2-溴甲基-3-羟基吡啶 | 82414-44-6

• 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
• 中文名称: 2-溴甲基-3-羟基吡啶
• 英文名称: 2-bromomethyl-3-hydroxypyridine
• 英文别名: 2-(bromomethyl)-3-pyridinol；2-(Bromomethyl)pyridin-3-ol
• CAS: 82414-44-6
• 化学式: C₆H₆BrNO
• 分子量: 188.024
• InChiKey: UBGCCLCUBAMUMA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  9
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  33.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-溴甲基-3-羟基吡啶 在 platinum(IV) oxide 氢气 、 三乙胺 作用下， 以 1,4-二氧六环 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.5h， 生成 (5R,6R)-6-ethyl-3-[(3-hydroxypyridin-2-yl)methylsulfanyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
  参考文献：
  名称：

  Versatile chemical modification of lthe C-2 side chain of carbapenem antibiotics

  摘要：

  DOI：

  10.1016/s0040-4039(00)86977-4
• 作为产物：
  描述：

  3-羟基-2-羟甲基吡啶盐酸盐 、 碳酸氢钠 在 氢溴酸 、 溶剂黄146 作用下， 以 二氯甲烷 、 水 为溶剂， 生成 2-溴甲基-3-羟基吡啶
  参考文献：
  名称：

  Method for labelling phosphorylated peptides, complex compounds used in the methods, process for producing the same, and their intermediates

  摘要：

  公开号：

  EP1455189B1

文献信息

• [EN] HETEROAROMATIC ELECTROPHILES AND METHODS OF USING THEREOF<br/>[FR] ÉLECTROPHILES HÉTÉROAROMATIQUES ET LEURS PROCÉDÉS D'UTILISATION
  申请人：OHIO STATE INNOVATION FOUNDATION

  公开号：WO2018152329A1

  公开（公告）日：2018-08-23

  Disclosed herein are compounds, compositions, and methods for reactivating or realkylating aged acetylcholinesterase inhibited by or conjugated to the organophosphorus compound. The organophosphorus compound can be a nerve agent. The acetylcholinesterase can be in the central nerve system (CNS) and/or the peripheral nervous system (PNS) of a subject. Accordingly, methods for ameliorating, diminishing, reversing, treating or preventing the toxic effects of an organophosphorus compound in a subject are provided herein. Methods for prophylactic or therapeutic treatment of exposure to an organophosphorus nerve agent are also provided.

  本文揭示了一种化合物、组合物和方法，用于重新激活或重新烷基化被有机磷化合物抑制或结合的老化乙酰胆碱酯酶。有机磷化合物可以是神经毒剂。乙酰胆碱酯酶可以存在于受试者的中枢神经系统（CNS）和/或外周神经系统（PNS）。因此，本文提供了用于改善、减轻、逆转、治疗或预防受试者中有机磷化合物毒性影响的方法。还提供了用于预防或治疗暴露于有机磷神经毒剂的方法。
• 3 -AMINO- PYRAZOLE DERIVATIVES USEFUL AGAINST TUBERCULOSIS
  申请人：Castro Pichel Julia

  公开号：US20130203802A1

  公开（公告）日：2013-08-08

  A compound of Formula (I) or a pharmaceutically acceptable salt thereof: Wherein: Het is a 5 to 10-membered heteroaromatic ring; Either X is N and Y is CR 5 ; or X is C and Y is S; Z is selected from N and CH; R 1 is selected from H and C 1-2 alkyl; R 2 is selected from H, C 1-2 alkyl, OH, —CH 2 OH and C 1-2 alkoxy; Each R 3 is independently selected from OH, C 1-3 alkyl, F, Cl, Br, NH 2 , and C 1-3 alkoxy; R 4 is selected from C 1-3 alkyl and haloC 1-3 alkyl; R 5 is selected from H, C 1-3 alkyl and haloC 1-3 alkyl; R 6 and R 7 are either i) each independently selected from H, C 1-3 alkyl and C 1-3 alkoxy; or ii) R 6 and R 7 together with the ring to which they are attached form a 9-membered bicyclic ring; p is 0-3; and R A is selected from H and C 1-3 alkyl, compositions containing them, their use in therapy, for example in the treatment of tuberculosis, and methods for the preparation of such compounds, are provided.

  公式（I）的化合物或其药用盐：其中：Het是5至10成员的杂环芳香环；X为N且Y为CR5；或X为C且Y为S；Z从N和CH中选择；R1从H和C1-2烷基中选择；R2从H、C1-2烷基、OH、—CH2OH和C1-2烷氧基中选择；每个R3独立选择自OH、C1-3烷基、F、Cl、Br、NH2和C1-3烷氧基；R4从C1-3烷基和卤代C1-3烷基中选择；R5从H、C1-3烷基和卤代C1-3烷基中选择；R6和R7要么i）各自独立选择自H、C1-3烷基和C1-3烷氧基；要么ii）R6和R7与它们附着的环一起形成9成员双环环；p为0-3；RA从H和C1-3烷基中选择，提供了含有它们的组合物，它们在治疗中的使用，例如在结核病的治疗中，并提供了这类化合物的制备方法。
• [EN] 3 -AMINO- PYRAZOLE DERIVATIVES USEFUL AGAINST TUBERCULOSIS<br/>[FR] DÉRIVÉS DE 3-AMINO-PYRAZOLE UTILES CONTRE LA TUBERCULOSE
  申请人：GLAXO GROUP LTD

