3-溴-6-羟基-2-甲基苯甲醛 | 137644-94-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 3-溴-6-羟基-2-甲基苯甲醛
• 英文名称: 3-bromo-6-hydroxy-2-methylbenzaldehyde
• CAS: 137644-94-1
• 化学式: C₈H₇BrO₂
• 分子量: 215.046
• InChiKey: GYSFTNVHSLJTCO-UHFFFAOYSA-N

物化性质

• 沸点：
  268.1±35.0 °C(Predicted)
• 密度：
  1.629±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2913000090
• 储存条件：
  2-8°C

反应信息

• 作为反应物：
  描述：

  3-溴-6-羟基-2-甲基苯甲醛 在 platinum(IV) oxide 草酰氯 、 氢气 、 四氯化锡 、 镍 、 三氟乙酸 作用下， 以 乙醚 、 二氯甲烷 、 苯 为溶剂， 反应 19.25h， 生成 2-<3-(4-diazo-3-oxobutyl)-2-methoxy-4-methylphenyl>acetic acid ethyl ester
  参考文献：
  名称：

  Pseudoguaianolides from intramolecular cycloadditions of aryl diazoketones: synthesis of (±)-confertin and an approach to the synthesis of (±)-damsin

  摘要：

  Rhodium(II) mandelate-catalysed cyclisation of alpha-diazoketones derived from 3-arylpropionic acids produces bicyclo[5.3.0]decatrienones, one of which has been used to synthesise an advanced (+/-)-confertin intermediate in six stages and 20% overall yield. The possibility of constructing intermediates for the synthesis of damsin-like pseudoguaianolides via catalysed diazoketone cyclisation is also examined and methods for the construction of polyfunctional 3-arylpropionic acids suitable for use as damsin precursors are presented.

  DOI：

  10.1039/p19910002565
• 作为产物：
  描述：

  2-甲氧基-6-甲基苯甲醛 在 溴 、 三溴化硼 、 铁粉 作用下， 以 四氯化碳 、 二氯甲烷 为溶剂， 反应 4.0h， 生成 3-溴-6-羟基-2-甲基苯甲醛
  参考文献：
  名称：

  FXR受体激动剂

  摘要：

  本发明公开了一种FXR受体激动剂。本发明属于医药技术领域，具体涉及式(I)所示的化合物、其药学上可接受的盐、其酯或其立体异构体，R1、R2、R3、M、L、L1、W、A、B、Q、m、n如说明书中所定义；本发明还涉及这些化合物的制备方法、药物制剂及在用于制备治疗和/或预防由FXR受体介导的非酒精性脂肪肝、原发性胆汁性肝硬化、脂质代谢紊乱、糖尿病并发症及恶性肿瘤等相关疾病的药物中的应用。

  公开号：

  CN109265471B

文献信息

• Benzofurane, benzothiophene, benzothiazol derivatives as FXR modulators
  申请人：Merck Sante

  公开号：EP2110374A1

  公开（公告）日：2009-10-21

  The present invention relates to compounds of formula (I) wherein the substituents are as defined in the claims, including pharmaceutical compositions thereof and for their use in the treatment and/or prevention and/or amelioration of one or more symptoms of disease or disorders related to the activity of FXR. The invention is also directed to intermediates and to a method of preparation of compounds of formula (I).

  本发明涉及式(I)的化合物，其中取代基如权利要求中定义的那样，包括其药物组合物及其用于治疗和/或预防及/或改善与FXR活性相关的疾病或障碍的一个或多个症状。本发明还涉及中间体以及化合物式(I)的制备方法。
• BENZOFURANE, BENZOTHIOPHENE, BENZOTHIAZOL DERIVATIVES AS FXR MODULATORS
  申请人：Roche Didier

  公开号：US20110105475A1

  公开（公告）日：2011-05-05

  The present invention relates to compounds of formula (I) wherein the substituents are as defined in the claims, including pharmaceutical compositions thereof and for their use in the treatment and/or prevention and/or amelioration of one or more symptoms of disease or disorders related to the activity of FXR. The invention is also directed to intermediates and to a method of preparation of compounds of formula (I).

  本发明涉及公式（I）化合物，其中取代基如权利要求中所定义，包括其药物组合物以及用于治疗和/或预防和/或改善与FXR活性相关的一种或多种疾病或障碍的症状的用途。本发明还涉及中间体以及制备公式（I）化合物的方法。
• BICYCLIC COMPOUND
  申请人：Kamata Makoto

  公开号：US20120010247A1

  公开（公告）日：2012-01-12

  The present invention provides a compound having an ACC inhibitory action, which is useful as an agent for the prophylaxis or treatment of obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia, cancer and the like, and has superior efficacy. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.

  本发明提供了一种具有ACC抑制作用的化合物，其可用作预防或治疗肥胖症、糖尿病、高血压、高脂血症、心衰、糖尿病并发症、代谢综合征、肌肉萎缩、癌症等的药物，并具有优越的疗效。本发明涉及一种由式(I)表示的化合物，其中每个符号如规范中所定义，或其盐。
• [EN] BORON CONTAINING PYRAZOLE COMPOUNDS, COMPOSITIONS COMPRISING THEM, METHODS AND USES THEREOF<br/>[FR] COMPOSÉS PYRAZOLE CONTENANT DU BORE, COMPOSITIONS COMPRENANT CEUX-CI, MÉTHODES ET UTILISATIONS ASSOCIÉES
  申请人：BOEHRINGER INGELHEIM ANIMAL HEALTH USA INC

  公开号：WO2022133420A1

  公开（公告）日：2022-06-23

  The present invention describes novel boron containing pyrazole compounds, or their pharmaceutically acceptable salts, pharmaceutical compositions containing them, and their medical uses. The compounds of the invention have activity as Janus kinase (JAK) inhibitors and are useful in the treatment or control of inflammation, auto-immune diseases, cancer, and other disorders and indications where modulation of JAK would be desirable. Also described are methods of treating inflammation, auto-immune diseases, cancer, and other conditions that are susceptible to the inhibition of a Janus kinase by administering a compound herein described.

  本发明描述了新型含硼吡唑化合物或其药学上可接受的盐、包含它们的制药组合物以及它们的医学用途。本发明化合物具有作为Janus激酶（JAK）抑制剂的活性，并且在治疗或控制炎症、自身免疫性疾病、癌症和其他需要调节JAK的疾病和适应症中有用。还描述了通过给予本文所述化合物来抑制Janus激酶以治疗炎症、自身免疫性疾病、癌症和其他易受抑制Janus激酶的疾病和症状的方法。
• BENZOFURANE DERIVATIVES AS FXR MODULATORS
  申请人：Merck Patent GmbH

  公开号：EP2262785B1

  公开（公告）日：2015-01-14