2,2-dimethylpentanedioyl dichloride | 133003-98-2

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 酰卤
• 英文名称: 2,2-dimethylpentanedioyl dichloride
• 英文别名: 2,2-dimethyl-pentanedioyl chloride；2,2-Dimethyl-glutarylchlorid
• CAS: 133003-98-2
• 化学式: C₇H₁₀Cl₂O₂
• mdl: MFCD11617046
• 分子量: 197.061
• InChiKey: WBKXOLKOAFPWRR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  11
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.714
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2,2-dimethylpentanedioyl dichloride 在 palladium on activated charcoal lithium aluminium tetrahydride 、 氢气 作用下， 以 四氢呋喃 、 甲醇 、 乙二醇二甲醚 为溶剂， 反应 47.0h， 生成 1-[4-(2,3-dihydro-1H-inden-1-yl)butyl]-3,3-dimethylpiperidine
  参考文献：
  名称：

  A multireceptorial binding reinvestigation on an extended class of σ ligands: N-[ω-(indan-1-yl and tetralin-1-yl)alkyl] derivatives of 3,3-dimethylpiperidine reveal high affinities towards σ1 and EBP sites

  摘要：

  New 1-[omega-(2,3-dihydro-1H-inden-1-yl)- and (2,3-dihydro-5-methoxy-1H-inden-1-yl)alkyl and 1-[omega-(1,2,3,4-tetrahydronaphthalen-1-yl)- and (6-methoxy- or 6-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)aIkyl] derivatives of 3,3-dimethylpiperidine were synthesized, as homologous compounds of an existing series of sigma ligands, in order to carry out sigma receptor subtypes structure-affinity relationships. The new compounds and some of their related analogues, already reported, were tested in new multi-receptorial radioligand binding assays. As reference compounds, the known sigma (1) ligands SA 4503, ED 1008 and NE 100 were also prepared and tested. All reported compounds showed high sigma (1) affinity assayed by (+)-[H-3]-pentazocine on guinea-pig brain (apparent K-i = 1.75-72.2 nM) and moderate or low sigma (2) affinity by [H-3]-DTG on rat liver, in contrast with previous results. One tertiary amine function spaced by a five-membered chain from a phenyl group is the structural feature shared by the most active compounds 26 and 43 and some reference al ligands. The reported ol ligands, including reference compounds, also demonstrated a high affinity towards EBP (Delta (8)-Delta (7) sterol isomerase) site (apparent K-i = 0.48-14.8 nM) and some of them (37 and 44) were good ligands at L-type Ca++ channel. 1-14-(2,3-Dihydro- 1H-inden-1-yl)butyl]-3,3-dimethylpiperidine (26) was the best mixed sigma (1) and EBP ligand (apparent K-i = 1.75 and 1.54 nM, respectively) with a good selectivity versus sigma (2) receptor (138- and 157-fold, respectively). (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(01)00011-6
• 作为产物：
  描述：

  2,2-二甲基戊二酸 在 氯化亚砜 作用下， 反应 5.0h， 生成 2,2-dimethylpentanedioyl dichloride
  参考文献：
  名称：

  N,N'-Di(8-quinolyl)glutaramide 通过液膜表现出高选择性和高效的 Cu(II) 上坡传输

  摘要：

  N,N'-Di(8-quinolyl)glutaramide 被发现是一种极好的 Cu(II) 载体，用于通过氯仿液膜的传输。它可以选择性、高效地从含有 Cu(II)、Zn(II)、Ni(II) 和 Co(II) 的弱酸性水溶液中传输 Cu(II)。已经制备了几种 N,N'-二（8-喹啉基）戊二酰胺衍生物及其类似物来比较这种运输能力，这在很大程度上不仅取决于载体的结构，还取决于运输条件。

  DOI：

  10.1246/bcsj.65.2381

文献信息

• [EN] DIMERIC IAP INHIBITORS<br/>[FR] INHIBITEURS IAP DIMÉRIQUES
  申请人：NOVARTIS AG

  公开号：WO2012080260A1

  公开（公告）日：2012-06-21

  The present invention provides compounds of formula M-L-M' (where M and M' are each independently a monomeric moiety of Formula (I), (II), (III) or (IV) and L is a linker). The dimeric compounds have been found to be effective in promoting apoptosis in rapidly dividing cells.

