(p-iodoanilido)ferrocene carboxylic acid | 254112-34-0

• 英文名称: (p-iodoanilido)ferrocene carboxylic acid
• CAS: 254112-34-0
• 化学式: C₁₇H₁₄FeINO
• 分子量: 431.056
• InChiKey: LEARCPDBKYAWMC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为反应物：
  描述：

  tert-butyl N-[(2S)-1-(3-ethylpent-1-yn-3-ylamino)-4-methylsulfanyl-1-oxobutan-2-yl]carbamate 、 (p-iodoanilido)ferrocene carboxylic acid 在 PdCl₂(PPh₃)2 、 CuI 、 Et₃N 作用下， 以 四氢呋喃 、 三乙胺 为溶剂， 生成
  参考文献：
  名称：

  Synthesis of Alkynyl Amino Acids and Peptides and Their Palladium-Catalyzed Coupling to Ferrocene

  摘要：

  A method for attaching organometallics to the C-terminus of amino acids via a Pd-catalyzed two-step procedure is presented. Boc-protected enantiomerically pure amino acids 1 (a Phe, b Leu, c Met, d Ser) are reacted with 1,1-diethylpropargylamine to yield alkynyl amino acids 2. After reaction with (p-iodoanilido)ferrocene carboxylic acid 3 in the presence of 5 mol % PdCl2(PPh3)(2)/CuI ferrocene amino acids 4 are obtained in ca. 80% yield. The reaction does not require anhydrous conditions and tolerates functional groups such as amides, alcohols (Ser, 4d) or thioethers (Met, 4c). A complete characterization by multinuclear NMR (including N-15) is carried out. Cyclic voltammetry shows a reversible wave at about +190 mV (vs Fc/Fc(+)) independent of the nature of the attached amino acid. In the solid state, 2a forms a left-handed helix along the crystallographic c axis which is stabilized by hydrogen bonds as revealed by a single-crystal X-ray structure determination. A comparison of IR data in solution and the solid slate suggests that hydrogen bonding is also important for the solid-state structures of ferrocene amino acids 4 but does not play a role in solution. The use of this methodology for peptide chemistry is demonstrated by labeling the dipeptide Boc-Met-Phe-OH at the C-terminus and the tripeptide Boc-Phe-Glu-Leu-OMe with ferrocene. The alkyne anchoring group in the tripeptide is introduced at the Cy(Glu) atom at an early stage of the peptide synthesis and is not affected by subsequent deprotection and coupling reactions.

  DOI：

  10.1021/ic990256+
• 作为产物：
  描述：

  二茂铁甲酸 、 对碘苯胺 在 oxalic acid 、 CH₂Cl₂ 、 Et₃N 作用下， 以 二氯甲烷 为溶剂， 以90%的产率得到(p-iodoanilido)ferrocene carboxylic acid
  参考文献：
  名称：

  Synthesis of Alkynyl Amino Acids and Peptides and Their Palladium-Catalyzed Coupling to Ferrocene

  摘要：

  A method for attaching organometallics to the C-terminus of amino acids via a Pd-catalyzed two-step procedure is presented. Boc-protected enantiomerically pure amino acids 1 (a Phe, b Leu, c Met, d Ser) are reacted with 1,1-diethylpropargylamine to yield alkynyl amino acids 2. After reaction with (p-iodoanilido)ferrocene carboxylic acid 3 in the presence of 5 mol % PdCl2(PPh3)(2)/CuI ferrocene amino acids 4 are obtained in ca. 80% yield. The reaction does not require anhydrous conditions and tolerates functional groups such as amides, alcohols (Ser, 4d) or thioethers (Met, 4c). A complete characterization by multinuclear NMR (including N-15) is carried out. Cyclic voltammetry shows a reversible wave at about +190 mV (vs Fc/Fc(+)) independent of the nature of the attached amino acid. In the solid state, 2a forms a left-handed helix along the crystallographic c axis which is stabilized by hydrogen bonds as revealed by a single-crystal X-ray structure determination. A comparison of IR data in solution and the solid slate suggests that hydrogen bonding is also important for the solid-state structures of ferrocene amino acids 4 but does not play a role in solution. The use of this methodology for peptide chemistry is demonstrated by labeling the dipeptide Boc-Met-Phe-OH at the C-terminus and the tripeptide Boc-Phe-Glu-Leu-OMe with ferrocene. The alkyne anchoring group in the tripeptide is introduced at the Cy(Glu) atom at an early stage of the peptide synthesis and is not affected by subsequent deprotection and coupling reactions.

  DOI：

  10.1021/ic990256+