N-(4-oxotetralin-6-yl)benzamide | 163465-76-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: N-(4-oxotetralin-6-yl)benzamide
• 英文别名: N-(5,6,7,8-tetrahydro-8-oxonaphthalen-2-yl)benzamide；N-(8-oxo-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzamide；7-benzamido-α-tetralone；N-(8-oxo-6,7-dihydro-5H-naphthalen-2-yl)benzamide
• CAS: 163465-76-7
• 化学式: C₁₇H₁₅NO₂
• 分子量: 265.312
• InChiKey: CZSWDIGLLXPCSM-UHFFFAOYSA-N

物化性质

• 沸点：
  365.8±31.0 °C(Predicted)
• 密度：
  1.253±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  46.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-(4-oxotetralin-6-yl)benzamide 、 甲基三苯基溴化膦 在 potassium tert-butylate 作用下， 以 甲苯 为溶剂， 反应 4.0h， 以58%的产率得到N-(4-methylenetetralin-6-yl)benzamide
  参考文献：
  名称：

  [EN] SPIROCYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A
  [FR] DÉRIVÉS DE SPIROCYCLOPROPYLAMINE UTILES EN TANT QU'INHIBITEURS D'HISTONE DÉMÉTHYLASES KDM1A

  摘要：

  本发明涉及提供的螺环环丙胺化合物，具有强效的KDM1A（LSD1）抑制活性，其中X、R和R1如规范中所定义，包含这种化合物的药物组合物以及它们在治疗中的应用。

  公开号：

  WO2017109061A1
• 作为产物：
  描述：

  7-氨基-1-四氢萘酮 、 苯甲酰氯 在 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 5.0h， 以70.5%的产率得到N-(4-oxotetralin-6-yl)benzamide
  参考文献：
  名称：

  [EN] SPIROCYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A
  [FR] DÉRIVÉS DE SPIROCYCLOPROPYLAMINE UTILES EN TANT QU'INHIBITEURS D'HISTONE DÉMÉTHYLASES KDM1A

  摘要：

  本发明涉及提供的螺环环丙胺化合物，具有强效的KDM1A（LSD1）抑制活性，其中X、R和R1如规范中所定义，包含这种化合物的药物组合物以及它们在治疗中的应用。

  公开号：

  WO2017109061A1

文献信息

• Pyrazinyl-substituted naphthalene derivatives
  申请人：——

  公开号：US20010004669A1

  公开（公告）日：2001-06-21

  Compounds of the formula 1 where R 1 is of the formulae 2 R 2 is —R 4 , —O—R 4 , —O—S (O) 2 —R 4 , —NR 4 R 5 , R 4 —(CH 2 ) b —NH(C═X)—(CH 2 )—, R 4 —(CH 2 ) b —O(C═O)NH—(CH 2 ) c —(C═O)NH—, R 4 (C═O)NH—(C═O)NH—, —(CH 2 ) b —NH(C═X)—(CH 2 ) c —R 4 , R 4 —(CH 2 ) b —O(C═)—(CH 2 ) c —, —(CH 2 ) b —O(C═O)—(CH 2 ) c —R 4 , —NH(C═X)NH—R 4 , R 4 —O(C═O)O—, —O(C═)NH—R 4 , R 4 —O(C═O)NH—, —(CH 2 ) b —(C═0)—(CH 2 ) c —R 4 , —NH—S(O) 2 —R 4 , —C(OH)R 4 R 5 , —CH(OH)—R 4 , —(C═O)—NR 4 R 5 , —CN, —NO 2 , substituted C 1 to C 6 alkyl, substituted or unsubstituted C 1 to C 6 alkenyl, or substituted or unsubstituted C 1 to C 6 alkynyl, said substituted moieties substituted with a moiety of the formulae —R 4 , —R 4 R 5 , —O—R 4 , or —S(O) d —R 4 . These compounds are useful psychotherapeutics and are potent serotonin (5-HT 1 ) agonists and antagonists and may be used in the treatment of depression, anxiety, eating disorders, obesity, drug abuse, cluster headache, migraine, pain and chronic paroxysmal hemicrania and headache associated with vascular disorders, and other disorders arising from deficient serotonergic neurotranmission. The compounds can also be used as centrally acting antihypertensives and vasodilators.

  公式1的化合物，其中R1是公式2，R2是—R4，—O—R4，—O—S(O)2—R4，—NR4R5，R4—(CH2)b—NH(C═X)—( )c—，R4—( )b—O(C═O)NH—( )c—(C═O)NH—，R4(C═O)NH—(C═O)NH—，—( )b—NH(C═X)—( )c—R4，R4—( )b—O(C═)—( )c—，—( )b—O(C═O)—( )c—R4，—NH(C═X)NH—R4，R4—O(C═O)O—，—O(C═)NH—R4，R4—O(C═O)NH—，—( )b—(C═O)—( )c—R4，—NH—S(O)2—R4，—C(OH)R4R5，—CH(OH)—R4，—(C═O)—NR4R5，—CN，—NO2，取代的C1至C6烷基，取代或未取代的C1至C6烯基，或取代或未取代的C1至C6炔基，所述取代基团被公式—R4，—R4R5，—O—R4或—S(O)d—R4的基团取代。这些化合物是有用的精神治疗剂，并且是强效的血清素（5-HT1）激动剂和拮抗剂，可用于治疗抑郁症、焦虑症、饮食失调、肥胖、药物滥用、丛集性头痛、偏头痛、疼痛和慢性阵发性偏头痛以及与血管疾病相关的头痛，以及其他由血清素神经传递不足引起的疾病。这些化合物还可用作中枢作用抗高血压药和血管扩张剂。
• Compositions containing sertraline and a 5-HT.sub.1D receptor agonist or
  申请人：Pfizer Inc.

