4-(Phenylcarbonylaminocarbonyl)amino-1-benzyl-piperidine | 76713-26-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 4-(Phenylcarbonylaminocarbonyl)amino-1-benzyl-piperidine
• 英文别名: N-[(1-benzylpiperidin-4-yl)carbamoyl]benzamide
• CAS: 76713-26-3
• 化学式: C₂₀H₂₃N₃O₂
• 分子量: 337.422
• InChiKey: VVQSDIAXLRLSBM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  61.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(Phenylcarbonylaminocarbonyl)amino-1-benzyl-piperidine 在 sodium hydroxide 、 1-氯乙基氯甲酸酯 、 三氟乙酸 作用下， 以 甲苯 为溶剂， 反应 67.0h， 生成 1,3-二氢-5-甲基-4-苯基-1-(4-哌啶基)-2H-咪唑-2-酮
  参考文献：
  名称：

  1-(3-Cyanobenzylpiperidin-4-yl)-5-methyl-4-phenyl-1,3-dihydroimidazol-2-one:  A Selective High-Affinity Antagonist for the Human Dopamine D₄ Receptor with Excellent Selectivity over Ion Channels

  摘要：

  After the requirement of pseudocycle formation in the ureas 3 and 7 for hD(4) binding and selectivity was confirmed, structural hybridization with the known hD(4) ligand 2 led to the design and identification of the lead 4-(2-oxo-1,3-dihydroimidazol-2-yl)piperidine . Optimization studies were carried out on 8 with the aim of achieving 1000-fold selectivity for hD(4) over all other receptors while retaining the good pharmacokinetic properties of the lead. After initial preparation of 8 as a minor component in a low-yielding reaction, a novel and regioselective "four-step/one-pot'' procedure was developed which proved to be applicable to rapid investigation of the SAR of the 1,3-dihydroimidazol-2-one ring. Various changes to substituents attached to the 3-, 4-, or B-position of the 1,3-dihydroimidazol-2-one core of 8 did not significantly improve selectivity for hD(4) over hD(2) and hD(3). Greater Selectivity( > 1000-foId) was ultimately achieved by meta substitution of the benzyl group of 8 with various substituents. Compounds 28, 31, and 32 all possess the required selectivity for hD(4) over the other dopamine subtypes, but only 32 has > 1000-fold selectivity over-all the key counterscreens we tested against. Compound 32 is an antagonist at hD(4) and has a good pharmacokinetic profile in the rat, with excellent estimated in vivo receptor occupancy, thus making it a potentially useful pharmacological tool to investigate the role of the D-4 receptor.

  DOI：

  10.1021/jm991029k
• 作为产物：
  描述：

  4-氨基-1-苄基哌啶 、 苯甲酰异氰酸脂 在 ice 、 乙醚 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以to give the required product as a white solid 15.4 g (87%)的产率得到4-(Phenylcarbonylaminocarbonyl)amino-1-benzyl-piperidine
  参考文献：
  名称：

  Imidazolone and oxazolone derivatives as dopamine antagonists

  摘要：

  一类结构为I的咪唑酮和噁唑酮衍生物，其中X代表氧或N-R.sup.1; Q代表一种取代的五元、六元或七元单环杂脂环，其中含有一个氮原子作为唯一的杂原子，并通过碳原子与咪唑酮或噁唑酮环相连；R.sup.1代表氢或C.sub.1-6烷基；R.sup.2和R.sup.3中的一个代表氢或C.sub.1-6烷基，另一个代表环烷基或公式(i)、(ii)或(iii)的基团：##STR2## 其中Z代表氧、硫或NH；R.sup.4、R.sup.5和R.sup.6独立地代表氢、烃基或杂环基，其中所述的烃基和杂环基在说明书中有定义；或其药学上可接受的盐或前药，它们是大脑内多巴胺受体亚型的配体，因此可用于治疗和/或预防多巴胺系统的疾病，如精神分裂症。

  公开号：

  US05698573A1

文献信息

• Imidazolone and oxazolone derivatives as dopamine antagonists
  申请人：Merck, Sharp & Dohme, Ltd.

