benzyl 4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate | 777089-58-4

• 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: benzyl 4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate
• 英文别名: benzyl N-[4-[(E)-3-hydroxyprop-1-enyl]phenyl]carbamate
• CAS: 777089-58-4
• 化学式: C₁₇H₁₇NO₃
• 分子量: 283.327
• InChiKey: QEQGTBWEEXUOMT-QPJJXVBHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  21
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  benzyl 4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate 在 bis(N-tert-butylsalicylaldiminato)copper(II) 锂硼氢 、 正丁基锂 、 1-氯-N,N,2-三甲基丙烯胺 、 甲基磺酰氯 作用下， 以 四氢呋喃 、 二氯甲烷 、 1,2-二氯乙烷 、 甲苯 为溶剂， 反应 0.67h， 生成 [(1S,5R,6S)-4-(3-Oxa-bicyclo[3.1.0]hex-6-yl)-phenyl]-carbamic acid benzyl ester
  参考文献：
  名称：

  Synthesis of Aza-, Oxa-, and Thiabicyclo[3.1.0]hexane Heterocycles from a Common Synthetic Intermediate

  摘要：

  An efficient and stereospecific approach to the synthesis of structurally constrained aza-, oxa-, and thiabicyclo[3.1.0]hexane heterocycles has been achieved through application of the intramolecular cyclopropanation reaction of diazoacetates. The various constrained heterocycles (X = N, O, or S) are conveniently prepared from a common diol intermediate accessible from readily available cinnamyl alcohols. Application of the methodology to the synthesis of conformationally constrained oxazolidinone antibacterials is also discussed.

  DOI：

  10.1021/ol050730h
• 作为产物：
  描述：

  4-溴苯基氨基甲酸苄酯 在 lithium aluminium tetrahydride 、 正丁基锂 、 sodium hydride 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 20.83h， 生成 benzyl 4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate
  参考文献：
  名称：

  Synthesis of Aza-, Oxa-, and Thiabicyclo[3.1.0]hexane Heterocycles from a Common Synthetic Intermediate

  摘要：

  An efficient and stereospecific approach to the synthesis of structurally constrained aza-, oxa-, and thiabicyclo[3.1.0]hexane heterocycles has been achieved through application of the intramolecular cyclopropanation reaction of diazoacetates. The various constrained heterocycles (X = N, O, or S) are conveniently prepared from a common diol intermediate accessible from readily available cinnamyl alcohols. Application of the methodology to the synthesis of conformationally constrained oxazolidinone antibacterials is also discussed.

  DOI：

  10.1021/ol050730h

文献信息

• [EN] ANTIMICROBIAL [3.1.0] BICYCLOHEXYLPHENYL-OXAZOLIDINONE DERIVATIVES AND ANALOGUES<br/>[FR] DERIVES DE [3.1.0] BICYCLOHEXYLPHENYL-OXAZOLIDINONE ANTIMICROBIENS ET LEURS ANALOGUES
  申请人：UPJOHN CO

  公开号：WO2004089943A1

  公开（公告）日：2004-10-21

  The present invention provides certain [3.1.0] bicyclic oxazolidinone derivatives of Formula (I) or pharmaceutically acceptable salts or prodrugs thereof that are antibacterial agents, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.

  本发明提供了具有抗菌作用的某些[3.1.0]双环氧唑啉酮衍生物的化合物，其化学式为(I)，或其药用可接受的盐或前药，包含它们的药物组合物，使用它们的方法，以及制备这些化合物的方法。
• Antimicrobial [3.1.0] bicyclohexylphenyl-oxazolidinone derivatives and analogues
  申请人：Renslo Adam

  公开号：US20050192325A1

  公开（公告）日：2005-09-01

  The present invention provides certain [3.1.0] bicyclic oxazolidinone derivatives of formula I or pharmaceutically acceptable salts or prodrugs thereof that are antibacterial agents, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.

  本发明提供了某些[3.1.0]双环氧唑啉衍生物I的化合物，或其药学上可接受的盐或前药，这些化合物是抗菌剂，含有它们的制药组合物，它们的使用方法以及制备这些化合物的方法。
• ANTIMICROBIAL [3.1.0] BICYCLOHEXYLPHENYL- OXAZOLIDINONE DERIVATIVES AND ANALOGUES
  申请人：Renslo Adam

  公开号：US20080090884A1

  公开（公告）日：2008-04-17

  The present invention provides certain [3.1.0]bicyclic oxazolidinone derivatives of Formula I I or pharmaceutically acceptable salts or prodrugs thereof that are antibacterial agents, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.

  本发明提供了某些[3.1.0]双环氧唑啉衍生物II式或其药学上可接受的盐或前药，它们是抗菌剂，包括含有它们的制药组合物，使用它们的方法，以及制备这些化合物的方法。
• US7279494B2
  申请人：——

  公开号：US7279494B2

  公开（公告）日：2007-10-09
• Synthesis of Aza-, Oxa-, and Thiabicyclo[3.1.0]hexane Heterocycles from a Common Synthetic Intermediate
  作者：Adam R. Renslo、Hongwu Gao、Priyadarshini Jaishankar、Revathy Venkatachalam、Mikhail F. Gordeev

  DOI：10.1021/ol050730h

  日期：2005.6.1

  An efficient and stereospecific approach to the synthesis of structurally constrained aza-, oxa-, and thiabicyclo[3.1.0]hexane heterocycles has been achieved through application of the intramolecular cyclopropanation reaction of diazoacetates. The various constrained heterocycles (X = N, O, or S) are conveniently prepared from a common diol intermediate accessible from readily available cinnamyl alcohols. Application of the methodology to the synthesis of conformationally constrained oxazolidinone antibacterials is also discussed.