1-Benzyl-3-(4-methoxybenzenesulfonyl)-piperidine-3-carboxylic acid | 352209-84-8

• 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: 1-Benzyl-3-(4-methoxybenzenesulfonyl)-piperidine-3-carboxylic acid
• 英文别名: 1-Benzyl-3-(4-methoxyphenyl)sulfonylpiperidine-3-carboxylic acid
• CAS: 352209-84-8
• 化学式: C₂₀H₂₃NO₅S
• 分子量: 389.472
• InChiKey: YTUWNDZXNDHFKZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  27
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  92.3
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  1-Benzyl-3-(4-methoxybenzenesulfonyl)-piperidine-3-carboxylic acid 在 草酰氯 、 N,N-二甲基甲酰胺 、 三乙胺 作用下， 以91%的产率得到1-benzyl-N-hydroxy-3-(4-methoxyphenyl)sulfonylpiperidine-3-carboxamide
  参考文献：
  名称：

  An efficient method to prepare α-sulfonyl hydroxamic acid derivatives

  摘要：

  alpha -Sulfonyl hydroxamic acid derivatives are biologically important molecules. An efficient protocol has bt en developed to mal;e these molecules via a direct sulfonylation of enolates. Several piperidine containing alpha -sulfonyl hydroxamic acid compounds have been prepared by this procedure. (C) 2001 Published by Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4039(01)00835-8
• 作为产物：
  描述：

  4-甲氧基苯磺酰氟 在 盐酸 、 lithium hydroxide 、 三乙胺 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 水 为溶剂， 反应 5.5h， 生成 1-Benzyl-3-(4-methoxybenzenesulfonyl)-piperidine-3-carboxylic acid
  参考文献：
  名称：

  An efficient method to prepare α-sulfonyl hydroxamic acid derivatives

  摘要：

  alpha -Sulfonyl hydroxamic acid derivatives are biologically important molecules. An efficient protocol has bt en developed to mal;e these molecules via a direct sulfonylation of enolates. Several piperidine containing alpha -sulfonyl hydroxamic acid compounds have been prepared by this procedure. (C) 2001 Published by Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4039(01)00835-8

文献信息

• Method for preparing alpha-sulfonyl hydroxamic acid derivatives
  申请人：——

  公开号：US20020099035A1

  公开（公告）日：2002-07-25

  Compounds of the formula: 1 that can be important as matrix metalloproteinase (MMP) and TNF-alpha converting enzyme (TACE) inhibitors, phosphodiesterase inhibitors, renin inhibitors, antithrombotics, and 5 -lipoxygenase inhibitors are prepared by novel methods of the present invention.

  该公式的化合物： 可以作为基质金属蛋白酶（MMP）和TNF-alpha转化酶（TACE）抑制剂、磷酸二酯酶抑制剂、肾素抑制剂、抗血栓药物和5-脂氧合酶抑制剂的重要化合物，通过本发明的新方法制备。
• [EN] METHOD FOR PREPARING ALPHA-SULFONYL HYDROXAMIC ACID DERIVATIVES<br/>[FR] PROCEDE POUR LA PREPARATION DE DERIVES D'ACIDE HYDROXAMIQUE ALPHA-SULFONYLE
  申请人：AMERICAN CYANAMID CO

  公开号：WO2001055112A1

  公开（公告）日：2001-08-02

  Compounds of the formula (I) that can be important as matrix metalloproteinase (MMP) and TNF-alpha converting enzyme (TACE) inhibitors, phosphodiesterase inhibitors, renin inhibitors, antithrombotics, and 5-lipoxygenase inhibitors are prepared by novel methods of the present invention.

  本发明的新方法制备出式(I)的化合物，这些化合物可以作为基质金属蛋白酶(MMP)和TNF-alpha转换酶(TACE)抑制剂、磷酸二酯酶抑制剂、肾素抑制剂、抗血栓剂和5-脂氧合酶抑制剂。
• METHOD FOR PREPARING ALPHA-SULFONYL HYDROXAMIC ACID DERIVATIVES
  申请人：American Cyanamid Company

  公开号：EP1252143A1

  公开（公告）日：2002-10-30
• An efficient method to prepare α-sulfonyl hydroxamic acid derivatives
  作者：Vincent P Sandanayaka、Arie Zask、Aranapakam M Venkatesan、Jannie Baker

  DOI：10.1016/s0040-4039(01)00835-8

  日期：2001.7

  alpha -Sulfonyl hydroxamic acid derivatives are biologically important molecules. An efficient protocol has bt en developed to mal;e these molecules via a direct sulfonylation of enolates. Several piperidine containing alpha -sulfonyl hydroxamic acid compounds have been prepared by this procedure. (C) 2001 Published by Elsevier Science Ltd.