tert-Butyl cis-4-(2-oxoethyl)cyclohexylcarbamate | 847417-37-2

• 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: tert-Butyl cis-4-(2-oxoethyl)cyclohexylcarbamate
• 英文别名: tert-butyl ((1s,4s)-4-(2-oxoethyl)cyclohexyl)carbamate；tert-butyl (cis-4-(2-oxoethyl)cyclohexyl)carbamate；tert-butyl 4-(2-oxoethyl)cyclohexylcarbamate；cis-Boc-2-(4-aminocyclohexyl)acetaldehyde
• CAS: 847417-37-2
• 化学式: C₁₃H₂₃NO₃
• 分子量: 241.331
• InChiKey: OPGBSEXLSWYFOR-PHIMTYICSA-N

物化性质

• 沸点：
  360.6±11.0 °C(Predicted)
• 密度：
  1.02±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.66
• 重原子数：
  17.0
• 可旋转键数：
  3.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.85
• 拓扑面积：
  55.4
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  tert-Butyl cis-4-(2-oxoethyl)cyclohexylcarbamate 在 三乙酰氧基硼氢化钠 、 三氟乙酸 作用下， 以 二氯甲烷 、 1,2-二氯乙烷 为溶剂， 生成 cis-4-(2-(3,4-dihydroisoquinolin-2(1H)-yl)ethyl)cyclohexanamine
  参考文献：
  名称：

  A Structure–Activity Analysis of Biased Agonism at the Dopamine D2 Receptor

  摘要：

  Biased agonism offers an opportunity for the medicinal chemist to discover pathway-selective ligands for GPCRs. A number of studies have suggested that biased agonism at the dopamine D2 receptor (D2R) may be advantageous for the treatment of neuropsychiatric disorders, including schizophrenia. As such, it is of great importance to gain insight into the SAR of biased agonism at this receptor. We have generated SAR based on a novel D2R partial agonist, tert-butyl (trans-4-(2-(3,4dihydroisoquinolin-2(1H)-yOethyl)cyclohexyl)carbamate (4). This ligand shares structural similarity to cariprazine (2), a drug awaiting FDA approval for the treatment of schizophrenia, yet displays a distinct bias toward two different signaling end points. We synthesized a number of derivatives of 4 with subtle structural modifications, including incorporation of cariprazine fragments. By combining pharmacological profiling with analytical methodology to identify and to quantify bias, we have demonstrated that efficacy and biased agonism can be finely tuned by minor structural modifications to the head group containing the tertiary amine, a tail group that extends away from this moiety, and the orientation and length of a spacer region between these two moieties.

  DOI：

  10.1021/jm401318w
• 作为产物：
  描述：

  ethyl 2-(cis-4-((tert-butoxycarbonyl)amino)cyclohexyl)acetate 在 二异丁基氢化铝 作用下， 以 甲苯 为溶剂， 以96%的产率得到tert-Butyl cis-4-(2-oxoethyl)cyclohexylcarbamate
  参考文献：
  名称：

  A Structure–Activity Analysis of Biased Agonism at the Dopamine D2 Receptor

  摘要：

  Biased agonism offers an opportunity for the medicinal chemist to discover pathway-selective ligands for GPCRs. A number of studies have suggested that biased agonism at the dopamine D2 receptor (D2R) may be advantageous for the treatment of neuropsychiatric disorders, including schizophrenia. As such, it is of great importance to gain insight into the SAR of biased agonism at this receptor. We have generated SAR based on a novel D2R partial agonist, tert-butyl (trans-4-(2-(3,4dihydroisoquinolin-2(1H)-yOethyl)cyclohexyl)carbamate (4). This ligand shares structural similarity to cariprazine (2), a drug awaiting FDA approval for the treatment of schizophrenia, yet displays a distinct bias toward two different signaling end points. We synthesized a number of derivatives of 4 with subtle structural modifications, including incorporation of cariprazine fragments. By combining pharmacological profiling with analytical methodology to identify and to quantify bias, we have demonstrated that efficacy and biased agonism can be finely tuned by minor structural modifications to the head group containing the tertiary amine, a tail group that extends away from this moiety, and the orientation and length of a spacer region between these two moieties.

