4-cyanoindan | 15115-63-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚满类
• 英文名称: 4-cyanoindan
• 英文别名: 4-Cyan-indan；2,3-Dihydro-1H-indene-4-carbonitrile
• CAS: 15115-63-6
• 化学式: C₁₀H₉N
• 分子量: 143.188
• InChiKey: NTLQZJLDVPCONP-UHFFFAOYSA-N

物化性质

• 沸点：
  270.3±29.0 °C(Predicted)
• 密度：
  1.10±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  23.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  4-cyanoindan 在 lithium aluminium tetrahydride 、 potassium carbonate 、 sodium hydroxide 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 1.0h， 生成 (E)-N-((2,3-dihydro-1H-inden-4-yl)methyl)-N-methyl-3-phenylprop-2-en-1-amine
  参考文献：
  名称：

  Discovery of Benzocycloalkane Derivatives Efficiently Blocking Bacterial Virulence for the Treatment of Methicillin-Resistant S. aureus (MRSA) Infections by Targeting Diapophytoene Desaturase (CrtN)

  摘要：

  Antivirulence strategies are now attracting interest for the inherent mechanism of action advantages. In our previous work, diapophytoene desaturase (CrtN) was identified to be an attractive and drugable target for fighting pigmented S. aureus infections. In this research, we developed a series of effective benzocycloalkane-derived CrtN inhibitors with submicromolar IC50. Analogue 8 blocked the pigment biosynthesis of three MRSA strains with a nanomolar IC50 value. Corresponding to its mode of action, 8 did not function as a bactericidal agent. 8 could sensitize S. aureus to immune clearance. In vivo, 8 was proven to be efficacious in an S. aureus Newman sepsis model and abscess formation model. For two typical MRSAs,. USA400 MW2 and Mu50, 8 significantly decreased the staphylococcal loads in the liver and kidneys. Moreover, 8 showed minimal antifungal activity compared to that of NTF. In summary, 8 has the potential to be developed as a therapeutic drug, especially against intractable MRSA issues.

  DOI：

  10.1021/acs.jmedchem.6b00122
• 作为产物：
  描述：

  4-氯-1-茚满酮 在 喹啉 、 盐酸 、 汞 、 锌 作用下， 生成 4-cyanoindan
  参考文献：
  名称：

  Faller,P., Bulletin de la Societe Chimique de France, 1966, p. 3618 - 3625

  摘要：

  DOI：

文献信息

• Pyrethrinoid esters carrying an indanyl nucleus and their use as
  申请人：Roussel Uclaf

  公开号：US05180741A1

  公开（公告）日：1993-01-19

  Pyrenthrinoid esters with an indenyl nucleus having the following structural formula ##STR1## wherein the substituents are herein defined, have been shown to be useful as pesticides and in pesticidal compositions.

  具有以下结构公式的茚满基核的拟除虫菊酯酯类，其中取代基在本发明中定义，已被证明作为杀虫剂以及在杀虫剂组合物中是有用的。
• Dual Ligand-Enabled Nondirected C–H Cyanation of Arenes
  作者：Hao Chen、Arup Mondal、Philipp Wedi、Manuel van Gemmeren

  DOI：10.1021/acscatal.8b04639

  日期：2019.3.1

  structural units in organic chemistry and, therefore, highly attractive targets for C–H activation. Herein, the development of an arene-limited, nondirected C–H cyanation based on the use of two cooperatively acting commercially available ligands is reported. The reaction enables the cyanation of arenes by C–H activation in the absence of directing groups and is therefore complementary to established

  芳香腈是有机化学中的关键结构单元，因此是C–H活化的极具吸引力的目标。在此，据报道，基于使用两种可协同作用的市售配体，开发了一种受芳烃限制的，无方向性的CH氰基氰化反应。该反应可在没有导向基团的情况下通过C–H活化使芳烃氰化，因此可与已建立的方法互补。
• [EN] PROCESS FOR THE PREPARATION OF SPHINGOSINE-1-PHOSPHATE RECEPTOR AGONIST<br/>[FR] PROCÉDÉ DE PRÉPARATION D'UN AGONISTE DU RÉCEPTEUR DE LA SPHINGOSINE-1-PHOSPHATE
  申请人：QUIM SINTETICA S A

  公开号：WO2020064818A1

  公开（公告）日：2020-04-02

  Industrially viable and advantageous processes for the preparation of Ozanimod are described. The invention also discloses the intermediates obtained in the process.

  描述了用于制备奥扎尼莫德的工业可行且有利的工艺。该发明还披露了在该过程中获得的中间体。
• [EN] COMPOUNDS AND METHODS FOR TREATING LUPUS<br/>[FR] COMPOSÉS ET MÉTHODES POUR LE TRAITEMENT DE L'INFLAMMATION
  申请人：CELGENE INT II SARL

  公开号：WO2018064356A1

  公开（公告）日：2018-04-05

  Methods for treatment of systemic lupus erythematosus (SLE" or "Lupus") by administration of a modulator of sphingosine-1-phosphate receptor subtype 1 (S1P1), as well as compositions and methods related to the same, wherein such S1P1 modulators have the following general structure and wherein X and Y are as defined herein.

  通过给予鞘氨醇-1-磷酸受体亚型1（S1P1）调节剂治疗全身性红斑狼疮（SLE或“狼疮”的方法，以及与之相关的组合物和方法，其中这些S1P1调节剂具有以下一般结构，其中X和Y如下所定义。
• [EN] INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL<br/>[FR] INHIBITEURS DU CANAL POTASSIQUE MÉDULLAIRE EXTÉRIEUR RÉNAL
  申请人：MERCK SHARP & DOHME

  公开号：WO2013062892A1

  公开（公告）日：2013-05-02

  The present invention provides compounds of Formula (I) and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir 1.1) channel. The compounds act as diuretics and natriuretics and are valuable pharmaceutically active compounds for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension and conditions resulting from excessive salt and water retention.

  本发明提供了式（I）的化合物及其药学上可接受的盐，这些化合物是ROMK（Kir 1.1）通道的抑制剂。这些化合物作为利尿剂和钠利尿剂，并且是治疗和预防包括高血压和由过多盐和水潴留引起的疾病等医学状况的有价值的药用活性化合物。