2-(2,3-dioxoindolin-1-yl)acetyl chloride | 19612-82-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2-(2,3-dioxoindolin-1-yl)acetyl chloride
• 英文别名: (2,3-dioxo-indolin-1-yl)-acetyl chloride；1-chlorocarbonylmethyl-1H-indole-2,3-dione；2-(2,3-Dioxoindol-1-yl)acetyl chloride
• CAS: 19612-82-9
• 化学式: C₁₀H₆ClNO₃
• 分子量: 223.616
• InChiKey: IDYPGMHPJOOAKW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  54.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(2,3-dioxoindolin-1-yl)acetyl chloride 在 溴 、 溶剂黄146 作用下， 生成 ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)acetate
  参考文献：
  名称：

  Steinkopf; Hempel, Justus Liebigs Annalen der Chemie, 1932, vol. 495, p. 144,162

  摘要：

  DOI：
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 氯化亚砜 作用下， 生成 2-(2,3-dioxoindolin-1-yl)acetyl chloride
  参考文献：
  名称：

  Langenbeck, Chemische Berichte, 1928, vol. 61, p. 944

  摘要：

  DOI：

文献信息

• Isatine derivatives, their preparation and use
  申请人：NEUROSEARCH A/S

  公开号：EP0432648A2

  公开（公告）日：1991-06-19

  A method of treatment with compounds having the formula wherein R¹ is hydrogen, C₁₋₆-alkyl which may be branched, C₃₋₇-cycloalkyl, benzyl, phenyl which may be substituted, acyl, hydroxy, C₁₋₆-alkoxy, CH₂CO₂R' wherein R' is hydrogen or C₁₋₆-alkyl which may be branched, CH₂CN, CH₂CONRIVRV wherein RIV and RV independently are hydrogen or C₁₋₆-alkyl, or CH₂C(=NOH)NH₂; R² is hydrogen, benzyl, C₁₋₆-alkyl which may be branched, or C₃₋₇-cycloalkyl; R⁴, R⁵, R⁶, R⁷ independently are hydrogen, C₁₋₆-alkyl which may be branched, phenyl, halogen, C₁₋₆-alkoxy, NO₂, CN, SO₂NR''R''' wherein R'' and R''' independently are hydrogen or C₁₋₆-alkyl, or CF₃; or R⁶ and R⁷ together form an additional 4 to 7 membered ring which may be aromatic or partial saturated and which may be substituted with halogen, NO₂, CF₃, CN, SO₂NR''R''' wherein R'' and R''' independently are hydrogen or C₁₋₆-alkyl, and R⁴ and R⁵ have the meanings set forth above, are disclosed, as well as pharmaceutical compositions thereof. Certain of the compounds are novel. The compounds and pharmaceutical compositions containing the compounds are useful in the treatment of central nervous system disorders and especially conditions sensitive to excitatory amino acids.

  一种用具有以下式子的化合物进行处理的方法 其中 R¹ 是氢、C₁₋₆-烷基（可以是支链）、C₃₋₇-环烷基、苄基、苯基（可以是取代的）、酰基、羟基、C₁₋₆-烷氧基、CH₂CO₂R'，其中 R' 为氢或 C₁₋₆- 烷基（可为支链）、CH₂CN、CH₂CONRIVRV，其中 RIV 和 RV 独立地为氢或 C₁₋₆- 烷基，或 CH₂C(=NOH)NH₂； R² 是氢、苄基、C₁₋₆-烷基（可以是支链）或 C₃₋₇-环烷基； R⁴、R⁵、R⁶、R⁷各自为氢、C₁₋₆-烷基（可为支链）、苯基、卤素、C₁₋₆-烷氧基、NO₂、CN、SO₂NR''R'''（其中 R'' 和 R''' 各自为氢或 C₁₋₆-烷基）或 CF₃；或 R⁶ 和 R⁷ 共同形成另外一个 4 至 7 个成员的环，该环可以是芳香族或部分饱和环，可以被卤素、NO₂、CF₃、CN、公开了 SO₂NR''R'''，其中 R'' 和 R''' 独立地为氢或 C₁₋₆ 烷基，且 R⁴ 和 R⁵ 具有上述含义，还公开了其药物组合物。其中某些化合物是新颖的。 这些化合物和含有这些化合物的药物组合物可用于治疗中枢神经系统疾病，特别是对兴奋性氨基酸敏感的疾病。
• X-ray crystallographic study of diversely substituted isatin derivatives
  作者：E.V. Mironova、A.V. Bogdanov、D.B. Krivolapov、L.I. Musin、I.A. Litvinov、V.F. Mironov