  公开号：WO2012049161A1

  公开（公告）日：2012-04-19

  A compound of Formula (I) or a pharmaceutically acceptable salt thereof: (I), Wherein: Het is a 5 to 10-membered heteroaromatic ring; Either X is N and Y is CR5; or X is C and Y is S; Z is selected from N and CH; R1 is selected from H and C1-2alkyl; R2 is selected from H, C1-2alkyl, OH, -CH2OH and C1-2alkoxy; Each R3 is independently selected from OH, C1-3alkyl, F, Cl, Br, NH2, and C1-3alkoxy; R4 is selected from C1-3alkyl and haloC1-3alkyl; R5 is selected from H, C1-3alkyl and haloC1-3alkyl; R6 and R7 are either i) each independently selected from H, C1-3alkyl and C1-3alkoxy; or ii) R6 and R7 together with the ring to which they are attached form a 9-membered bicylic ring; p is 0-3; and RA is selected from H and C1-3alkyl, compositions containing them, their use in therapy, for example in the treatment of tuberculosis, and methods for the preparation of such compounds, are provided.

  化合物的化学式（I）或其药学上可接受的盐：（I），其中：Het是一个5到10个成员的杂芳环；X是N且Y是CR5；或X是C且Y是S；Z从N和CH中选择；R1从H和C1-2烷基中选择；R2从H，C1-2烷基，OH，-CH2OH和C1-2烷氧基中选择；每个R3独立地从OH，C1-3烷基，F，Cl，Br，NH2和C1-3烷氧基中选择；R4从C1-3烷基和卤代C1-3烷基中选择；R5从H，C1-3烷基和卤代C1-3烷基中选择；R6和R7要么i）各自独立地从H，C1-3烷基和C1-3烷氧基中选择；要么ii）R6和R7与它们附着的环一起形成一个9个成员的双环环；p为0-3；RA从H和C1-3烷基中选择，提供了含有它们的组合物，它们在治疗中的用途，例如在结核病治疗中的用途，以及这类化合物的制备方法。
• Method for labeling phosphorylated peptides, method for selectively adsorbing phosphorylated peptides, complex compounds used in the methods, process for producing the complex compounds, and raw material compounds for the complex compounds
  申请人：Kabushiki Kaisha Nard Kenkyusho

  公开号：US20040198712A1

  公开（公告）日：2004-10-07

  Provided are a method for easily detecting phosphorylated peptides, namely, proteins, in samples derived from living organisms or the like, a method for selectively adsorbing the phosphorylated peptides, and compounds that are highly coordinated to the phosphorylated peptides and usable in the methods. The complex compound is represented by the formula: 1 wherein X is a linker moiety, and Y is a labeling group. The compound (I) is highly coordinated to a phosphorylated peptide, and has a labeling group. Accordingly, with use of the compound (I), the phosphorylated peptide can be easily identified.

  提供了一种易于检测活体生物等样本中的磷酸化肽（即蛋白质）的方法，一种选择性吸附磷酸化肽的方法，以及可用于这些方法的高度配合到磷酸化肽的化合物。该复合物化合物由式1表示：其中X是连接基团，Y是标记基团。化合物（I）与磷酸化肽高度配合，并具有标记基团。因此，使用化合物（I），可以轻松识别磷酸化肽。
• 3-amino-pyrazole derivatives useful against tuberculosis
  申请人：Castro Pichel Julia

  公开号：US08779153B2

  公开（公告）日：2014-07-15

  A compound of Formula (I) or a pharmaceutically acceptable salt thereof: Wherein: Het is a 5 to 10-membered heteroaromatic ring; Either X is N and Y is CR5; or X is C and Y is S; Z is selected from N and CH; R1 is selected from H and C1-2alkyl; R2 is selected from H, C1-2alkyl, OH, —CH2OH and C1-2alkoxy; Each R3 is independently selected from OH, C1-3alkyl, F, Cl, Br, NH2, and C1-3alkoxy; R4 is selected from C1-3alkyl and haloC1-3alkyl; R5 is selected from H, C1-3alkyl and haloC1-3alkyl; R6 and R7 are either i) each independently selected from H, C1-3alkyl and C1-3alkoxy; or ii) R6 and R7 together with the ring to which they are attached form a 9-membered bicylic ring; p is 0-3; and RA is selected from H and C1-3alkyl, compositions containing them, their use in therapy, for example in the treatment of tuberculosis, and methods for the preparation of such compounds, are provided.

  化合物的式子（I）或其药学上可接受的盐： 其中：Het是5至10个成员的杂环芳香环；X为N且Y为CR5，或者X为C且Y为S；Z从N和CH中选择；R1从H和C1-2烷基中选择；R2从H，C1-2烷基，OH，—CH2OH和C1-2烷氧基中选择；每个R3独立地从OH，C1-3烷基，F，Cl，Br，NH2和C1-3烷氧基中选择；R4从C1-3烷基和haloC1-3烷基中选择；R5从H，C1-3烷基和haloC1-3烷基中选择；R6和R7要么各自独立地从H，C1-3烷基和C1-3烷氧基中选择；要么R6和R7与它们附着的环一起形成一个9成员的双环；p为0-3；RA从H和C1-3烷基中选择，提供了含有它们的组成物，它们在治疗中的使用，例如在结核病的治疗中，以及这种化合物的制备方法。