2-(4-(3-bromopropoxy)phenyl)benzo[d]oxazole | 1334551-92-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-(4-(3-bromopropoxy)phenyl)benzo[d]oxazole
• CAS: 1334551-92-6
• 化学式: C₁₆H₁₄BrNO₂
• 分子量: 332.197
• InChiKey: FSAATKLIZYSCHS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.66
• 重原子数：
  20.0
• 可旋转键数：
  5.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  35.26
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  2-(4-(3-bromopropoxy)phenyl)benzo[d]oxazole 在 tin(II) chloride dihdyrate 、 potassium carbonate 作用下， 以 甲醇 、 丙酮 为溶剂， 反应 53.0h， 生成
  参考文献：
  名称：

  PYRROLO[2,L-C][L,4]BENZODIAZEPINE-BENZOTHIAZOLE OR BENZOXAZOLE CONJUGATES LINKED THROUGH PIPERAZINE MOIETY AND PROCESS FOR THE PREPARATION THEREOF

  摘要：

  一种具有通式9的化合物，可作为潜在的抗人类癌细胞药剂，以及一种制备Pyrrolo[2,1-c][1,4]苯二氮杂环-苯并噻唑或苯并噁唑共轭物的方法，通过通式9中的哌嗪连接，其中：R，R1=H，F，OCF3，Cl，OMe；R2=OCH3或H；n1n2=3，4；x=S或O。

  公开号：

  US20120316335A1
• 作为产物：
  描述：

  对羟基苯甲酸 在 potassium carbonate 、 对甲苯磺酸 作用下， 以 5,5-dimethyl-1,3-cyclohexadiene 、 丙酮 为溶剂， 反应 12.0h， 生成 2-(4-(3-bromopropoxy)phenyl)benzo[d]oxazole
  参考文献：
  名称：

  Inhibition of cholinesterase activity and amyloid aggregation by berberine-phenyl-benzoheterocyclic and tacrine-phenyl-benzoheterocyclic hybrids

  摘要：

  A series of berberine-phenyl-benzoheterocyclic (26-29) and tacrine-phenyl-benzoheterocyclic hybrids (44-46) were synthesised and evaluated as multifunctional anti-Alzheimer's disease agents. Compound 44b, tacrine linked with phenyl-benzothiazole by 3-carbon spacers, was the most potent AChE inhibitor with an IC50 value of 0.017 mu M. This compound demonstrated similar A beta aggregation inhibitory activity with cucurmin (51.8% vs 52.1% at 20 mu M, respectively), indicating that this hybrid is an excellent multifunctional drug candidate for AD. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.02.059

文献信息

• [EN] PYRROLO[2,L-C][L,4]BENZODIAZEPINE-BENZOTHIAZOLE OR BENZOXAZOLE CONJUGATES LINKED THROUGH PIPERAZINE MOIETY AND PROCESS FOR THE PREPARATION THEREOF<br/>[FR] CONJUGUÉS DE PYRROLO[2,L-C][L,4]BENZODIAZÉPINE-BENZOTHIAZOLE OU DE BENZOXAZOLE LIÉS PAR UNE FRACTION PIPÉRAZINE ET LEUR PROCÉDÉ DE PRÉPARATION
  申请人：COUNCIL SCIENT IND RES

  公开号：WO2011117882A1

  公开（公告）日：2011-09-29

  The present invention provides a compound of general formula 9, useful as potential antitumour agents against human cancer cell lines. The present invention further provides a process for the preparation of Pyrrolo[2,l-c][l,4]benzodiazepine - benzothiazole or benzoxazole conjugates linked through piperazine of general formula (9) wherein: R, R1 = H, F, OCF3, CI, OMe; R2 = OCH3 or H; n1 n2= 3, 4; x = S or O

  本发明提供了一种通用式9的化合物，可作为潜在的抗人类癌细胞系的抗肿瘤剂。本发明还提供了一种制备Pyrrolo[2,1-c][1,4]苯并二氮杂环-苯并噻唑或苯并噁唑的共轭物的方法，通过通用式(9)中的哌嗪连接，其中：R，R1 = H，F，OCF3，Cl，OMe；R2 = OCH3或H；n1，n2 = 3，4；x = S或O。
• Synthesis and pharmacological evaluation of piperidine (piperazine)-substituted benzoxazole derivatives as multi-target antipsychotics
  作者：Ling Huang、Wenjun Zhang、Xiaohua Zhang、Lei Yin、Bangyin Chen、Jinchun Song

  DOI：10.1016/j.bmcl.2015.09.045

  日期：2015.11

  The present study describes the optimization of a series of novel benzoxazole-piperidine (piperazine) derivatives combining high dopamine D-2 and serotonin 5-HT1A, 5-HT2A receptor affinities. Of these derivatives, the pharmacological features of compound 29 exhibited high affinities for the DA D-2, 5-HT1A and 5-HT2A receptors, but low affinities for the 5-HT2C and histamine H-1 receptors and human ether-a-go-go-related gene (hERG) channels. Furthermore, compound 29 reduced apomorphine-induced climbing and 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI)-induced head twitching without observable catalepsy, even at the highest dose tested. Thus, compound 29 is a promising candidate as a multi-target antipsychotic treatment. (C) 2015 Elsevier Ltd. All rights reserved.