5-异丙氧基-2-甲基苯胺 | 918445-10-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 中文名称: 5-异丙氧基-2-甲基苯胺
• 英文名称: 5-isopropoxy-2-methylbenzenamine
• 英文别名: 5-Isopropoxy-2-methylaniline；2-methyl-5-propan-2-yloxyaniline
• CAS: 918445-10-0
• 化学式: C₁₀H₁₅NO
• 分子量: 165.235
• InChiKey: ZWCXUSBRKRTYFL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  35.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5-异丙氧基-2-甲基苯胺 在 N-溴代丁二酰亚胺(NBS) 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 4-Bromo-5-isopropoxy-2-methylaniline
  参考文献：
  名称：

  Discovery, Optimization, and Biological Evaluation of 5-(2-(Trifluoromethyl)phenyl)indazoles as a Novel Class of Transient Receptor Potential A1 (TRPA1) Antagonists

  摘要：

  A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagonist of the transient receptor potential A1 (TRPA1) ion channel with IC50 = 1.23 μM. Hit to lead medicinal chemistry optimization established the SAR around the indazole ring system, demonstrating that a trifluoromethyl group at the 2-position of the phenyl ring in combination with various substituents at the 6-position of the indazole ring greatly contributed to improvements in vitro activity. Further lead optimization resulted in the identification of compound 31, a potent and selective antagonist of TRPA1 in vitro (IC50 = 0.015 μM), which has moderate oral bioavailability in rodents and demonstrates robust activity in vivo in several rodent models of inflammatory pain.

  DOI：

  10.1021/jm401986p
• 作为产物：
  描述：

  4-甲基-3-硝基苯酚 在 palladium on activated charcoal 、 甲酸铵 、 potassium carbonate 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 生成 5-异丙氧基-2-甲基苯胺
  参考文献：
  名称：

  Discovery, Optimization, and Biological Evaluation of 5-(2-(Trifluoromethyl)phenyl)indazoles as a Novel Class of Transient Receptor Potential A1 (TRPA1) Antagonists

  摘要：

  A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagonist of the transient receptor potential A1 (TRPA1) ion channel with IC50 = 1.23 μM. Hit to lead medicinal chemistry optimization established the SAR around the indazole ring system, demonstrating that a trifluoromethyl group at the 2-position of the phenyl ring in combination with various substituents at the 6-position of the indazole ring greatly contributed to improvements in vitro activity. Further lead optimization resulted in the identification of compound 31, a potent and selective antagonist of TRPA1 in vitro (IC50 = 0.015 μM), which has moderate oral bioavailability in rodents and demonstrates robust activity in vivo in several rodent models of inflammatory pain.

  DOI：

  10.1021/jm401986p

文献信息

• [EN] INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE<br/>[FR] INHIBITEURS DE TYROSINE KINASE DE BRUTON ET LEURS PROCÉDÉS D'UTILISATION
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2018103058A1

  公开（公告）日：2018-06-14

  Compounds of formula (I') and methods of their use and preparation, as well as compositions comprising compounds of formula (I').

  公式（I'）的化合物及其使用和制备方法，以及包含公式（I'）化合物的组合物。
• [EN] AMINOTRIAZOLES FOR THE TREATMENT OF DEMYELINATING DISEASES<br/>[FR] AMINOTRIAZOLES POUR TRAITER DES MALADIES DÉMYÉLINISANTES
  申请人：VERTEX PHARMA

  公开号：WO2018106646A1

  公开（公告）日：2018-06-14

  The invention relates to triazole compounds of formula (I') or pharmaceutically acceptable salts thereof, useful as modulators of demyelinating diseases: wherein A is selected from the group consisting of (i), (ii), (iii), (iv), (v), and (vi) The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention, methods of using the compositions and kits thereof in the treatment of various demyelinating and neurodegenerative diseases, including multiple sclerosis.

  该发明涉及式(I')的三唑化合物或其药学上可接受的盐，用作脱髓鞘疾病的调节剂：其中A选自(i)、(ii)、(iii)、(iv)、(v)和(vi)所述的组。该发明还提供包括该发明化合物的药学上可接受的组合物，以及在治疗各种脱髓鞘和神经退行性疾病，包括多发性硬化症中使用这些组合物和配套工具的方法。
• KNOWN AND NEW HETEROCYCLIC COMPOUNDS AS PEST CONTROL AGENTS
  申请人：BAYER CROPSCIENCE AKTIENGESELLSCHAFT

  公开号：US20160106102A1

  公开（公告）日：2016-04-21

  The present application relates to the use of known and novel heterocyclic compounds for controlling animal pests, to novel heterocyclic compounds, to processes for preparation thereof and to the use thereof for controlling animal pests.

