tert-butyl (1S,2R)-3-azido-1-benzyl-2-hydroxypropylcarbamate | 162536-72-3

• 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: tert-butyl (1S,2R)-3-azido-1-benzyl-2-hydroxypropylcarbamate
• 英文别名: [R-(R*,S*)]-[3-Azido-2-hydroxy-1-(phenylmethyl) propyl]carbamic acid, 1,1-dimethylethyl ester；((1S,2R)-3-azido-1-benzyl-2-hydroxy-propyl)carbamic acid t-butyl ester；((1S,2R)-3-azido-1-benzyl-2-hydroxy-propyl)-carbamic acid tert-butyl ester；(1S,2R)-(3-azido-1-benzyl-2-hydroxy-propyl)-carbamic acid t-butyl ester；tert-butyl N-[(2S,3R)-4-azido-3-hydroxy-1-phenylbutan-2-yl]carbamate
• CAS: 162536-72-3
• 化学式: C₁₅H₂₂N₄O₃
• 分子量: 306.365
• InChiKey: LECORZARFQSVSF-QWHCGFSZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  22
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  72.9
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  tert-butyl (1S,2R)-3-azido-1-benzyl-2-hydroxypropylcarbamate 在 palladium on activated charcoal 4-二甲氨基吡啶 、 氢气 、 三乙酰氧基硼氢化钠 、 溶剂黄146 、 N,N-二异丙基乙胺 、 三氟乙酸 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 二甲基亚砜 、 乙腈 为溶剂， 60.0 ℃ 、275.79 kPa 条件下， 生成 {(1S,2R)-3-[(Benzo[1,3]dioxole-5-sulfonyl)-(6-cyano-2,2-dimethyl-hexyl)-amino]-1-benzyl-2-hydroxy-propyl}-carbamic acid (3R,3aS,6aR)-(hexahydro-furo[2,3-b]furan-3-yl) ester
  参考文献：
  名称：

  Novel arylsulfonamides possessing sub-picomolar HIV protease activities and potent anti-HIV activity against wild-type and drug-resistant viral strains

  摘要：

  A novel series of P1' chain-extended arylsufonamides was synthesiszed and evaluated for wild-type HIV protease inhibitory activity and in vitro antiviral activity against wild type virus and two protease inhibitor-resistant mutant viruses. All of the compounds showed dramatic increases in enzyme activity as compared to the currently marketed HIV protease inhibitors amprenavir, indinavir, and nelfinavir. In addition, significant improvements in antiviral potencies against wild type and the two mutant viruses were also realized. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.008
• 作为产物：
  描述：

  1-苄基-2,3-环氧正丙基-氨基甲酸叔丁酯 在 sodium azide 、 氯化铵 作用下， 以 甲醇 为溶剂， 反应 16.0h， 以90%的产率得到tert-butyl (1S,2R)-3-azido-1-benzyl-2-hydroxypropylcarbamate
  参考文献：
  名称：

  [EN] NOVEL SULFONE AMIDE DERIVATIVES CAPABLE OF INHIBITING BACE
  [FR] NOUVEAUX DERIVES SULFONAMIDE CAPABLES D'INHIBER BACE

  摘要：

  本发明涉及本公开中定义的式1的磺酰脒衍生物，该衍生物抑制BACE（或β-分泌酶）的活性。这些磺酰脒衍生物可用于治疗和预防由β-淀粉样蛋白产生引起的阿尔茨海默病及相关疾病，通过抑制BACE的活性。

  公开号：

  WO2005030709A1

文献信息

• [EN] 4-ARYL-BUTANE-1,3-DIAMIDES<br/>[FR] 4-ARYLBUTANE-1,3-DIAMIDES
  申请人：NOVARTIS AG

  公开号：WO2010086366A1

  公开（公告）日：2010-08-05

  The invention relates to compound of the formula (I) in which the substituents are as defined in the specification; m free form or in salt form; to its preparation, to its use as medicament and to medicaments comprising it.

  这项发明涉及式(I)的化合物，其中取代基如规范中定义；m自由形式或盐形式；其制备，作为药物的用途以及包含它的药物。
• HIV protease inhibiting compounds
  申请人：Flentge A. Charles

  公开号：US20050131042A1

  公开（公告）日：2005-06-16

  A compound of the formula is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

  披露了一种公式的化合物作为HIV蛋白酶抑制剂。还披露了用于抑制HIV感染的方法和组合物。
• [EN] NOVEL SULFONE AMIDE DERIVATIVES CAPABLE OF INHIBITING BACE<br/>[FR] NOUVEAUX DERIVES SULFONAMIDE CAPABLES D'INHIBER BACE
  申请人：LG LIFE SCIENCES LTD

  公开号：WO2005030709A1

  公开（公告）日：2005-04-07

  The present invention relates to novel derivatives of sulfone amide of Formula 1 as defined in this disclosure which inhibit the activity of BACE (or beta-secretase). These sulfone amide derivatives are useful for the treatment and prevention of Alzheimer's disease and related diseases caused by production of beta-amyloid, by inhibiting the activity of BACE.

  本发明涉及本公开中定义的式1的磺酰脒衍生物，该衍生物抑制BACE（或β-分泌酶）的活性。这些磺酰脒衍生物可用于治疗和预防由β-淀粉样蛋白产生引起的阿尔茨海默病及相关疾病，通过抑制BACE的活性。
• Retrocarbamate protease inhibitors
  申请人：Bristol-Myers Squibb Co.

  公开号：US05492910A1

  公开（公告）日：1996-02-20

  The invention discloses compounds of the formula ##STR1## are disclosed as HIV protease inhibitors.

  该发明揭示了公式##STR1##的化合物作为HIV蛋白酶抑制剂。
• INDOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS
  申请人：Kim Soon Ha

  公开号：US20100210647A1

  公开（公告）日：2010-08-19

  The present invention relates to new indole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole compounds as an active ingredient.

  本发明涉及新的吲哚化合物，其药学上可接受的盐或异构体，用于预防或治疗细胞坏死和坏死相关疾病。本发明还涉及一种预防或治疗细胞坏死和坏死相关疾病的方法和组合物，该组合物包括所述吲哚化合物作为活性成分。