四氢酞酰亚胺 | 52169-61-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 中文名称: 四氢酞酰亚胺
• 英文名称: tetrahydrophthalimide
• 英文别名: 3a,4,5,7a-Tetrahydro-1H-isoindole-1,3(2H)-dione；3a,4,5,7a-tetrahydroisoindole-1,3-dione
• CAS: 52169-61-6
• 化学式: C₈H₉NO₂
• 分子量: 151.165
• InChiKey: SPAMRUYRVYMHPV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 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：

  四氢酞酰亚胺 在 potassium osmate(VI) 、 N-甲基吗啉氧化物 作用下， 以 水 、 丙酮 为溶剂， 以79%的产率得到5,6-dihydroxy-hexahydro-isoindole-1,3-dione
  参考文献：
  名称：

  [EN] [C]-FUSED BICYCLIC PROLINE DERIVATIVES AND THEIR USE FOR TREATING ARTHRITIC CONDITIONS
  [FR] DERIVES DE PROLINE BICYCLIQUES 20041028US2003008861A1LIN LINUS S [US], et al20030109example 10, step C example 11, step A example 29, step c (starting material)X2,8XBERGMEIER S C ET AL: "Synthesis of Bicyclic Proline Analogs Using a Formal [3 + 2] Intramolecular Aziridine-Allylsilane Cycloaddition Reaction", TETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, vol. 55, no. 26, 25 June 1999 (1999-06-25), pages 8025 - 8038, XP004168571, ISSN: 0040-4020BERGMEIER S C ET ALSynthesis of Bicyclic Proline Analogs Using a Formal [3 + 2] Intramolecular Aziridine-Allylsilane Cycloaddition ReactionTETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL1999062555260040-40208025803845Scheme 7X2XDATABASE BEILSTEIN BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002288925, Database accession no. BRN:388906BEILSTEINBEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DEBRN:388906AX4XMURAYAMA ET AL, YAKUGAKU ZASSHI, vol. 85, 1965, pages 765 - 769MURAYAMA ET ALYAKUGAKU ZASSHI196585765769WO0027808A1AVENTIS PHARMA GMBH [DE]20000518214814211517A1-9AWO03074048A1WARNER LAMBERT CO [US], et al2003091235253626PX1-9PXOTHMAN M ET AL: "New Fused Lactones from Indolizinediones via N-Acyliminium Ions", TETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, vol. 54, no. 30, 23 July 1998 (1998-07-23), pages 8737 - 8744, XP004124041, ISSN: 0040-4020OTHMAN M ET ALNew Fused Lactones from Indolizinediones via N-Acyliminium IonsTETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL1998072354300040-4020873787443A-EScheme 1X1XGUILLERM G ET AL: "Synthesis of Hydroxylated Pyrrolidines Derivatives as Potential Inhibitors of SAH/MTA Nucleosidase", TETRAHEDRON LETTERS, vol. 28, no. 5, 1987, pages 535 - 538, XP002288924GUILLERM G ET ALSynthesis of Hydroxylated Pyrrolidines Derivatives as Potential Inhibitors of SAH/MTA NucleosidaseTETRAHEDRON LETTERS19872855355384AScheme 2X1X

  摘要：

  本发明涉及一种[c]-融合的双环脯氨酸衍生物，或其药用可接受的盐；包括该化合物或其盐的药物组合物；以及治疗疾病的方法，包括但不限于预防或抑制关节软骨损伤，以及预防或治疗以关节软骨损伤、关节炎或关节疼痛为特征的疾病的方法。[c]-融合的双环脯氨酸衍生物是如上所述的I式化合物。以关节软骨损伤或关节疼痛为特征的疾病包括，例如，骨关节炎和类风湿性关节炎。类风湿性关节炎还以关节炎为特征。本发明还涉及合成和制备[c]-融合的双环脯氨酸衍生物或其药用可接受的盐的方法。

  公开号：

  WO2004092134A1
• 作为产物：
  描述：

  3,4,5,6-四氢苯酐 生成 四氢酞酰亚胺
  参考文献：
  名称：

  Phosphorus containing 1-cyclohexene-1,2-dicarboxamides

  摘要：

  1-环己烯-1,2-二甲酰胺的替代物、其合成方法、其中间体以及所述化合物用于控制杂草的用途。

  公开号：

  US04613675A1

文献信息

• [EN] SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE<br/>[FR] COMPOSÉS HÉTÉROARYLE SUBSTITUÉS ET LEURS MÉTHODES D'UTILISATION
  申请人：CALITOR SCIENCES LLC

  公开号：WO2015148868A1

  公开（公告）日：2015-10-01

  The present invention provides novel heteroaryl compounds, pharmaceutical acceptable salts and formulations thereof useful in preventing, treating or lessening the severity of a protein-mediated disease. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of protein kinase-mediated disease.

