(E)-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-1-methylindolin-2-one | 56680-35-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: (E)-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-1-methylindolin-2-one
• 英文别名: 3-[(E)-2-(4-methoxy-phenyl)-2-oxo-ethylidene]-1-methyl-1,3-dihydro-indol-2-one；(3E)-3-[2-(4-methoxyphenyl)-2-oxoethylidene]-1-methylindol-2-one
• CAS: 56680-35-4
• 化学式: C₁₈H₁₅NO₃
• 分子量: 293.322
• InChiKey: KVWZHPHNFHDHQM-RVDMUPIBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (E)-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-1-methylindolin-2-one 在 4-二甲氨基吡啶 、 Ir(dFppy)₃ 、 叠氮基三甲基硅烷 、 水 作用下， 以 乙腈 为溶剂， 以62 %的产率得到
  参考文献：
  名称：

  通过光催化脱氮进行骨骼重排：获得 C-3 氨基喹啉-2(1H)-酮

  摘要：

  将胺基添加到杂芳族系统中是一项具有挑战性的合成过程，但它是许多生物活性分子开发中必不可少的过程。在这里，我们报告了一种合成 3-氨基喹啉-2(1 H )-one 的替代方法，该方法通过级联 C-N 键形成和脱氮过程编辑分子骨架，克服了传统方法的局限性。我们使用 TMSN 3作为胺化剂，并使用多种 3-亚叉吲哚作为 quinolin-2(1 H )-one 主链的合成前体，这对敏感官能团具有显着的耐受性。对照实验表明三唑啉中间体在产物的形成中起重要作用。光谱研究进一步确定了潜在的反应途径。

  DOI：

  10.1039/d3sc04447e
• 作为产物：
  描述：

  3-hydroxy-3-(2-(4-methoxyphenyl)-2-oxoethyl)-1-methylindolin-2-one 在 盐酸 、 溶剂黄146 作用下， 以 乙醇 为溶剂， 反应 16.0h， 生成 (E)-3-(2-(4-methoxyphenyl)-2-oxoethylidene)-1-methylindolin-2-one
  参考文献：
  名称：

  Studies on the stereochemical assignment of 3-acylidene 2-oxindoles

  摘要：

  通过NMR光谱对3-酰基吲哚类化合物中E/Z几何异构体的命名可能会导致不正确的烯烃立体化学分配，因为在一系列大类类似物中观察到的化学位移范围较窄。相较之下，UV-Vis光谱为烯烃立体化学分配提供了一种方便且更可靠的方法。X射线晶体学与理论研究的结合表明，UV-Vis光谱行为的观察差异与Z-异构体的扭曲构象有关，该构象相对于E-异构体提供了降低的共轭效应和较弱的紫外光移吸收。

  DOI：

  10.1039/c4ob00496e

文献信息

• An easy lewis acid-mediated isomerization from (E)- to (Z)-Oxoindolin-3-ylidene ketones.
  作者：Giuseppe Faita、Mariella Mella、PierPaolo Righetti、Gianfranco Tacconi

  DOI：10.1016/s0040-4020(01)85706-9

  日期：1994.1

  (E)-2-Oxoindolin-3-ylidene ketones can be easily isomerized to their (Z)-isomers by AlCl3 at room temperature in CH2Cl2. The behaviour of the unsaturated dicarbonyl framework in the (Z)-configuration as a bidentate ligand can be the key-step of the isomerization. The limits of a reaction that allows to prepare several yet-unknown products is discussed.

  在室温下，CH 2 Cl 2中的AlCl 3可以很容易地将（E）-2-氧代吲哚-3-亚基酮异构化为（Z）异构体。（Z）-构型中作为二齿配体的不饱和二羰基骨架的行为可能是异构化的关键步骤。讨论了可以制备几种尚不知道的产物的反应极限。
• Difluorocarbene-Enabled Synthesis of 3-Alkenyl-2-oxindoles from <i>ortho</i>-Aminophenylacetylenes
  作者：Shanglin Chen、Hua Huang、Xin Li、Xingxing Ma、Jianke Su、Qiuling Song

