2-Methoxy-5,6,7,8-tetrahydro-naphthalene-1-carbonyl chloride | 274929-65-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-Methoxy-5,6,7,8-tetrahydro-naphthalene-1-carbonyl chloride
• 英文别名: 2-Methoxy-5,6,7,8-tetrahydro-1-naphthalenecarbonyl chloride；2-methoxy-5,6,7,8-tetrahydronaphthalene-1-carbonyl chloride
• CAS: 274929-65-6
• 化学式: C₁₂H₁₃ClO₂
• 分子量: 224.687
• InChiKey: RKBFNBCMAGYJLJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-Methoxy-5,6,7,8-tetrahydro-naphthalene-1-carbonyl chloride 在 盐酸 、 正丁基锂 作用下， 以 四氢呋喃 、 正己烷 、 乙酸乙酯 、 甲苯 为溶剂， 反应 19.0h， 生成 (S)-2-(1-azabicyclo[2.2.2]oct-3-yl)-2,4,5,6-tetrahydro-9-methoxy-1H-benz[de]isoquinolin-1-one
  参考文献：
  名称：

  2-(Quinuclidin-3-yl)pyrido[4,3-b]indol-1-ones and isoquinolin-1-ones. Potent conformationally restricted 5-HT3 receptor antagonists

  摘要：

  Several series of N-(quinuclidin-3-yl)aryl and heteroaryl-fused pyridones were synthesized and evaluated for 5-HT3 receptor affinity. In the heteroaryl series, 2-(quinuclidin-3-yl)tetrahydropyrido-[4,3-b]indol-1-one (8a) and the 4,5-alkano-bridged analogues (14 and 15) displayed high 5-HT3 receptor affinity with pK(i) values > 9. The (3S)-quinuclidinyl isomers had > 10 fold higher affinity than the (3R)-isomers. In a series of 2-quinuclidin-3-yl)isoquinolin-1-ones, derivatives substituted with small lipophilic groups (25b-e) and with 4,5-alkano-bridges (34-36) also displayed high affinity. In particular, the hexahydro-1H-benz[de]isoquinolinone (S,S)-37 was the highest affinity 5-HT3 receptor ligand prepared (pK(i) 10.4). A number of the high affinity ligands were shown to be potent 5-HT3 receptor antagonists in vivo as determined by inhibition of the B-J reflex in the anesthetized rat. Again, (S,S)-37 was the most active agent tested (ID50 0.02 mug/kg iv), and this compound was also potent in blocking cisplatin-induced emesis in both the ferret and the dog. Computer modeling studies were performed, and previously reported 5-HT3 receptor antagonist pharmacophore models were refined to include a key lipophilic binding domain.

  DOI：

  10.1021/jm00070a008
• 作为产物：
  描述：

  2-methoxy-5,6,7,8-tetrahydronaphthoic acid 在 氯化亚砜 、 N,N-二甲基甲酰胺 作用下， 以 甲苯 为溶剂， 反应 2.0h， 生成 2-Methoxy-5,6,7,8-tetrahydro-naphthalene-1-carbonyl chloride
  参考文献：
  名称：

  2-(Quinuclidin-3-yl)pyrido[4,3-b]indol-1-ones and isoquinolin-1-ones. Potent conformationally restricted 5-HT3 receptor antagonists

  摘要：

  Several series of N-(quinuclidin-3-yl)aryl and heteroaryl-fused pyridones were synthesized and evaluated for 5-HT3 receptor affinity. In the heteroaryl series, 2-(quinuclidin-3-yl)tetrahydropyrido-[4,3-b]indol-1-one (8a) and the 4,5-alkano-bridged analogues (14 and 15) displayed high 5-HT3 receptor affinity with pK(i) values > 9. The (3S)-quinuclidinyl isomers had > 10 fold higher affinity than the (3R)-isomers. In a series of 2-quinuclidin-3-yl)isoquinolin-1-ones, derivatives substituted with small lipophilic groups (25b-e) and with 4,5-alkano-bridges (34-36) also displayed high affinity. In particular, the hexahydro-1H-benz[de]isoquinolinone (S,S)-37 was the highest affinity 5-HT3 receptor ligand prepared (pK(i) 10.4). A number of the high affinity ligands were shown to be potent 5-HT3 receptor antagonists in vivo as determined by inhibition of the B-J reflex in the anesthetized rat. Again, (S,S)-37 was the most active agent tested (ID50 0.02 mug/kg iv), and this compound was also potent in blocking cisplatin-induced emesis in both the ferret and the dog. Computer modeling studies were performed, and previously reported 5-HT3 receptor antagonist pharmacophore models were refined to include a key lipophilic binding domain.

