(S)-1-[(2-tert-Butoxycarbonylamino-acetyl)-(4-methoxy-benzyl)-amino]-cyclopent-2-enecarboxylic acid methyl ester | 597540-57-3

• 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
• 英文名称: (S)-1-[(2-tert-Butoxycarbonylamino-acetyl)-(4-methoxy-benzyl)-amino]-cyclopent-2-enecarboxylic acid methyl ester
• 英文别名: methyl (1S)-1-[(4-methoxyphenyl)methyl-[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]amino]cyclopent-2-ene-1-carboxylate
• CAS: 597540-57-3
• 化学式: C₂₂H₃₀N₂O₆
• 分子量: 418.49
• InChiKey: FUCVYPQPMFQWBN-JOCHJYFZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  30
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  94.2
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (S)-1-[(2-tert-Butoxycarbonylamino-acetyl)-(4-methoxy-benzyl)-amino]-cyclopent-2-enecarboxylic acid methyl ester 在 三氟乙酸 、 柠檬酸 、 sodium nitrite 作用下， 以 乙醚 、 二氯甲烷 、 氯仿 、 水 为溶剂， 反应 46.5h， 生成 (2aR,4aS,6aR,6bS)-4-(4-Methoxy-benzyl)-3-oxo-3,4,5,6,6a,6b-hexahydro-2aH-1,2,4-triaza-cyclopenta[cd]pentalene-4a-carboxylic acid methyl ester
  参考文献：
  名称：

  Stereocontrolled synthesis of a potent agonist of group II metabotropic glutamate receptors, (+)-LY354740, and its related derivatives

  摘要：

  Efficient synthesis of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740: 1) and its structurally related analogs (-)-2 and (-)-3 has been accomplished starting with (1S,2R)-1-amino-2-hydroxycyclopentane- or cyclohexanecarboxylic acid (4 or 17) via an intramolecular cyclopropanation of alpha-diazo acetamide. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(03)01316-9
• 作为产物：
  描述：

  (S)-1-Amino-cyclopent-2-enecarboxylic acid methyl ester 在 N-羟基-7-氮杂苯并三氮唑 、 三乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 29.0h， 生成 (S)-1-[(2-tert-Butoxycarbonylamino-acetyl)-(4-methoxy-benzyl)-amino]-cyclopent-2-enecarboxylic acid methyl ester
  参考文献：
  名称：

  Stereocontrolled synthesis of a potent agonist of group II metabotropic glutamate receptors, (+)-LY354740, and its related derivatives

  摘要：

  Efficient synthesis of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740: 1) and its structurally related analogs (-)-2 and (-)-3 has been accomplished starting with (1S,2R)-1-amino-2-hydroxycyclopentane- or cyclohexanecarboxylic acid (4 or 17) via an intramolecular cyclopropanation of alpha-diazo acetamide. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(03)01316-9

文献信息

• Stereocontrolled synthesis of a potent agonist of group II metabotropic glutamate receptors, (+)-LY354740, and its related derivatives
  作者：Yasufumi Ohfune、Takashi Demura、Seiji Iwama、Hiromi Matsuda、Kosuke Namba、Keiko Shimamoto、Tetsuro Shinada

  DOI：10.1016/s0040-4039(03)01316-9

  日期：2003.7

  Efficient synthesis of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740: 1) and its structurally related analogs (-)-2 and (-)-3 has been accomplished starting with (1S,2R)-1-amino-2-hydroxycyclopentane- or cyclohexanecarboxylic acid (4 or 17) via an intramolecular cyclopropanation of alpha-diazo acetamide. (C) 2003 Elsevier Science Ltd. All rights reserved.