phosphonooxymethyl 4-((1R,4R,5R)-5-amino-2-azabicyclo[2.2.1]heptan-2-yl)-6-fluoro-2-(2-methylpyrimidin-5-yloxy)-9H-pyrimido[4,5-b]indol-8-yl(methyl)carbamate | 1581682-59-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: phosphonooxymethyl 4-((1R,4R,5R)-5-amino-2-azabicyclo[2.2.1]heptan-2-yl)-6-fluoro-2-(2-methylpyrimidin-5-yloxy)-9H-pyrimido[4,5-b]indol-8-yl(methyl)carbamate
• 英文别名: phosphonooxymethyl N-[4-[(1R,4R,5R)-5-amino-2-azabicyclo[2.2.1]heptan-2-yl]-6-fluoro-2-(2-methylpyrimidin-5-yl)oxy-9H-pyrimido[4,5-b]indol-8-yl]-N-methylcarbamate
• CAS: 1581682-59-8
• 化学式: C₂₄H₂₆FN₈O₇P
• 分子量: 588.492
• InChiKey: DEEHQAQZAOFRQR-SUYBPPKGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.4
• 重原子数：
  41
• 可旋转键数：
  8
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  202
• 氢给体数：
  4
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  chloromethyl 4-((1R,4R,5R)-5-Boc-amino-2-azabicyclo[2.2.1]heptan-2-yl)-6-fluoro-2-(2-methylpyrimidin-5-yloxy)-9H-pyrimido[4,5-b]indol-8-yl(methyl)carbamate 在 三氟乙酸 、 sodium iodide 作用下， 以 四氢呋喃 为溶剂， 反应 3.25h， 生成 phosphonooxymethyl 4-((1R,4R,5R)-5-amino-2-azabicyclo[2.2.1]heptan-2-yl)-6-fluoro-2-(2-methylpyrimidin-5-yloxy)-9H-pyrimido[4,5-b]indol-8-yl(methyl)carbamate
  参考文献：
  名称：

  [EN] TRICYCLIC GYRASE INHIBITORS FOR USE AS ANTIBACTERIAL AGENTS
  [FR] INHIBITEURS TRICYCLIQUES DE GYRASE UTILISABLES COMME AGENTS ANTIBACTÉRIENS

  摘要：

  本文披露了具有化学式I结构的化合物及其药用盐、酯和前药，这些化合物可用作抗菌有效的三环酶抑制剂。此外，本文还披露了三环酶抑制剂化合物的种属。还考虑了相关的药用组合物、用途和制备这些化合物的方法。

  公开号：

  WO2014043272A1

文献信息

• TRICYCLIC GYRASE INHIBITORS
  申请人：TRIUS THERAPEUTICS INC.

  公开号：US20150246934A1

  公开（公告）日：2015-09-03

  Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. In addition, species of tricyclic gyrase inhibitors compounds are also disclosed herein. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

  本文揭示了具有I式结构的化合物及其药物适宜的盐、酯和前药，它们可用作具有抗菌作用的三环酶抑制剂。此外，本文还揭示了三环酶抑制剂化合物的种类。还考虑了相关的制药组合物、用途和制备化合物的方法。
• Tricyclic Gyrase inhibitors
  申请人：MERCK SHARP & DOHME CORP.

  公开号：US10865216B2

  公开（公告）日：2020-12-15

  Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. In addition, species of tricyclic gyrase inhibitors compounds are also disclosed herein. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

  本文公开了具有式 I 结构的化合物及其药学上适用的盐、酯和原药，它们可作为抗菌有效的三环回旋酶抑制剂。此外，本文还公开了三环回旋酶抑制剂化合物的种类。 还考虑了相关的药物组合物、用途和化合物的制造方法。
• [EN] TRICYCLIC GYRASE INHIBITORS FOR USE AS ANTIBACTERIAL AGENTS<br/>[FR] INHIBITEURS TRICYCLIQUES DE GYRASE UTILISABLES COMME AGENTS ANTIBACTÉRIENS
  申请人：TRIUS THERAPEUTICS INC

  公开号：WO2014043272A1

  公开（公告）日：2014-03-20

  Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. In addition, species of tricyclic gyrase inhibitors compounds are also disclosed herein. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

  本文披露了具有化学式I结构的化合物及其药用盐、酯和前药，这些化合物可用作抗菌有效的三环酶抑制剂。此外，本文还披露了三环酶抑制剂化合物的种属。还考虑了相关的药用组合物、用途和制备这些化合物的方法。