  DOI：

  10.1021/jm00070a008
• 作为试剂：
  描述：

  2-methoxy-5,6,7,8-tetrahydronaphthoic acid 、 草酰氯 在 N,N-二甲基甲酰胺 2-Methoxy-5,6,7,8-tetrahydro-naphthalene-1-carbonyl chloride 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 生成 2-Methoxy-5,6,7,8-tetrahydro-naphthalene-1-carbonyl chloride
  参考文献：
  名称：

  N-(2-phenyl-4-piperidinybutyl)-5,6,7,8-tetrahydro-1-naphthalenecarboxamides and their use as neurokinin 1 (NK1) and/or neurokinin 2 (NK2) receptor antagonists

  摘要：

  式(I)的化合物，其中R2是5,6,7,8-四氢萘-1-基基团，该基团可以被取代（其余在此定义的基团），以及含有该化合物的制药组合物和使用该化合物治疗拮抗NK1和/或NK2受体有益的疾病的方法。

  公开号：

  US06403601B1

文献信息

• [EN] AMINE OR (THIO)AMIDE CONTAINING LXR MODULATORS<br/>[FR] MODULATEURS DE LXR À BASE D'AMINE OU DE (THIO) AMIDE
  申请人：PHENEX FXR GMBH

  公开号：WO2019016269A1

  公开（公告）日：2019-01-24

  The present invention relates to derivatives of formula (I) which bind to the liver X receptor (LXRα and/or LXRβ) and act preferably as inverse agonists of LXR.

  本发明涉及公式（I）的衍生物，其结合到肝X受体（LXRα和/或LXRβ），并且作为LXR的拮抗剂。
• N-(2-PHENYL-4-PIPERIDINYLBUTYL)-5,6,7,8-TETRAHYDRO-1-NAPHTHALENECARBOXAMIDES AND THEIR USE AS NEUROKININ 1 (NK1) AND/OR NEUROKININ 2 (NK2) RECEPTOR ANTAGONISTS
  申请人：AstraZeneca AB

  公开号：EP1137637A1

  公开（公告）日：2001-10-04
• AMINE OR (THIO)AMIDE CONTAINING LXR MODULATORS
  申请人：Phenex-FXR GmbH

  公开号：US20200131144A1

  公开（公告）日：2020-04-30

  The present invention relates to derivatives of formula (I) which bind to the liver X receptor (LXRα and/or LXRβ) and act preferably as inverse agonists of LXR.
• US6403601B1
  申请人：——

  公开号：US6403601B1

  公开（公告）日：2002-06-11
• [EN] N-(2-PHENYL-4-PIPERIDINYBUTYL)-5,6,7,8-TETRAHYDRO-1-NAPHTHALENECARBOXAMIDES AND THEIR USE AS NEUROKININ 1 (NK1) AND/OR NEUROKININ 2 (NK2) RECEPTOR ANTAGONISTS<br/>[FR] N-(2-PHENYLE-4-PIPERIDINYBUTYLE)-5,6,7,8-TETRAHYDRO-1-NAPTHALENE CARBOXAMIDES ET LEUR UTILISATION COMME ANTAGONISTES DES RECEPTEURS DE LA NEUROKININE 1 (NK1) ET/OU DE LA NEUROKININE 2 (NK2)
  申请人：ASTRAZENECA UK LTD

  公开号：WO2000034243A1

  公开（公告）日：2000-06-15

  Compounds of formula (I), wherein R2 is a 5,6,7,8-tetrahydronaphth-1-yl group which may be substituted (the remaining groups defined herein), and pharmaceutical compositions containing the compounds and methods of using the compounds in the treatment of a condition where antagonism of the NK1 and/or NK2 receptors is beneficial.