  公开号：US05597826A1

  公开（公告）日：1997-01-28

  The present invention relates to novel compositions containing the serotonin selective re-uptake inhibitor (SSRI), preferably (1S-cis)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenam ine, and an agonist or antagonist of the serotonin 1 (5-HT.sub.1) receptor and to the use of such compositions for treating or preventing a condition selected from mood disorders, including depression, seasonal affective disorders and dysthmia, anxiety disorders including generalized anxiety disorder and panic disorder; agoraphobia, avoidant personality disorder; social phobia; obsessive compulsive disorder; post-traumatic stress disorder; memory disorders including dementia, amnestic disorders and age-associated memory impairment; disorders of eating behavior, including anorexia nervosa and bulimia nervosa; obesity; cluster headache; migraine; pain; Alzheimer's disease; chronic paroxysmal hemicrania; headache associated with vascular disorders; Parkinson's disease, including dementia in Parkinson's disease, neuroleptic-induced parkinsonism and tardive dyskinesias; endocrine disorders such as hyperprolactinaemia; vasospasm (particularly in the cerebral vasculature); hypertension; disorders in the gastrointestinal tract where changes in motility and secretion are involved; sexual dysfunction, including premature ejaculation; and chemical dependencies.

  本发明涉及包含选择性5-羟色胺再摄取抑制剂（SSRI），优选（1S-顺）-4-(3,4-二氯苯基)-1,2,3,4-四氢-N-甲基-1-萘胺，以及5-羟色胺1（5-HT1）受体的激动剂或拮抗剂的新组合物，以及使用这样的组合物治疗或预防情绪障碍，包括抑郁症、季节性情感障碍和情绪恶劣，焦虑障碍，包括广泛性焦虑障碍和恐慌障碍；恐旷症，回避性人格障碍；社交恐惧症；强迫症；创伤后应激障碍；记忆障碍，包括痴呆、遗忘障碍和与年龄相关的记忆减退；饮食行为障碍，包括厌食症和贪食症；肥胖；丛集性头痛；偏头痛；疼痛；阿尔茨海默病；慢性阵发性偏头痛；与血管疾病相关的头痛；帕金森病，包括帕金森病性痴呆、神经阻滞剂诱发的帕金森综合症和迟发性运动障碍；内分泌障碍，如高催乳素血症；血管痉挛（特别是在脑血管中）；高血压；涉及运动和分泌变化的胃肠道疾病；性功能障碍，包括早泄；以及化学依赖性。
• [EN] TETRAHYDRONAPHTHYL- PIPERAZINES AS 5-HT1B ANTAGONISTS, INVERSE AGONISTS AND PARTIAL AGONISTS<br/>[FR] TETRAHYDRONAPHTHYLPIPER- AZINES UTILISEES EN TANT QU'AGONISTES INVERSES, AGONISTES PARTIELS ET ANTAGONISTES DE 5-HT1B
  申请人：PFIZER PROD INC

  公开号：WO2005113527A1

  公开（公告）日：2005-12-01

  The present invention relates to novel tetrahydronaphthylpiperazines derivatives, that are compounds of the formula (I) wherein R1, R2 and R6 are as defined herein, X is CH2 or O, A is a group of the formula (G1, G2, G2a, G3, G4, G5 or G6) depicted below, and D is a group of the formula (D), wherein Y, W and Z are C or N and wherein R7 is as defined herein and their salts and compositions which include selective antagonists, inverse agonists and partial agonists of serotonin 1 (5-HT1) receptors. Compounds of the invention are useful in treating or preventing depression, anxiety, obsessive compulsive disorder (OCD) and other disorders for which a 5-HT1 agonist or antagonist is indicated.

  本发明涉及新型四氢萘哌嗪衍生物，即式(I)中R1、R2和R6如本文所定义，X为CH2或O，A为下图所示的式(G1、G2、G2a、G3、G4、G5或G6)的基团，D为式(D)的基团，其中Y、W和Z为C或N，R7如本文所定义，以及它们的盐和组合物，包括选择性5-羟色胺1(5-HT1)受体的拮抗剂、逆向激动剂和部分激动剂。本发明的化合物在治疗或预防抑郁症、焦虑症、强迫症(OCD)和其他需要5-HT1激动剂或拮抗剂的疾病中具有用途。
• Diels–Alder reaction of fused pyran-2-ones with ethyl vinyl ether
  作者：Amadej Juranovič、Krištof Kranjc、Slovenko Polanc、Franc Perdih、Marijan Kočevar

