4-Fluor-N-methylphthalimid | 63196-44-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: 4-Fluor-N-methylphthalimid
• 英文别名: 4-fluoro-N-methylphthalimide；5-fluoro-2-methyl-isoindole-1,3-dione；5-Fluoro-2-methylisoindole-1,3-dione
• CAS: 63196-44-1
• 化学式: C₉H₆FNO₂
• 分子量: 179.151
• InChiKey: DPYPKRLYESDBOK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  37.4
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF ANDROGEN RECEPTOR
  申请人：Arvinas, Inc.

  公开号：US20180099940A1

  公开（公告）日：2018-04-12

  The present disclosure relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.

  本公开涉及双功能化合物，其用于降解和（抑制）雄激素受体。具体而言，本公开涉及包含一端结合到E3泛素连接酶的谷氨酰腺苷环配体，另一端结合到雄激素受体的部分的化合物，使得雄激素受体与泛素连接酶靠近，以实现雄激素受体的降解（和抑制）。本公开展示了与根据本公开涉及的化合物相关的广泛的药理活性范围，与雄激素受体的降解/抑制一致。
• [EN] BENZOXAZINONE DERIVATIVES USEFUL AS HERBICIDES<br/>[FR] DÉRIVÉS DE BENZOXAZINONE UTILES EN TANT QU'HERBICIDES
  申请人：REDAG CROP PROT LTD

  公开号：WO2019020987A1

  公开（公告）日：2019-01-31

  The present invention relates to compounds which are of use in the field of agriculture as herbicides. The compounds in question are of formula II and comprise a spirofused tricycle core: wherein R4 and R5 together with the carbon atom to which they are attached form a cyclic group.

  本发明涉及一种在农业领域作为除草剂使用的化合物。所涉及的化合物属于公式II，并包括一个螺合三环核心：其中R4和R5与它们附着的碳原子一起形成一个环状基团。
• NEW PHENYLALANINE DERIVATIVES
  申请人：SUZUKI Nobuyasu

  公开号：US20090048236A1

  公开（公告）日：2009-02-19

  Specific phenylalanine derivatives or pharmaceutically acceptable salts thereof have an antagonistic effect on the α4 integrins and, therefore, are usable as therapeutic agents or preventive agents for diseases in which α4 integrin-depending adhesion process participates in the pathology, such as inflammatory diseases, rheumatoid arthritis, inflammatory bowel diseases, systemic lupus erythematosus, multiple sclerosis, Sjögren's syndrome, asthma, psoriasis, allergy, diabetes, cardiovascular diseases, arterial sclerosis, restenosis, tumor proliferation, tumor metastasis and transplantation rejection.

  特定的苯丙氨酸衍生物或其药学上可接受的盐具有对α4整合素的拮抗作用，因此可用作治疗剂或预防剂，用于α4整合素依赖性黏附过程参与病理的疾病，如炎症性疾病、类风湿性关节炎、炎症性肠病、系统性红斑狼疮、多发性硬化症、干燥综合症、哮喘、银屑病、过敏、糖尿病、心血管疾病、动脉硬化、再狭窄、肿瘤增殖、肿瘤转移和移植排斥。
• Method for making aromatic etherimides
  申请人：GENERAL ELECTRIC COMPANY

  公开号：EP0119576A1

  公开（公告）日：1984-09-26

  A method for making aromatic ether imides is provided by effecting the displacement of reactive radicals on a phthalimide nucleus with a mono- or bis-alkali metal phenoxide in the presence of a nonpolar solvent and a phase transfer catalyst, such as a triorganoborate. The aromatic ether imide made by the present invention are useful intermediates for making aromatic ether anhydrides and aromatic bis (ether anhydrides).

  本发明提供了一种制造芳香族醚酰亚胺的方法，即在非极性溶剂和相转移催化剂（如三机硼酸盐）存在下，用一碱金属或双碱金属酚氧化物对邻苯二甲酰亚胺核上的活性自由基进行置换。本发明制得的芳香族醚酰亚胺是制造芳香族醚酐和芳香族双（醚酐）的有用中间体。
• Phase transfer catalysts
  申请人：GENERAL ELECTRIC COMPANY

  公开号：EP0126951A2

  公开（公告）日：1984-12-05

  Branched alkyldiorganoaminopyridinium salts have been found useful as phase transfer catalysts for facilitating nucleophilic aromatic substitution. For example, the 2-ethylhexyl salts of dialkylaminopyridine, can be used as stable phase transfer catalysts for making aromatic etherimides by reacting substituted phthalimides and alkali metal phenoxides in the presence of a non-polar organic solvent.

  人们发现支链烷基低甘油氨基吡啶鎓盐可用作相转移催化剂，促进亲核芳香取代反应。例如，二烷基氨基吡啶的 2-乙基己基盐可用作稳定的相转移催化剂，在非极性有机溶剂存在下，使取代的邻苯二甲酰亚胺和碱金属苯氧基化物发生反应，生成芳香族醚酰亚胺。