1-iodo-4-(2-iodoethoxy)benzene | 67856-41-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-iodo-4-(2-iodoethoxy)benzene
• CAS: 67856-41-1
• 化学式: C₈H₈I₂O
• 分子量: 373.96
• InChiKey: UDIAAXMDYGRKAP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-iodo-4-(2-iodoethoxy)benzene 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 sodium hydride 、 sodium carbonate 作用下， 以 乙醇 、 水 、 N,N-二甲基甲酰胺 、 甲苯 、 mineral oil 为溶剂， 反应 0.75h， 生成 (6S)-2-nitro-6-(2-{4-[6-trifluoromethyl-3-pyridinyl]phenoxy}ethoxy)-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine
  参考文献：
  名称：

  Synthesis and Structure–Activity Relationships of Varied Ether Linker Analogues of the Antitubercular Drug (6S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)

  摘要：

  New analogues of antitubercular drug PA-824 were synthesized, featuring alternative side chain ether linkers of varying size and flexibility, seeking drug candidates with enhanced metabolic stability and high efficacy. Both alpha-methyl substitution and removal of the benzylic methylene were broadly tolerated in vitro, with a biaryl example of the latter class exhibiting an 8-fold better efficacy than the parent drug in a mouse model of acute Mycobacterium tuberculosis infection and negligible fragmentation to an alcohol metabolite in liver microsomes. Extended linkers (notably propenyloxy, propynyloxy, and pentynyloxy) provided greater potencies against replicating M. tb (monoaryl analogues), with propynyl ethers being most effective under anaerobic (nonreplicating) conditions (mono/biaryl analogues). For benzyloxybenzyl and biaryl derivatives, aerobic activity was maximal with the original (OCH2) linker. One propynyloxy-linked compound displayed an 89-fold higher efficacy than the parent drug in the acute model, and it was slightly superior to antitubercular drug OPC-67683 in a chronic infection model.

  DOI：

  10.1021/jm200377r
• 作为产物：
  描述：

  2-(4-碘-苯氧基)-乙醇 在 咪唑 、 碘 、 三苯基膦 作用下， 以 二氯甲烷 为溶剂， 反应 19.0h， 以97%的产率得到1-iodo-4-(2-iodoethoxy)benzene
  参考文献：
  名称：

  Synthesis and Structure–Activity Relationships of Varied Ether Linker Analogues of the Antitubercular Drug (6S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)

  摘要：

  New analogues of antitubercular drug PA-824 were synthesized, featuring alternative side chain ether linkers of varying size and flexibility, seeking drug candidates with enhanced metabolic stability and high efficacy. Both alpha-methyl substitution and removal of the benzylic methylene were broadly tolerated in vitro, with a biaryl example of the latter class exhibiting an 8-fold better efficacy than the parent drug in a mouse model of acute Mycobacterium tuberculosis infection and negligible fragmentation to an alcohol metabolite in liver microsomes. Extended linkers (notably propenyloxy, propynyloxy, and pentynyloxy) provided greater potencies against replicating M. tb (monoaryl analogues), with propynyl ethers being most effective under anaerobic (nonreplicating) conditions (mono/biaryl analogues). For benzyloxybenzyl and biaryl derivatives, aerobic activity was maximal with the original (OCH2) linker. One propynyloxy-linked compound displayed an 89-fold higher efficacy than the parent drug in the acute model, and it was slightly superior to antitubercular drug OPC-67683 in a chronic infection model.

  DOI：

  10.1021/jm200377r

文献信息

• <i>N</i>-Haloimide-enabled halogenation <i>via</i> halogen-bond-assisted C–C activation of alkanols
  作者：Yan Geng、Yue Ma、Rui Huang、Xingwei Li、Songjie Yu

  DOI：10.1039/d2gc03768h

  日期：——

  halogen-bond-assisted C–C activation of cyclic and acyclic alkanols in the absence of catalysts and oxidants, where the inexpensive N-haloimides act as bifunctional reagents to activate and halogenate alcohols. This redox-neutral protocol is a general method for the halogenation of the C–C bonds of primary, secondary, and tertiary alkanols, thus installing three types of halogen atoms and boronic esters

  醇基原料惰性 C-C 键的选择性卤化在合成化学中具有重要意义。以前的卤化反应通常需要金属催化剂和/或氧化剂，并且仅限于裂解叔环烷醇的 C-C 键。在此，我们报告了一种广泛适用的合成碘代烷烃、溴代烷烃和氯代烷烃的策略，在没有催化剂和氧化剂的情况下，通过卤键辅助的环烷醇和无环烷醇的 C-C 活化，其中廉价的N-卤代酰亚胺作为双功能试剂激活和卤化醇。这种氧化还原中性方案是卤化伯、仲和叔烷醇的 C-C 键的通用方法，从而通过一锅脱碘-硼酸酯化在各种原料中安装三种类型的卤素原子和硼酸酯以实用和可持续的方式生产化学品。
• PYRIDONE AMIDES AS MODULATORS OF SODIUM CHANNELS
  申请人：Vertex Pharmaceuticals Incorporated

  公开号：EP3239134A1

  公开（公告）日：2017-11-01

  The invention relates to pyridone amide compounds of formula I and I'or pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels: The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders, including pain.

  本发明涉及式 I 和 I'的吡啶酮酰胺化合物或其药学上可接受的盐类，可用作钠通道抑制剂： 本发明还提供了包含本发明化合物的药学上可接受的组合物，以及使用该组合物治疗包括疼痛在内的各种疾病的方法。
• GOOSEN A.; MCCLELAND C. W., J. CHEM. SOC. PERKIN TRANS., PART 1, 1978, NO 6, 646-652
  作者：GOOSEN A.、 MCCLELAND C. W.

  DOI：——

  日期：——