  DOI：10.1007/s00706-012-0734-4

  日期：2012.5

  AbstractEthyl vinyl ether was found to be an appropriate synthetic equivalent of acetylene for a set of Diels–Alder reactions with fused pyran-2-ones that yield fused carbocyclic systems. Transformations were conducted under microwave irradiation with DABCO (as a catalyst for the elimination of ethanol) and with n-butanol as the additive. A single-crystal X-ray diffraction structure is presented for

  摘要发现乙基乙烯基醚是乙炔的适当合成当量，适用于与稠合吡喃-2-酮的一系列Diels-Alder反应，产生稠合碳环系统。在微波辐射下，用DABCO（作为消除乙醇的催化剂）和正丁醇作为添加剂进行转化。提出了N-（5,6,7,8-四氢-6-甲基-8-氧代萘-2-基）苯甲酰胺的单晶X射线衍射结构。 图形概要
• Naphthalene derivatives
  申请人：Chenard L. Bertrand

  公开号：US20050080090A1

  公开（公告）日：2005-04-14

  Compounds of the formula (1) where R 1 is of formula (II), (III), or (IV), or (V); R 2 is —R 4 , —O—R 4 , —O—S(O) 2 —R 4 , —NR 4 R 5 , R 4 —(CH 2 ) b —NH(C═X)—(CH 2 )C—, R 4 —(CH 2 ) b —O(C—O)NH—(CH 2 ) c —(C═O)NH—, R 4 —(C═O)NH—(C═O)NH—, —CH 2 ) b —NH(C═X)—(CH 2 ) c —R 4 , R 4 —(CH 2 ) b —O(C═O)CH 2 ) c —, —(CH 2 ) b —O(C═O)—(CH 2 ) c —R 4 , —NH(C═X)NH—R 4 , R 4 —O(C═O)O—, —O(C═O)NH—R 4 , R 4 —O(C═O)NH—, —(CH 2 ) b —(C═O—(CH 2 ) c —R 4 , —NH—S(O) 2 —R 4 , —C(OH)R 4 R 5 , —CH(OH)—R 4 , —(C═O)—NR 4 , —CN, —NO 2 , substituted C 1 to C 6 alkyl, substituted or unsubstituted C 1 to C 6 alkenyl, or substituted or unsubstituted C 1 to C 6 alkynyl, said substituted moieties substituted with a moiety of the formula —R 4 , —R 4 R 5 , —O—R 4 , or —S(O) d —R 4 ; R 3 is hydrogen, C 1 to C 6 alkyl, C 1 to C 6 alkylaryl, or aryl; R 4 and R 5 are each independently (XV), (XVI), (XVII), (XVII) hydrogen, —CF 3 , C 1 to C 6 alkyl, C 1 to C 6 alkylaryl, with the proviso that when R 2 is —R 4 or —OR 4 , R 4 is not hydrogen or C 1 to C 6 alkyl these compounds are useful psychotherapeutics and are potent serotonin (5-HT 1 ) agonists and antagonists and may be used in the treatment of depression, anxiety, eating disorders, obesity, drug abuse, cluster headache, migraine, pain and chronic paroxysmal hemicrania and headache associated with vascular disorders, and other disorders arising from deficient serotonergic neurotransmission. The compounds can also be used as centrally acting antihypertensives and vasodilators.

  化合物的公式（1），其中R1为公式（II），（III），（IV）或（V）的形式；R2为-R4，-O-R4，-O-S（O）2-R4，-NR4R5，R4-（CH2）b-NH（C═X）-（ ）c-，R4-（ ）b-O（C-O）NH-（ ）c-（C═O）NH-，R4-（C═O）NH-（C═O）NH-，- ）b-NH（C═X）-（ ）c-R4，R4-（ ）b-O（C═O） ）c-，-（ ）b-O（C═O）-（ ）c-R4，-NH（C═X）NH-R4，R4-O（C═O）O-，-O（C═O）NH-R4，R4-O（C═O）NH-，-（ ）b-（C═O-（ ）c-R4，-NH-S（O）2-R4，-C（OH）R4R5，-CH（OH）-R4，-（C═O）-NR4，-CN，-NO2，取代的C1到C6烷基，取代的或未取代的C1到C6烯基，或取代的或未取代的C1到C6炔基，所述取代基以公式-R4，-R4R5，-O-R4或-S（O）d-R4为取代基；R3为氢，C1到C6烷基，C1到C6烷基芳基或芳基；R4和R5各自独立为（XV），（XVI），（XVII），（XVII）氢，-CF3，C1到C6烷基，C1到C6烷基芳基，但当R2为-R4或-OR4时，R4不是氢或C1到C6烷基，这些化合物是有用的心理治疗药物，是有效的5-羟色胺（5-HT1）激动剂和拮抗剂，可用于治疗抑郁症，焦虑症，进食障碍，肥胖症，药物滥用，集群头痛，偏头痛，疼痛和慢性阵发性半头痛和与血管障碍相关的头痛以及其他由5-羟色胺能神经递质缺乏引起的疾病。这些化合物也可用作中枢作用的降压药和血管扩张剂。