  本申请涉及使用已知和新型杂环化合物来控制动物害虫，涉及新型杂环化合物，其制备方法以及用于控制动物害虫的使用方法。
• Heterocyclic Non-Peptide GNRH Antagonists
  申请人：Showell Graham Andrew

  公开号：US20090209522A1

  公开（公告）日：2009-08-20

  A compound of formula (I): wherein either B is absent and A and Z are the same or different and are each hydrogen, halogen, alkyl, hydroxy, alkoxy, —CN, —C(R c ) 2 OH, —N(R d )C(═X)R c , —C(═X)N(R c )(R d ), —S(O) m —R c , —N(R c )(R d )S(O) 2 , —S(O) 2 N(R c )(R d ), —N(R c ) 2 , aryl optionally substituted with R a or —O-aryl optionally substituted with R a ; or B is present and is —(CH 2 ) n —, —C(R b ) 2 — or —O—, or B taken together with A or Z can be —C═C(R b )—, —C(R b )═C—, —CH 2 —CH(R b )— or —CH(R b )—CH 2 —; D is —O— or —S(O) m′ —; E is a bond or is —(CH 2 ) n —, —N(R d )—, —(CH 2 ) n N(R d )— or —N(R d )(CH 2 ) n —; F is —C(═X)—; G is —(CH 2 ) n —, —N(R d )—, —(CH 2 ) n N(R d )— or —N(R d )(CH 2 ) n ; J is a bond, —O—, —N(R C )C(═X)—, —C(═X)N(R c )—, —S(O) m′ —, —N(R c )S(O) m —, —S(O) n N(R c )—, —N(R c )— or —N(R g )(R h ); K is a bond, alkylene, cycloalkylene, cycloalkenylene, arylene, heterocycloalkylene, heterocycloalkylene or heteroarylene; and L is hydrogen or a terminal group; has therapeutic utility.

  化合物的化学式（I）：其中B可能不存在，而A和Z相同或不同，分别为氢、卤素、烷基、羟基、烷氧基、—CN、—C（Rc）2OH、—N（Rd）C（═X）Rc、—C（═X）N（Rc）（Rd）、—S（O）m—Rc、—N（Rc）（Rd）S（O）2、—S（O）2N（Rc）（Rd）、—N（Rc）2、取代为Ra的芳基或—O-取代为Ra的芳基；或B存在且为—（CH2）n—、—C（Rb）2—或—O—，或B与A或Z一起可以是—C═C（Rb）—、—C（Rb）═C—、—CH2—CH（Rb）—或—CH（Rb）—CH2—；D为—O—或—S（O）m′—；E为键或—（CH2）n—、—N（Rd）—、—（CH2）nN（Rd）—或—N（Rd）（CH2）n—；F为—C（═X）—；G为—（CH2）n—、—N（Rd）—、—（CH2）nN（Rd）—或—N（Rd）（CH2）n；J为键、—O—、—N（RC）C（═X）—、—C（═X）N（Rc）—、—S（O）m′—、—N（Rc）S（O）m—、—S（O）nN（Rc）—、—N（Rc）—或—N（Rg）（Rh）；K为键、烷基、环烷基、环烯基、芳基、杂环烷基、杂环烷基或杂芳基；L为氢或端基；具有治疗效用。
• Cytotoxic peptides and conjugates thereof
  申请人：NOVARTIS AG

  公开号：US10392421B2

  公开（公告）日：2019-08-27

  Disclosed herein are novel cytotoxic peptides of formula (I) as described herein: and the use of such peptides in making immunoconjugates (i.e Antibody Drug Conjugates) Also described herein are immunoconjugates (i.e Antibody Drug Conjugates) comprising such novel cytotoxic peptide linked to an antigen binding moiety, such as an antibody; where such immunoconjugates are useful for treating cell proliferative disorders. The invention further provides pharmaceutical compositions comprising these immunoconjugates, compositions comprising the immunoconjugates with a therapeutic co-agent, and methods to use these immunoconjugates and compositions for treating cell proliferation disorders.

  本文公开了如本文所述的式 (I) 的新型细胞毒性肽： 以及使用这种肽制造免疫结合剂（即抗体药物结合剂）的方法 本发明还描述了免疫结合剂（即抗体药物结合剂），其包含与抗原结合分子（如抗体）连接的这种新型细胞毒性肽；其中这种免疫结合剂可用于治疗细胞增殖性疾病。本发明进一步提供了包含这些免疫共轭物的药物组合物、包含这些免疫共轭物与治疗共用试剂的组合物，以及使用这些免疫共轭物和组合物治疗细胞增殖障碍的方法。