methyl 1-benzyl-4-hydroxy-3-pyrrolin-2-one-3-carboxylate | 216175-01-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯啉
• 英文名称: methyl 1-benzyl-4-hydroxy-3-pyrrolin-2-one-3-carboxylate
• 英文别名: 1-benzyl-4-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-3-carboxylic acid methyl ester；methyl 1-benzyl-3-hydroxy-5-oxo-2H-pyrrole-4-carboxylate
• CAS: 216175-01-8
• 化学式: C₁₃H₁₃NO₄
• 分子量: 247.251
• InChiKey: XPMBLMWAENTMTO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  66.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl 1-benzyl-4-hydroxy-3-pyrrolin-2-one-3-carboxylate 在 palladium on activated charcoal air 、 氢气 、 manganese triacetate 作用下， 以 二氯甲烷 、 溶剂黄146 为溶剂， 23.0~40.0 ℃ 、5.07 MPa 条件下， 反应 1.0h， 生成 (3aS,6aS)-5-Benzyl-6a-hydroxy-4-oxo-2,2-diphenyl-hexahydro-furo[2,3-c]pyrrole-3a-carboxylic acid methyl ester
  参考文献：
  名称：

  钯催化的氮杂双环过氧化物的氢解。定量转化为1-羟基-7-氮杂-2-氧杂双环[3.3.0]辛烷

  摘要：

  钯催化的1-羟基-8-氮杂-2,3-二氧杂双环[4.3.0]壬烷的钯催化还原反应很容易通过吡咯烷二酮的锰（III）介导的氧化式[2 + 2 + 2]环加成反应获得与烯烃和分子氧的衍生物导致过氧化物氧之一的正式挤出，并以定量的化学收率产生了1-羟基-7-氮杂-2-氧杂双环[3.3.0]辛烷。

  DOI：

  10.1016/s0040-4039(99)00604-8
• 作为产物：
  描述：

  N-苄基甘氨酸 在 sodium alkoxide 作用下， 生成 methyl 1-benzyl-4-hydroxy-3-pyrrolin-2-one-3-carboxylate
  参考文献：
  名称：

  Chowdhury, Firoz Alam; Nishino, Hiroshi; Kurosawa, Kazu, Heterocycles, 1999, vol. 51, # 3, p. 575 - 591

  摘要：

  DOI：

文献信息

• One-pot synthesis of azabicyclic peroxides from tetramic acid derivatives by manganese(III)-mediated oxidative [2+2+2]cycloaddition
  作者：Firoz Alam Chowdhury、Hiroshi Nishino、Kazu Kurosawa

  DOI：10.1016/s0040-4039(98)01765-1

  日期：1998.10

  A simple azabicyclic peroxide synthesis was achieved by the manganese(III)-mediated oxidative formal [2+2+2] cycloaddition. A mixture of tetramic acid derivatives and alkenes was oxidized with manganese(III) acetate under a dry air stream to give 1-hydroxy-8-aza-2,3-dioxabicyclo[4.3.0]nonan-7-ones in good to quantitative chemical yields.

  一个简单的氮杂双环过氧化物合成是通过锰（III）介导的氧化式[2 + 2 + 2]环加成反应实现的。在干燥空气流下，用乙酸锰（III）氧化四酸衍生物和烯烃的混合物，得到定量至良好的1-羟基-8-氮杂-2,3-二氧杂双环[4.3.0]壬南-7-酮。化学收率。
• INHIBITORS OF UNDECAPRENYL PYROPHOSPHATE SYNTHASE
  申请人：Hurley Timothy Brian

  公开号：US20090203694A1

  公开（公告）日：2009-08-13

  The present invention relates to compounds that are selective and/or potent inhibitors of UPPS. In addition to compounds which inhibit UPPS, the invention also provides pharmaceutical compositions comprising these compounds and methods of using these compounds for treating bacterial disease, such as bacterial infection.

  本发明涉及一种选择性和/或强效抑制UPPS的化合物。除了抑制UPPS的化合物外，本发明还提供包含这些化合物的药物组合物以及使用这些化合物治疗细菌性疾病（如细菌感染）的方法。
• Design and structure–activity relationships of potent and selective inhibitors of undecaprenyl pyrophosphate synthase (UPPS): Tetramic, tetronic acids and dihydropyridin-2-ones
  作者：Stefan Peukert、Yingchuan Sun、Rui Zhang、Brian Hurley、Mike Sabio、Xiaoyu Shen、Christen Gray、JoAnn Dzink-Fox、Jianshi Tao、Regina Cebula、Sompong Wattanasin

  DOI：10.1016/j.bmcl.2008.02.009

  日期：2008.3

  Based on a pharmacophore hypothesis substituted tetramic and tetronic acid 3-carboxamides as well as dihydropyridin-2-one- 3-carboxamides were investigated as inhibitors of undecaprenyl pyrophosphate synthase (UPPS) for use as novel antimicrobial agents. Synthesis and structure - activity relationship patterns for this class of compounds are discussed. Selectivity data and antibacterial activities for selected compounds are provided. (C) 2008 Elsevier Ltd. All rights reserved.
• Design, synthesis and In vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1
  作者：Adrian Folkes、S.David Brown、Lynne E. Canne、Jocelyn Chan、Erin Engelhardt、Sergey Epshteyn、Richard Faint、Julian Golec、Art Hanel、Patrick Kearney、James W. Leahy、Morrison Mac、David Matthews、Michael P. Prisbylla、Jason Sanderson、Reyna J. Simon、Zerom Tesfai、Nigel Vicker、Shouming Wang、Robert R. Webb、Peter Charlton

  DOI：10.1016/s0960-894x(02)00078-1

  日期：2002.4

  We have synthesized and evaluated a series of tetramic acid-based and hydroxvquinolinone-based inhibitors of plasminogen activator inhibitor-1 (PAI-1). These studies resulted in the identification of several compounds which showed excellent potency against PAI-1. The design, synthesis and SAR of these compounds are described. (C) 2002 Elsevier Science Ltd. All rights reserved.