(2'S)-4-(2'-tert-butoxycarbonylamino-3'-hydroxypropyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid di-tert-butyl ester | 596828-14-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: (2'S)-4-(2'-tert-butoxycarbonylamino-3'-hydroxypropyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid di-tert-butyl ester
• 英文别名: ditert-butyl 4-[(2S)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
• CAS: 596828-14-7
• 化学式: C₂₅H₄₂N₂O₇
• 分子量: 482.618
• InChiKey: WFWOLVUNOJVFTP-INIZCTEOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  34
• 可旋转键数：
  12
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.72
• 拓扑面积：
  123
• 氢给体数：
  3
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  (2'S)-4-(2'-tert-butoxycarbonylamino-3'-hydroxypropyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid di-tert-butyl ester 在 jones reagent 、 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 生成 (2'S,1''S)-4-[2'-tert-butoxycarbonylamino-2'-(1''-methoxycarbonyl-2''phenylethylcarbamoyl)ethyl]-2,6-dimethylpyridine-3,5-dicarboxylic acid di-tert-butyl ester
  参考文献：
  名称：

  Model Studies toward the Synthesis of Dihydropyrimidinyl and Pyridyl α-Amino Acids via Three-Component Biginelli and Hantzsch Cyclocondensations

  摘要：

  A novel and versatile strategy for the synthesis of heterocyclic a-amino acids has been described. The use of components (aldehyde or beta-ketoester) bearing a masked glycinyl moiety in Biginelli and Hantzsch cyclocondensations allowed access to the 4-dihydropyrimidinyl-alpha-glycines, 4-dihydropyrimidinyl-alpha-alanines, 4-pyridyl-alpha-alanines, and 2-pyridyl-alpha-alanines classes. Dihydropyrimidinyl-amino acids were obtained as a mixture of diastereoisomers due to the formation of the stereocenter at C4 of the dibydropyrimidinone ring. Individual stereoisomers were isolated as pure compounds and their structures were assigned with the aid of X-ray crystallography and chiroptical properties. The enantiomeric purity of a representative selection of the above amino acids was greater than 96% as verified by derivatization to the corresponding Mosher's amides and subsequent H-1 and F-19 NMR spectroscopy. Incorporation of the 4-pyridyl-alpha-alanine derivative into a peptide chain is also described.

  DOI：

  10.1021/jo0342830
• 作为产物：
  描述：

  2,2-二甲基-4-(2-氧代乙基)?唑啉-3-羧酸-(S)-叔丁酯 在 4 A molecular sieve 、 水 、 溶剂黄146 作用下， 以 叔丁醇 为溶剂， 反应 48.0h， 生成 (2'S)-4-(2'-tert-butoxycarbonylamino-3'-hydroxypropyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid di-tert-butyl ester
  参考文献：
  名称：

  Model Studies toward the Synthesis of Dihydropyrimidinyl and Pyridyl α-Amino Acids via Three-Component Biginelli and Hantzsch Cyclocondensations

  摘要：

  A novel and versatile strategy for the synthesis of heterocyclic a-amino acids has been described. The use of components (aldehyde or beta-ketoester) bearing a masked glycinyl moiety in Biginelli and Hantzsch cyclocondensations allowed access to the 4-dihydropyrimidinyl-alpha-glycines, 4-dihydropyrimidinyl-alpha-alanines, 4-pyridyl-alpha-alanines, and 2-pyridyl-alpha-alanines classes. Dihydropyrimidinyl-amino acids were obtained as a mixture of diastereoisomers due to the formation of the stereocenter at C4 of the dibydropyrimidinone ring. Individual stereoisomers were isolated as pure compounds and their structures were assigned with the aid of X-ray crystallography and chiroptical properties. The enantiomeric purity of a representative selection of the above amino acids was greater than 96% as verified by derivatization to the corresponding Mosher's amides and subsequent H-1 and F-19 NMR spectroscopy. Incorporation of the 4-pyridyl-alpha-alanine derivative into a peptide chain is also described.

  DOI：

  10.1021/jo0342830

文献信息

• Model Studies toward the Synthesis of Dihydropyrimidinyl and Pyridyl α-Amino Acids via Three-Component Biginelli and Hantzsch Cyclocondensations
  作者：Alessandro Dondoni、Alessandro Massi、Erik Minghini、Simona Sabbatini、Valerio Bertolasi

  DOI：10.1021/jo0342830

  日期：2003.8.1

  A novel and versatile strategy for the synthesis of heterocyclic a-amino acids has been described. The use of components (aldehyde or beta-ketoester) bearing a masked glycinyl moiety in Biginelli and Hantzsch cyclocondensations allowed access to the 4-dihydropyrimidinyl-alpha-glycines, 4-dihydropyrimidinyl-alpha-alanines, 4-pyridyl-alpha-alanines, and 2-pyridyl-alpha-alanines classes. Dihydropyrimidinyl-amino acids were obtained as a mixture of diastereoisomers due to the formation of the stereocenter at C4 of the dibydropyrimidinone ring. Individual stereoisomers were isolated as pure compounds and their structures were assigned with the aid of X-ray crystallography and chiroptical properties. The enantiomeric purity of a representative selection of the above amino acids was greater than 96% as verified by derivatization to the corresponding Mosher's amides and subsequent H-1 and F-19 NMR spectroscopy. Incorporation of the 4-pyridyl-alpha-alanine derivative into a peptide chain is also described.