  本发明提供了新颖的杂环芳基化合物，其药用盐和制剂，在预防、治疗或减轻蛋白介导的疾病的严重程度方面具有用处。该发明还提供了包括这些化合物的药用组合物以及使用这些组合物治疗蛋白激酶介导的疾病的方法。
• [EN] CONDENSED PIPERIDINE COMPOUNDS ACTING AS ADRENERGIC RECEPTOR ANTAGONISTS USEFUL IN THE TREATMENT OF PROSTATIC HYPERPLASIA AND LOWER URINARY SYMPTOMS<br/>[FR] COMPOSES A BASE DE PIPERIDINES CONDENSES AGISSANT COMME ANTAGONISTES DES RECEPTEURS ADRENERGIQUES, UTILISES DANS LE TRAITEMENT DES SYMPTOMES LIES A L'HYPERPLASIE BENIGNE DE LA PROSTATE ET AUX VOIES URINAIRES INFERIEURES
  申请人：RANBAXY LAB LTD

  公开号：WO2005118591A1

  公开（公告）日：2005-12-15

  The present invention relates to α1a and/or α1d adrenergic receptor antagonists. Compounds provided herein can function as α1a and/or α1d adrenergic receptor antagonist and can be used for the treatment of a disease or disorder mediated through α1a and/or α1d adrenergic receptor. Compounds provided herein can be used for the treatment of benign prostatic hyperplasia (BPH) and the related symptoms thereof, lower urinary tract symptoms (LUTS) associated with or without BPH. Processes for the preparation of the provided compounds, as well as, pharmaceutical composition containing the provided compounds, and methods of treating benign prostatic hyperplasia or related symptoms thereof are provided herein.

  本发明涉及α1a和/或α1d肾上腺素受体拮抗剂。本文提供的化合物可以作为α1a和/或α1d肾上腺素受体拮抗剂发挥作用，并可用于治疗通过α1a和/或α1d肾上腺素受体介导的疾病或紊乱。本文提供的化合物可用于治疗良性前列腺增生（BPH）及其相关症状，与或不伴有BPH的下尿路症状（LUTS）。本文提供了所述化合物的制备方法，以及含有所述化合物的药物组合物，以及治疗良性前列腺增生或相关症状的方法。
• [EN] COMPOSITIONS, DOSAGE FORMS, AND COADMINISTRATION OF AN OPIOID AGONIST COMPOUND AND AN ANALGESIC COMPOUND<br/>[FR] COMPOSITIONS, FORMES GALÉNIQUES ET COADMINISTRATION D'UN COMPOSÉ AGONISTE OPIOÏDE ET D'UN COMPOSÉ ANALGÉSIQUE
  申请人：NEKTAR THERAPEUTICS

  公开号：WO2013070617A1

  公开（公告）日：2013-05-16

  The present invention relates generally to the co-administration of an opioid agonist compound and an analgesic compound. In addition, the invention relates to, among other things, dosage forms for co-administration of an opioid agonist compound and an analgesic compound, methods for administering an opioid agonist compound and an analgesic compound, compositions comprising an opioid agonist compound and an analgesic compound, dosage forms comprising an opioid agonist compound and an analgesic compound, and so on.

  本发明一般涉及阿片受体激动剂化合物和镇痛化合物的联合给药。此外，该发明涉及阿片受体激动剂化合物和镇痛化合物的联合给药的剂型，给药阿片受体激动剂化合物和镇痛化合物的方法，包含阿片受体激动剂化合物和镇痛化合物的组合物，包含阿片受体激动剂化合物和镇痛化合物的剂型等。
• [EN] SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE<br/>[FR] COMPOSÉS HÉTÉROARYLES SUBSTITUÉS ET MÉTHODES D'UTILISATION
  申请人：CALITOR SCIENCES LLC

  公开号：WO2015094803A1

  公开（公告）日：2015-06-25

  The present invention provides new heteroaryl compounds, pharmaceutical acceptable salts and formulations thereof useful in preventing, treating or lessening the severity of JAK-mediated diseases. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of JAK-mediated diseases.

  本发明提供了新的杂环芳基化合物，其药用盐和制剂在预防、治疗或减轻JAK介导疾病的严重程度方面具有用处。该发明还提供了包括这些化合物的药用组合物以及使用这些组合物治疗JAK介导疾病的方法。
• [EN] PROCESS FOR PREPARATION OF DERIVATIVES OF TETRAHYDROPHTHALIMIDE<br/>[FR] PROCÉDÉ DE PRÉPARATION DE DÉRIVÉS DE TÉTRAHYDROPHTALIMIDE
  申请人：RALLIS INDIA LTD

  公开号：WO2014122674A1

  公开（公告）日：2014-08-14

  The present disclosure provides a process for preparation of a compound of formula 1, or isomers or its derivatives thereof, which show a high herbicidal activity against wide variety of weeds. (I) wherein R1 is a C3-C4 alkynyl group, a C1-C5 alkyl group, or a C3-C4 alkenyl group, and X is selected from the group consisting of F, Cl, Br, I or H atom.

  本公开提供了一种制备化合物的过程，该化合物的化学式为1，或其异构体或衍生物，对各种杂草表现出高除草活性。(I)其中R1是C3-C4炔基，C1-C5烷基或C3-C4烯基，X选自F、Cl、Br、I或H原子组成的组。