  DOI：10.1021/acs.orglett.3c00150

  日期：2023.2.24

  cyclization pathway from difluorocarbene and ortho-amino aryl alkynone, rendering an effective and universal strategy for the construction of 3-alkenyl-2-oxindoles. Our strategy starts from cheap and accessible ortho-amino aryl alkynone instead of the direct indole skeleton; moreover, in situ generated difluorocarbene from commercially available halogenated difluoroalkylative reagents enables the cleavage

  在此，我们报道了一种来自二氟卡宾和邻氨基芳基炔酮的无过渡金属 [4 + 1] 环化途径，为构建 3-烯基-2-羟吲哚提供了一种有效且通用的策略。我们的策略从廉价易得的邻氨基芳基炔酮开始，而不是直接的吲哚骨架；此外，从市售的卤化二氟烷基化试剂中原位生成的二氟卡宾能够裂解 C-N 键并形成新的 C-N 键和 C-C 键。
• Synthesis and biological evaluation of spiro[cyclopropane-1,3′-indolin]-2′-ones as potential anticancer agents
  作者：Chada Narsimha Reddy、V. Lakshma Nayak、Geeta Sai Mani、Jeevak Sopanrao Kapure、Praveen Reddy Adiyala、Ram Awatar Maurya、Ahmed Kamal

  DOI：10.1016/j.bmcl.2015.08.056

  日期：2015.10

  Libraries of spiro[cyclopropane-1,3'-indolin]-2'-ones were synthesized and evaluated for their biological activity against five different human cancer cell lines HT-29 (colon cancer), DU-145 (prostate cancer), Hela (cervical cancer), A-549 (Lung cancer), and MCF-7 (breast cancer). Many compounds of the series exhibited promising anticancer activity (IC50 < 20 mu M) against the studied cell lines. Based on the screening results, a structure activity relationship (SAR) of the pharmacophore was proposed. Among the series compound 6b and 6u showed significant activity against human prostate cancer cell line, DU-145. Flow cytometric analysis showed that these two compounds arrested the cell cycle in the G0/G1 phase leading to caspase-3 dependent apoptotic cell death. Further, measurement of mitochondrial membrane potential and Annexin V-FITC assay also suggested that 6b and 6u induced cell death by apoptosis. (C) 2015 Elsevier Ltd. All rights reserved.
• Phosphine-Catalyzed Asymmetric [4+2] Annulation of Vinyl Ketones with Oxindole-Derived α,β-Unsaturated Imines: Enantioselective Syntheses of 2′,3′-Dihydro-1′<i>H</i>-spiro[indoline-3,4′-pyridin]-2-ones
  作者：Xiao-Nan Zhang、Gen-Qiang Chen、Xiang Dong、Yin Wei、Min Shi

  DOI：10.1002/adsc.201300828

  日期：2013.11.25

  AbstractA novel asymmetric [4+2] annulation of vinyl ketones with oxindole‐derived α,β‐unsaturated imines has been developed in the presence of a multifunctional thiourea‐phosphine catalyst derived from a natural amino acid, providing the first phosphine‐catalyzed enantioselective synthesis of 2′,3′‐dihydro‐1′H‐spiro[indoline‐3,4′‐pyridin]‐2‐ones in good yields with excellent stereoselectivities under mild conditions.magnified image
• Reaction of 2-Oxoindolin-3-Ylidene Derivatives with Heterocyclic Enamines. A Convenient One-Pot Synthesis of Pyrimido [5,4:5',6']Pyrido[2,3-b]-Indole-2,4-Dione and Spiro Indolin-2-One-3,5'-Pyrido [2,3-d] Pyrimidines
  作者：Abdel-Aziz S. El-ahl

  DOI：10.1080/00397910008087401

  日期：2000.1

  The reaction of 6-aminouracils 2a, b with 2-oxoindolin-3-ylideneacetophenones la-h afforded Pyrimido[5,4:5', 6'] pyrido-[2, 3-b] indole- 2, 4-diones 3 a-k via a regiospecific Michael addition, followed by cyclization, Alternatively, the reaction of 2a with 2-oxoindolin-3-ylidenemalononitriles 6a, b gave rise to regiospecific formation of spiro indolin-2-one-3, 5'-pyrido[2,3-d]pyrimidines 7a,b.