  DOI：

  10.1021/jm401318w

文献信息

• [EN] ACYLAMINOCYCLOALKYL COMPOUNDS SUITABLE FOR TREATING DISORDERS THAT RESPOND TO MODULATION OF DOPAMINE D3 RECEPTOR<br/>[FR] COMPOSÉS D'ACYLAMINOCYCLOALKYLE APPROPRIÉS POUR LE TRAITEMENT DE TROUBLES RÉPONDANT À LA MODULATION DU RÉCEPTEUR D3 DE LA DOPAMINE
  申请人：ABBVIE DEUTSCHLAND

  公开号：WO2014064038A1

  公开（公告）日：2014-05-01

  The present invention relates to novel acylaminocycloalkyl compounds, in particular to the compounds of the formula (I) as described herein and to their salts and N-oxides. The compounds possess valuable therapeutic properties and are suitable, in particular, for treating diseases that respond to modulation of the dopamine D3 receptor. In formula (I), the variables have the following meanings: m is 1 or 2, n is 1 or 2, A is selected from the group consisting of CH2, CH2CH2, CHFCH2 and CF2CH2, R1 is hydrogen or C1-C3-alkyl, R2 is selected from the group consisting of hydrogen, and fluorine, R3a is selected from the group consisting of hydrogen and methyl, R3b is selected from the group consisting of hydrogen and methyl, R4 is branched C4-C6 alkyl or branched fluorinated C4-C6 alkyl, and R5 is an oxygen containing radical such as C1-C2-alkoxy-C1-C4-alkyl, fluorinated C1-C2-alkoxy-C1-C4-alkyl, hydroxy-C1-C4-alkyl, fluorinated hydroxy-C1-C4-alkyl, oxetanyl, fluorinated oxetanyl, oxolanyl, fluorinated oxolanyl, C3-C5 cycloalkyl, fluorinated C3-C5 cycloalkyl, C3-C5 cycloalkoxy-C1-C4-alkyl and fluorinated C3-C5 cycloalkoxy-C1-C4-alkyl.

  本发明涉及新型酰胺环烷基化合物，特别是本文所述的具有以下式（I）的化合物及其盐和N-氧化物。这些化合物具有有价值的治疗性能，并且特别适用于治疗对多巴胺D3受体调节产生反应的疾病。在式（I）中，变量具有以下含义：m为1或2，n为1或2，A从CH2、 、CHF 和CF2 组成的群体中选择，R1为氢或C1-C3-烷基，R2从氢和氟中选择，R3a从氢和甲基中选择，R3b从氢和甲基中选择，R4为支链C4-C6烷基或支链氟化C4-C6烷基，R5为含氧基团，例如C1-C2-烷氧基-C1-C4-烷基，氟化C1-C2-烷氧基-C1-C4-烷基，羟基-C1-C4-烷基，氟化羟基-C1-C4-烷基，氧杂环丙基，氟化氧杂环丙基，氧杂环戊基，氟化氧杂环戊基，C3-C5环烷基，氟化C3-C5环烷基，C3-C5环烷氧基-C1-C4-烷基和氟化C3-C5环烷氧基-C1-C4-烷基。
• Antitumor Compounds Based on a Natural Product Consensus Pharmacophore
  作者：Chandraiah Lagisetti、Alan Pourpak、Qin Jiang、Xiaoli Cui、Tinopiwa Goronga、Stephan W. Morris、Thomas R. Webb

  DOI：10.1021/jm8006195

  日期：2008.10.9

  We report the design and highly enantioselective synthesis of a potent analogue of the spliceosome inhibitor FR901464, based on a non-natural product scaffold. The design of this compound was facilitated by a pharmacophore hypothesis that assumed key interaction types that are common to FR901464 and an otherwise unrelated natural product (pladienolide). The synthesis allows for the preparation of numerous

  我们报告了基于非天然产物支架的剪接体抑制剂 FR901464 的有效类似物的设计和高度对映选择性合成。药效团假设促进了该化合物的设计，该假设假设了 FR901464 和其他不相关的天然产物（pladienolide）共有的关键相互作用类型。该合成允许制备许多新型类似物。我们展示了该化合物对几种肿瘤细胞系的体外活性结果。
• ANTICANCER COMPOUNDS AND METHODS OF MAKING AND USING SAME
  申请人：Webb Thomas R.