  DOI：10.1016/j.molstruc.2014.09.021

  日期：2015.1

  A series of isatin derivatives were synthesized and studied by XRD. For the first time the peculiarities of the molecule structure and crystal packing effects were analyzed. Indoline heterocycles are planar in all the investigated structures. The molecules bearing the sterically hindered substituents at nitrogen atom of indoline heterocycle have the maximum deviations of two oxygen atoms from the indoline plane. The substituent nature at nitrogen atom does not effect on the bond lengths of indoline moiety. The value of endocyclic bond angle at nitrogen not so strongly depends on the substituent and is almost equal to the one in unsubstituted isatin. In contrast to the unsubstituted isatin, where the system of classical hydrogen N-H center dot center dot center dot O-bonds is realized, in crystals of investigated compounds there is no opportunity to reveal ones, and the crystal structure is stabilized by C-H center dot center dot center dot O- and pi-pi-interactions. (C) 2014 Elsevier B.V. All rights reserved.
• Discovery of novel non-peptide inhibitors of BACE-1 using virtual high-throughput screening
  作者：N. Yi Mok、James Chadwick、Katherine A.B. Kellett、Nigel M. Hooper、A. Peter Johnson、Colin W.G. Fishwick

  DOI：10.1016/j.bmcl.2009.09.103

  日期：2009.12

  A novel series of isatin-based inhibitors of beta-secretase (BACE-1) have been identified using a virtual high-throughput screening approach. Structure-activity relationship studies revealed structural features important for inhibition. Docking studies suggest these inhibitors may bind within the BACE-1 active site through H-bonding interactions involving the catalytic aspartate residues. (C) 2009 Elsevier Ltd. All rights reserved.
• Respiratory syncytial virus fusion inhibitors. Part 7: Structure–activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo
  作者：Ny Sin、Brian L. Venables、Keith D. Combrink、H. Belgin Gulgeze、Kuo-Long Yu、Rita L. Civiello、Jan Thuring、X. Alan Wang、Zheng Yang、Lisa Zadjura、Anthony Marino、Kathleen F. Kadow、Christopher W. Cianci、Junius Clarke、Eugene V. Genovesi、Ivette Medina、Lucinda Lamb、Mark Krystal、Nicholas A. Meanwell

  DOI：10.1016/j.bmcl.2009.06.030

  日期：2009.8

  A series of bezimidazole-isatin oximes were prepared and profiled as inhibitors of respiratory syncytial virus (RSV) replication in cell culture. Structure-activity relationship studies were directed toward optimization of antiviral activity, cell permeability and metabolic stability in human liver micorosomes (HLM). Parallel combinatorial synthetic chemistry was employed to functionalize isatin oximes via O-alkylation which quickly identified a subset of small, lipophilic substituents that established good potency for the series. Further optimization of the isatin oxime derivatives focused on introduction of nitrogen atoms to the isatin phenyl ring to provide a series of aza-isatin oximes with significantly improved PK properties. Several aza-isatin oximes analogs displayed targeted metabolic stability in HLM and permeability across a confluent monolayer of CaCo-2 cells. These studies identified several compounds, including 18i, 18j and 18n that demonstrated antiviral activity in the BALB/c mouse model of RSV infection following oral dosing. (C) 2009 Elsevier Ltd. All rights reserved.
• Langenbeck, Chemische Berichte, 1928, vol. 61, p. 944
  作者：Langenbeck

  DOI：——

  日期：——