ethyl 1-cyclopropyl-4-[(4-fluorophenyl)sulfonyl]piperidine-4-carboxylate | 226399-90-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: ethyl 1-cyclopropyl-4-[(4-fluorophenyl)sulfonyl]piperidine-4-carboxylate
• 英文别名: ethyl N-cyclopropyl-4-(4-fluorophenylsulfonyl]-4-piperidinecarboxylate；Ethyl 1-cyclopropyl-4-(4-fluorophenyl)sulfonylpiperidine-4-carboxylate
• CAS: 226399-90-2
• 化学式: C₁₇H₂₂FNO₄S
• 分子量: 355.43
• InChiKey: BGLYEXHYDABRGM-UHFFFAOYSA-N

物化性质

• 沸点：
  479.5±45.0 °C(Predicted)
• 密度：
  1.324±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  24
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  ethyl 1-cyclopropyl-4-[(4-fluorophenyl)sulfonyl]piperidine-4-carboxylate 在 lithium hydroxide 、 盐酸 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 72.0h， 以78.2%的产率得到1-Cyclopropyl-4-(4-fluorophenyl)sulfonylpiperidine-4-carboxylic acid
  参考文献：
  名称：

  Aromatic sulfone hydroxamates and their use as protease inhibitors

  摘要：

  这项发明涉及芳香砜羟肟酸酯（也称为“芳香砜羟肟酸”）及其盐，该化合物在抑制基质金属蛋白酶（也称为“基质金属蛋白酶”或“MMP”）活性和/或聚集素酶活性方面具有作用。该发明还涉及一种预防或治疗方法，包括向动物，特别是患有（或易患）与MMP和/或聚集素酶活性相关的病理状况的哺乳动物，施用此类化合物或盐以达到抑制MMP和/或聚集素酶的有效量。

  公开号：

  US20040010019A1
• 作为产物：
  描述：

  ethyl 4-(4-fluorophenylsulfonyl)piperidine-4-carboxylate hydrochloride 、 1-乙氧基-1-三甲硅氧基环丙烷 在 sodium tetrahydroborate 、 4 A molecular sieve 、 溶剂黄146 作用下， 以 甲醇 为溶剂， 反应 6.0h， 以88.8%的产率得到ethyl 1-cyclopropyl-4-[(4-fluorophenyl)sulfonyl]piperidine-4-carboxylate
  参考文献：
  名称：

  Aromatic sulfone hydroxamates and their use as protease inhibitors

  摘要：

  这项发明涉及芳香砜羟肟酸酯（也称为“芳香砜羟肟酸”）及其盐，该化合物在抑制基质金属蛋白酶（也称为“基质金属蛋白酶”或“MMP”）活性和/或聚集素酶活性方面具有作用。该发明还涉及一种预防或治疗方法，包括向动物，特别是患有（或易患）与MMP和/或聚集素酶活性相关的病理状况的哺乳动物，施用此类化合物或盐以达到抑制MMP和/或聚集素酶的有效量。

  公开号：

  US20040010019A1

文献信息

• Aromatic sulfone hydroxamic acids and their use as protease inhibitors
  申请人：——

  公开号：US20030073718A1

  公开（公告）日：2003-04-17

  This invention is directed to aromatic sulfone hydroxamates (also known as aromatic sulfone hydroxamic acids) and salts thereof that, inter alia, tend to inhibit matrix metalloproteinase (also known as matrix metalloprotease or MMP) activity and/or aggrecanase activity. This invention also is directed to a treatment method that comprises administering such a compound or salt in an MMP-inhibiting and/or aggrecanase-inhibiting effective amount to an animal, particularly a mammal having (or disposed to having) a pathological condition associated with MMP activity and/or aggrecanase activity.

  本发明涉及芳香基磺酮羟肟酸（也称为芳香基磺酮羟肟酸）及其盐，该化合物在抑制基质金属蛋白酶（也称为基质金属蛋白酶或MMP）活性和/或聚集素酶（aggrecanase）活性方面具有倾向性。本发明还涉及一种治疗方法，其包括向动物，特别是患有（或有病理条件与MMP活性和/或聚集素酶活性相关的）哺乳动物中，以MMP抑制剂和/或聚集素酶抑制剂有效量的该化合物或盐进行治疗。
• AROMATIC SULFONE HYDROXAMIC ACID METALLOPROTEASE INHIBITOR
  申请人：——

  公开号：US20010014688A1

  公开（公告）日：2001-08-16

  A treatment process is disclosed that comprises administering an effective amount of an aromatic sulfone hydroxamic acid that exhibits excellent inhibitory activity of one or more matrix metalloprotease (MMP) enzymes, such as MMP-2, MMP-9 and MMP-13, while exhibiting substantially less inhibition at least of MMP-1 to a host having a condition associated with pathological matrix metalloprotease activity. Also disclosed are metalloprotease inhibitor compounds having those selective activities, processes for manufacture of such compounds and pharmaceutical compositions using an inhibitor.

