N-BOC-2-(3-吡啶基)-氨基乙酸乙酯 | 313490-93-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: N-BOC-2-(3-吡啶基)-氨基乙酸乙酯
• 英文名称: (RS)-ethyl 2-(t-butoxycarbonylamino)-2-(pyridin-3-yl)acetate
• 英文别名: ethyl 2-(tert-butoxycarbonylamino)-2-(pyridine-3-yl)acetate；Ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-3-yl)acetate；ethyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-pyridin-3-ylacetate
• CAS: 313490-93-6
• 化学式: C₁₄H₂₀N₂O₄
• 分子量: 280.324
• InChiKey: VHBFGPXTGYELDR-UHFFFAOYSA-N

物化性质

• 沸点：
  416.7±40.0 °C(Predicted)
• 密度：
  1.132±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  20
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  77.5
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  N-BOC-2-(3-吡啶基)-氨基乙酸乙酯 在 水 、 O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate 、 potassium hydroxide 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 生成 (RS)-N-benzyl 2-N-(t-butoxycarbonyl)amino-2-(pyridin-3-yl)acetamide
  参考文献：
  名称：

  Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides

  摘要：

  N-Benzyl 2-acetamido-2-substituted acetamides, where the 2-substituent is a (hetero) aromatic moiety, are potent anticonvulsants. We report the synthesis and whole animal pharmacological evaluation of 16 analogues where the terminal 2-acetyl group was removed to give the corresponding primary amino acid derivatives (PAADs). Conversion to the PAAD structure led to a substantial drop in seizure protection in animal tests, demonstrating the importance of the N-acetyl moiety for anticonvulsant activity. However, several of the PAADs displayed notable pain-attenuating activities in a mouse model. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.04.002
• 作为产物：
  描述：

  3-吡啶乙酸乙酯 在 甲酸 、 亚硝酸特丁酯 、 sodium ethanolate 、 锌 作用下， 以 甲醇 、 乙醇 、 二氯甲烷 、 水 为溶剂， 反应 36.0h， 生成 N-BOC-2-(3-吡啶基)-氨基乙酸乙酯
  参考文献：
  名称：

  Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides

  摘要：

  N-Benzyl 2-acetamido-2-substituted acetamides, where the 2-substituent is a (hetero) aromatic moiety, are potent anticonvulsants. We report the synthesis and whole animal pharmacological evaluation of 16 analogues where the terminal 2-acetyl group was removed to give the corresponding primary amino acid derivatives (PAADs). Conversion to the PAAD structure led to a substantial drop in seizure protection in animal tests, demonstrating the importance of the N-acetyl moiety for anticonvulsant activity. However, several of the PAADs displayed notable pain-attenuating activities in a mouse model. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.04.002

文献信息

• [EN] 3,4-DISUBSTITUTED OXAZOLIDINONE DERIVATIVES AND THEIR USE AS INHIBITORS OF THE CALCIUM ACTIVATED POTASSIUM CHANNEL<br/>[FR] DÉRIVÉS D'OXAZOLIDINONE 3,4-DISUBSTITUÉE ET LEUR UTILISATION COMME INHIBITEURS DES CANAUX POTASSIQUES ACTIVÉS PAR LE CALCIUM
  申请人：HOFFMANN LA ROCHE

  公开号：WO2014067861A1

  公开（公告）日：2014-05-08

  The invention provides compounds having the general formula I wherein n, R1, R2a, R2b, R3a and R3b are as herein defined., composition comprising the compounds and methods of using the compounds.

  这项发明提供了具有一般式I的化合物，其中n、R1、R2a、R2b、R3a和R3b的定义如本文所述。包括这些化合物的组合物以及使用这些化合物的方法。
• NOVEL OXAZOLIDINONE COMPOUNDS
  申请人：Hoffmann-La Roche Inc.

  公开号：US20150246894A1

  公开（公告）日：2015-09-03

  The invention provides compounds having the general formula I wherein n, R 1 , R 2a , R 2b , R 3a and R 3b are as herein defined, composition comprising the compounds and methods of using the compounds.

  本发明提供具有一般式I的化合物，其中n，R1，R2a，R2b，R3a和R3b的定义如下，包括上述化合物的组合物和使用该化合物的方法。
• 3,4-DISUBSTITUTED OXAZOLIDINONE DERIVATIVES AND THEIR USE AS INHIBITORS OF THE CALCIUM ACTIVATED POTASSIUM CHANNEL
  申请人：F.Hoffmann-La Roche AG

  公开号：EP2912034A1

  公开（公告）日：2015-09-02
• US9611232B2
  申请人：——

  公开号：US9611232B2

  公开（公告）日：2017-04-04
• Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides
  作者：Pranjal K. Baruah、Jason Dinsmore、Amber M. King、Christophe Salomé、Marc De Ryck、Rafal Kaminski、Laurent Provins、Harold Kohn

  DOI：10.1016/j.bmc.2012.04.002

  日期：2012.6

  N-Benzyl 2-acetamido-2-substituted acetamides, where the 2-substituent is a (hetero) aromatic moiety, are potent anticonvulsants. We report the synthesis and whole animal pharmacological evaluation of 16 analogues where the terminal 2-acetyl group was removed to give the corresponding primary amino acid derivatives (PAADs). Conversion to the PAAD structure led to a substantial drop in seizure protection in animal tests, demonstrating the importance of the N-acetyl moiety for anticonvulsant activity. However, several of the PAADs displayed notable pain-attenuating activities in a mouse model. (C) 2012 Elsevier Ltd. All rights reserved.