  本发明提供了公式M-L-M'的化合物（其中M和M'分别独立地是公式（I）、（II）、（III）或（IV）的单体基团，L是连接基团）。已发现二聚化合物在促进快速分裂细胞凋亡方面具有有效性。
• The Preparation of<i>N</i>-Acylpyrazoles and Their Behavior Toward Alcohols
  作者：Choji Kashima、Hajime Harada、Isanobu Kita、Iwao Fukuchi、Akira Hosomi

  DOI：10.1055/s-1994-25406

  日期：——

  According to four different methods, various types of N-acylpyrazoles were prepared from the corresponding pyrazoles and carboxylic acids or their acid chlorides. Although N-acylpyrazoles were inert to alcohols under neutral or weakly basic conditions, the alcoholysis was dramatically accelerated by the action of strong acid or base. On the basis of these chemical properties, the regioselective synthesis of methyl benzyl 2,2-dimethylglutarate was achieved by selective protection and functionalization of a carboxylic acid derivative using N-acylpyrazoles.

  根据四种不同的方法，从相应的吡唑和羧酸或其酰氯制备了多种类型的N-酰基吡唑。尽管在中性或弱碱性条件下，N-酰基吡唑对醇呈惰性，但强酸或碱的作用下，醇解反应显著加速。基于这些化学性质，通过选择性保护和功能化羧酸衍生物，成功实现了甲基苄基2,2-二甲基戊二酸酯的区域选择性合成。
• 7-azaindol-3-ylacrylamides active as kinase inhibitors
  申请人：NERVIANO MEDICAL SCIENCES S.r.l.

  公开号：EP2070928A1

  公开（公告）日：2009-06-17

  Compounds represented by Formula (I) wherein R1 and R2 are as defined in the specification, compositions thereof, and methods of use thereof.

  由式(I)表示的化合物，其中R1和R2如规范中定义，以及它们的组合物和使用方法。
• [EN] PHOSPHINYL AMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS<br/>[FR] COMPOSÉS DE PHOSPHINYLAMIDINE, COMPLEXES DE MÉTAL, SYSTÈMES DE CATALYSEUR, ET LEUR UTILISATION POUR OLIGOMÉRISER OU POLYMÉRISER DES OLÉFINES
  申请人：CHEVRON PHILLIPS CHEMICAL CO

  公开号：WO2011082192A1

  公开（公告）日：2011-07-07

  N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, N2-phosphinyl amidinate metal salt complexes are described. Methods for making N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes are also disclosed. Catalyst systems utilizing the N2-phosphinyl amidine metal salt complexes and N2-phosphinyl amidinate metal salt complexes are also disclosed along with the use of the N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes for the oligomerization and/or polymerization of olefins.

  描述了N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺金属盐络合物、N2-膦胺酸盐金属盐络合物。还公开了制备N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺金属盐络合物和N2-膦胺酸盐金属盐络合物的方法。还公开了利用N2-膦胺金属盐络合物和N2-膦胺酸盐金属盐络合物的催化剂系统，以及利用N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺金属盐络合物和N2-膦胺酸盐金属盐络合物进行烯烃的寡聚和/或聚合的用途。
• DIMERIC IAP INHIBITORS
  申请人：STRAUB Christopher Sean

  公开号：US20110206690A1

  公开（公告）日：2011-08-25

  The present invention provides compounds of formula M-L-M′ (where M and M′ are each independently a monomeric moiety of Formula (I) and L is a linker). The dimeric compounds have been found to be effective in promoting apoptosis in rapidly dividing cells.

  本发明提供了公式M-L-M′的化合物（其中M和M′分别是公式（I）中的单体基团，L是连接物）。已发现二聚化合物在促进快速分裂细胞凋亡方面具有有效性。