  本发明涉及一种治疗过程，包括向患有与病理基质金属蛋白酶活性相关的状况的宿主施用有效量的芳香磺酮羟肟酸，该芳香磺酮羟肟酸表现出优异的抑制活性，可抑制一种或多种基质金属蛋白酶(MMP)酶，如MMP-2、MMP-9和MMP-13，同时对MMP-1的抑制显著较少。还揭示了具有这些选择性活性的金属蛋白酶抑制剂化合物、制造这种化合物的工艺以及使用抑制剂的制药组合物。
• Aromatic sulfone hydroxamic acid metalloprotease inhibitor
  申请人：——

  公开号：US20020177588A1

  公开（公告）日：2002-11-28

  A treatment process is disclosed that comprises administering an effective amount of an aromatic sulfone hydroxamic acid that exhibits excellent inhibitory activity of one or more matrix metalloprotease (MMP) enzymes, such as MMP-2, MMP-9 and MMP-13, while exhibiting substantially less inhibition at least of MMP-1 to a host having a condition associated with pathological matrix metalloprotease activity. Also disclosed are metalloprotease inhibitor compounds having those selective activities, processes for manufacture of such compounds and pharmaceutical compositions using an inhibitor.

  本发明揭示了一种治疗过程，包括向患有与病理性基质金属蛋白酶活性相关的病症的宿主施用一种有效量的芳香族磺酰羟肟酸，该芳香族磺酰羟肟酸在MMP-2、MMP-9和MMP-13等一种或多种基质金属蛋白酶（MMP）酶活性上表现出优异的抑制活性，同时在至少MMP-1的抑制上表现出明显较少的抑制。还揭示了具有这些选择性活性的金属蛋白酶抑制剂化合物、制造这种化合物的过程以及使用抑制剂的制药组合物。
• Orally Active MMP-1 Sparing α-Tetrahydropyranyl and α-Piperidinyl Sulfone Matrix Metalloproteinase (MMP) Inhibitors with Efficacy in Cancer, Arthritis, and Cardiovascular Disease
  作者：Daniel P. Becker、Thomas E. Barta、Louis J. Bedell、Terri L. Boehm、Brian R. Bond、Jeffery Carroll、Chris P. Carron、Gary A. DeCrescenzo、Alan M. Easton、John N. Freskos、Chris L. Funckes-Shippy、Marcia Heron、Susan Hockerman、Carol Pearcy Howard、James R. Kiefer、Madeleine H. Li、Karl J. Mathis、Joseph J. McDonald、Pramod P. Mehta、Grace E. Munie、Teresa Sunyer、Craig A. Swearingen、Clara I. Villamil、Dean Welsch、Jennifer M. Williams、Ying Yu、Jun Yao

  DOI：10.1021/jm100669j

  日期：2010.9.23

  alpha-Sulfone-alpha-piperidine and alpha-tetrahydropyranyl hydroxamates were explored that are potent inhibitors of MMP's-2, -9, and -13 that spare MMP-1, with oral efficacy in inhibiting tumor growth in mice and left-ventricular hypertrophy in rats and in the bovine cartilage degradation ex vivo explant system. alpha-Piperidine 19v (SC-78080/SD-2590) was selected for development toward the initial indication of cancer, while alpha-piperidine and alpha-tetrahydropyranyl hydroxamates 19w (SC-77964) and 9l (SC-77774), respectively, were identified as backup compounds.
• MMP-13 selective isonipecotamide α-sulfone hydroxamates
  作者：Stephen A. Kolodziej、Susan L. Hockerman、Gary A. DeCrescenzo、Joseph J. McDonald、Debbie A. Mischke、Grace E. Munie、Theresa R. Fletcher、Nathan Stehle、Craig Swearingen、Daniel P. Becker

  DOI：10.1016/j.bmcl.2010.04.111

  日期：2010.6

  A series of N-aryl isonipecotamide alpha-sulfone hydroxamate derivatives has been prepared utilizing a combination of solution-phase and resin-bound library technologies to afford compounds that are potent and highly selective for MMP-13. (C) 2010 Elsevier Ltd. All rights reserved.