  公开号：US05698573A1

  公开（公告）日：1997-12-16

  A class of imidazolone and oxazolone derivatives of Structure I, ##STR1## wherein X represents oxygen or N--R.sup.1 ; Q represents a substituted five-, six- or seven-membered monocyclic heteroaliphatic ring which contains one nitrogen atom as the sole heteroatom and is linked to the imidazolone or oxazolone ring via a carbon atom; R.sup.1 represents hydrogen or C.sub.1-6 alkyl; and one of R.sup.2 and R.sup.3 represents hydrogen or C.sub.1-6 alkyl and the other of R.sup.2 and R.sup.3 represents cycloalkyl or a group of formula (i), (ii) or (iii): ##STR2## in which Z represents oxygen, sulphur or NH; R.sup.4, R.sup.5 and R.sup.6 independently represent hydrogen, a hydrocarbon group or a heterocyclic group wherein the hydrocarbon group and heterocyclic group are as defined in the specification; or a pharmaceutically acceptable salt or prodrug thereof, which are ligands for dopamine receptor subtypes within the brain and are therefore of use in the treatment and/or prevention of disorders of the dopamine system, such as schizophrenia.

  I. 结构的咪唑酮和噁唑酮衍生物类，其中X代表氧或N--R.sup.1；Q代表一种取代的五、六或七元杂环脂肪环，其中含有一个氮原子作为唯一杂原子，并通过一个碳原子连接到咪唑酮或噁唑酮环上；R.sup.1代表氢或C.sub.1-6烷基；R.sup.2和R.sup.3中的一个代表氢或C.sub.1-6烷基，另一个代表环烷基或式(i)、(ii)或(iii)的基团：##STR2## 其中Z代表氧、硫或NH；R.sup.4、R.sup.5和R.sup.6独立地代表氢、烃基或杂环基，其中烃基和杂环基如规范中定义；或其药学上可接受的盐或前药，它们是大脑内多巴胺受体亚型的配体，因此可用于治疗和/或预防多巴胺系统紊乱，如精神分裂症。
• IMIDAZOLONE AND OXAZOLONE DERIVATIVES AS DOPAMINE ANTAGONISTS
  申请人：MERCK SHARP & DOHME LTD.

  公开号：EP0719264B1

  公开（公告）日：1997-12-29
• US5698573A
  申请人：——

  公开号：US5698573A

  公开（公告）日：1997-12-16
• 1-(3-Cyanobenzylpiperidin-4-yl)-5-methyl-4-phenyl-1,3-dihydroimidazol-2-one:  A Selective High-Affinity Antagonist for the Human Dopamine D₄ Receptor with Excellent Selectivity over Ion Channels
  作者：Robert W. Carling、Kevin W. Moore、Christopher R. Moyes、Elizabeth A. Jones、Katrine Bonner、Frances Emms、Rosemary Marwood、Shil Patel、Smita Patel、Alan E. Fletcher、Margaret Beer、Bindi Sohal、Andrew Pike、Paul D. Leeson

  DOI：10.1021/jm991029k

  日期：1999.7.1

  After the requirement of pseudocycle formation in the ureas 3 and 7 for hD(4) binding and selectivity was confirmed, structural hybridization with the known hD(4) ligand 2 led to the design and identification of the lead 4-(2-oxo-1,3-dihydroimidazol-2-yl)piperidine . Optimization studies were carried out on 8 with the aim of achieving 1000-fold selectivity for hD(4) over all other receptors while retaining the good pharmacokinetic properties of the lead. After initial preparation of 8 as a minor component in a low-yielding reaction, a novel and regioselective "four-step/one-pot'' procedure was developed which proved to be applicable to rapid investigation of the SAR of the 1,3-dihydroimidazol-2-one ring. Various changes to substituents attached to the 3-, 4-, or B-position of the 1,3-dihydroimidazol-2-one core of 8 did not significantly improve selectivity for hD(4) over hD(2) and hD(3). Greater Selectivity( > 1000-foId) was ultimately achieved by meta substitution of the benzyl group of 8 with various substituents. Compounds 28, 31, and 32 all possess the required selectivity for hD(4) over the other dopamine subtypes, but only 32 has > 1000-fold selectivity over-all the key counterscreens we tested against. Compound 32 is an antagonist at hD(4) and has a good pharmacokinetic profile in the rat, with excellent estimated in vivo receptor occupancy, thus making it a potentially useful pharmacological tool to investigate the role of the D-4 receptor.