  公开号：US20110178098A1

  公开（公告）日：2011-07-21

  In one aspect, the invention relates to compounds having anticancer activity; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating disorders associated with uncontrolled cellular proliferation using the compounds and compositions. This abstract is intended to be used as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  本发明涉及具有抗癌活性的化合物；制备这些化合物的合成方法；包含这些化合物的药物组合物；以及使用这些化合物和组合物治疗与细胞不受控制增殖相关的疾病的方法。本摘要旨在用作扫描工具，用于在特定领域进行搜索，并不意味着对本发明的限制。
• ACYLAMINOCYCLOALKYL COMPOUNDS SUITABLE FOR TREATING DISORDERS THAT RESPOND TO MODULATION OF DOPAMINE D3 RECEPTOR
  申请人：AbbVie Inc.

  公开号：US20140303176A1

  公开（公告）日：2014-10-09

  The present invention relates to novel acylaminocycloalkyl compounds, in particular to the compounds of the formula I as described herein and to their salts and N-oxides. The compounds possess valuable therapeutic properties and are suitable, in particular, for treating diseases that respond to modulation of the dopamine D3 receptor. In formula I, the variables have the following meanings: m is 1 or 2, n is 1 or 2, A is selected from the group consisting of CH 2 , CH 2 CH 2 , CHFCH 2 and CF 2 CH 2 , R 1 is an oxygen containing cyclic radical selected such as C 3 -C 6 cycloalkyl, which carries one or two oxygen containing radicals selected from the group consisting of OH, C 1 -C 2 -alkoxy, fluorinated C 1 -C 2 -alkoxy, and a carbonyl oxygen, R 2 is selected from the group consisting of hydrogen, OH and fluorine, R 3a is selected from the group consisting of hydrogen and methyl, R 3b is selected from the group consisting of hydrogen and methyl, R 4 is branched C 4 -C 6 alkyl or branched fluorinated C 4 -C 6 alkyl, and R 5 is inter alia C 1 -C 6 alkyl, fluorinated C 1 -C 3 alkyl, C 1 -C 2 -alkoxy-C 1 -C 4 -alkyl, fluorinated C 1 -C 2 -alkoxy-C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkyl, fluorinated hydroxy-C 1 -C 4 -alkyl, oxetanyl, fluorinated oxetanyl, oxolanyl, fluorinated oxolanyl, C 3 -C 5 cycloalkyl, fluorinated C 3 -C 5 cycloalkyl, etc.

  本发明涉及新颖的酰基氨基环烷化合物，特别是如下式I所述的化合物及其盐和N-氧化物。这些化合物具有有价值的治疗特性，特别适用于治疗对多巴胺D3受体调节有反应的疾病。在式I中，变量具有以下含义：m为1或2，n为1或2，A选自CH2、 、CHF 和CF2 组成的群，R1为含氧环基，选自C3-C6环烷基，其携带一个或两个选自OH、C1-C2-烷氧基、氟化C1-C2-烷氧基和一个羰基氧的含氧基团，R2选自氢、OH和氟，R3a选自氢和甲基，R3b选自氢和甲基，R4为支链C4-C6烷基或支链氟化C4-C6烷基，R5包括C1-C6烷基、氟化C1-C3烷基、C1-C2-烷氧基-C1-C4-烷基、氟化C1-C2-烷氧基-C1-C4-烷基、羟基-C1-C4-烷基、氟化羟基-C1-C4-烷基、氧杂环丙基、氟化氧杂环丙基、氧杂环戊基、氟化氧杂环戊基、C3-C5环烷基、氟化C3-C5环烷基等。
• 1,3-BENZODIOXOLE DERIVATIVE
  申请人：Daiichi Sankyo Company, Limited

  公开号：EP3121175A1

  公开（公告）日：2017-01-25

  The present invention provides a compound having a particular chemical structure or a pharmacologically acceptable salt thereof which has an excellent inhibitory effect on EZH1 and/or EZH2 activity. The present invention provides a compound having a 1,3-benzodioxole structure represented by the general formula (I) or a pharmacologically acceptable salt thereof, or a pharmaceutical composition comprising the compound (wherein R1, R2, R3, R4, R5, R6, and V in the formula (I) are each as defined in the present specification).

  本发明提供了一种具有特定化学结构的化合物或其药理学上可接受的盐，该化合物对 EZH1 和/或 EZH2 的活性具有极佳的抑制作用。本发明提供了一种具有通式（I）所代表的 1，3-苯并二恶茂结构的化合物或其药理学上可接受的盐，或包含该化合物的药物组合物（其中式（I）中的 R1、R2、R3、R4、R5、R6 和 V 均如本说明书中所定义）。