045485B2

  公开（公告）日：2015-06-02

  This invention relates to pyrrolopyrimidine derivatives of formula (I): where R1, X, p, R4, R2 and R3 are as defined herein, and their use as pharmaceuticals.

  本发明涉及式（I）的吡咯吡咪啉衍生物：其中R1，X，p，R4，R2和R3如本文所定义，并且它们的用途为药物。
• Diamino Benzo[<i>b</i>]thiophene Derivatives as a Novel Class of Active Site Directed Thrombin Inhibitors. 5. Potency, Efficacy, and Pharmacokinetic Properties of Modified C-3 Side Chain Derivatives
  作者：Daniel J. Sall、Dianna L. Bailey、Jolie A. Bastian、John A. Buben、Nickolay Y. Chirgadze、Amy C. Clemens-Smith、Michael L. Denney、Matthew J. Fisher、Deborah D. Giera、Donetta S. Gifford-Moore、Richard W. Harper、Lea M. Johnson、Valentine J. Klimkowski、Todd J. Kohn、Ho-Shen Lin、Jefferson R. McCowan、Alan D. Palkowitz、Michael E. Richett、Gerald F. Smith、David W. Snyder、Kumiko Takeuchi、John E. Toth、Minsheng Zhang

  DOI：10.1021/jm9903388

  日期：2000.2.1

  A systematic investigation of the structure-activity relationships of the C-3 side chain of the screening hit la led to the identification of the potent thrombin inhibitors 23c, 28c, and 31c. Their activities (1240, 903, and 1271 x 10(6) L/mol, respectively) represent 2200- and 2900-fold increases in potency over the starting lead la. This activity enhancement was accomplished with an increase of thrombin selectivity. The in vitro anticoagulant profiles of derivatives 28c and 31c were determined, and they compare favorably with the clinical agent H-R-1-[4aS,-8aS]perhydroisoquinolyl-prolyl-arginyl aldehyde (D-Piq-Pro-Arg-H; 32). The more potent members of this series have been studied in an arterial/venous shunt (AV shunt) model of thrombosis and were found to be efficacious in reducing clot formation. However, their efficacy is currently limited by their rapid and extensive distribution following administration.
• PYRUVAMIDE COMPOUNDS AS INHIBITORS OF DUST MITE GROUP 1 PEPTIDASE ALLERGEN
  申请人：St. George's Hospital Medical School

  公开号：EP2526116B1

  公开（公告）日：2015-05-13