1-(2-Methylpropoxy)propan-1-ol | 34330-54-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(2-Methylpropoxy)propan-1-ol
• CAS: 34330-54-6；26447-43-8
• 化学式: C₇H₁₆O₂
• 分子量: 132.2
• InChiKey: RVKCEMGSOAGADA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  9
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• HEXAHYDRODIAZEPINOQUINOLINES CARRYING A CYCLIC RADICAL
  申请人：AbbVie Deutschland GmbH & Co. KG

  公开号：US20150259343A1

  公开（公告）日：2015-09-17

  The present invention relates to tricyclic hexahydrodiazepinoquinolines carrying a cyclic substituent, to a method for producing them, to a pharmaceutical composition containing such compounds, to their use as modulators, especially agonists or partial agonists, of the 5-HT 2C receptor, their use for preparing a medicament for the prevention or treatment of conditions and disorders which respond to the modulation of 5-HT 2C receptor, to a method for preventing or treating conditions and disorders which respond to the modulation of 5-HT 2C receptor, and processes for preparing such compounds and compositions.

  本发明涉及携带环状取代基的三环六氢二氮杂喹啉类化合物，以及生产它们的方法，含有这类化合物的药物组合物，它们作为5-HT2C受体的调节剂，特别是激动剂或部分激动剂的用途，用于制备用于预防或治疗对5-HT2C受体调节产生反应的疾病和疾病的药物，用于预防或治疗对5-HT2C受体调节产生反应的疾病和疾病的方法，以及制备这类化合物和组合物的方法。
• [EN] PROCESS FOR OBTAINING (S)-2-BENZYL-4-((3AR,7AS)-HEXAHYDRO-1 H-ISOINDOL- 2(3H)-YL)-4-OXOBUTANOIC ACID AND SALTS THEREOF<br/>[FR] PROCÉDÉ POUR L'OBTENTION D'ACIDE (S)-2-BENZYL-4-((3AR,7AS)-HEXAHYDRO-1H-ISOINDOL-2(3H)-YL)-4-OXOBUTANOÏQUE ET DE SELS DE CELUI-CI
  申请人：LESVI LABORATORIOS SL

  公开号：WO2013189829A1

  公开（公告）日：2013-12-27

  Comprising reacting compound (IV) with compound (V) in a solvent to give (S)-mitiglinide (II) and compound (III) as a by- product; removing the solvent and adding ethyl acetate to precipitate compound (III); collecting the solid and applying at least one cycle process comprising: - refluxing the solution of compound (III) with an organic solvent to give (S)-mitiglinide (II) and further compound (III) as a by-product, - removing the organic solvent and adding ethyl acetate to precipitate compound (III); and - separating the mother liquors from the solid, and mixing all the mother liquors; removing the ethyl acetate from the mother liquors to obtain (S)-mitiglinide.

  将化合物（IV）与化合物（V）在溶剂中反应，得到（S）-米格林肽（II）和化合物（III）作为副产物；去除溶剂并加入乙酸乙酯以沉淀化合物（III）；收集固体并应用至少一个循环过程，包括：- 用有机溶剂回流化合物（III）的溶液，得到（S）-米格林肽（II）和进一步的化合物（III）作为副产物，- 去除有机溶剂并加入乙酸乙酯以沉淀化合物（III）；- 将母液与固体分离，并混合所有母液；从母液中去除乙酸乙酯以获得（S）-米格林肽。
• PREPARATION OF DIHYDROPYRIDINES
  申请人：VISHNU NEWADKAR RAVINDRANATH

  公开号：US20110275825A1

  公开（公告）日：2011-11-10

  The invention relates to a method and compounds for the preparation of clevidipine butyrate, a very short acting hypertensive calcium antagonist, as well as the synthesis of these compounds useful for the preparation of clevidipine (also known as clevidipine butyrate). Moreover the invention also discloses polymorphic forms of clevidipine butyrate, useful for the preparation of pharmaceutical compositions, and processes to prepare them.

  该发明涉及一种用于制备克莱维地平丁酸酯的方法和化合物，克莱维地平丁酸酯是一种作用时间非常短的高血压钙拮抗剂，以及用于制备克莱维地平（也称为克莱维地平丁酸酯）的这些化合物的合成。此外，该发明还揭示了克莱维地平丁酸酯的多态形式，用于制备药物组合物，并揭示了用于制备这些多态形式的方法。
• [EN] BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES<br/>[FR] COMPOSÉS BENZAMIDE ET LEUR UTILISATION EN TANT QU'HERBICIDES
  申请人：BASF SE

  公开号：WO2019162308A1

  公开（公告）日：2019-08-29

  The present invention relates to benzamide compounds of formula (I) wherein the variables are defined as in the claims and the description, the N-oxides and salts thereof, and to compositions comprising the same. The invention also relates to the use of the benzamide compounds or of the compositions comprising such compounds for controlling unwanted vegetation, and to a method for controlling unwanted vegetation by applying said compounds or compositions.

  本发明涉及式（I）的苯甲酰胺化合物，其中变量如权利要求和说明书中所定义，其N-氧化物和盐，以及包含它们的组合物。本发明还涉及使用苯甲酰胺化合物或包含这种化合物的组合物来控制不良植被，以及通过应用该化合物或组合物来控制不良植被的方法。
• [EN] PROCESS FOR PREPARING PRASUGREL<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION DE PRASUGREL
  申请人：LESVI LABORATORIOS SL

  公开号：WO2013014295A1

  公开（公告）日：2013-01-31

  The present invention is directed to an improved process for preparing, prasugrel and maleate salt of Prasugrel and, optionally other pharmaceutically acceptable salts from, prasugrel and said maleate salt, in high yields and purity, which can be used at industrial scale. The process of the present invention comprises the steps of bromination, condensation, acetylating and optionally converting into maleate salt and, if desired, conversion into another pharmaceutically acceptable salt from it. The present process is advantageous in terms of productivity, efficacy, purity and also prevents the use of toxic substances.

  本发明涉及一种改进的制备过程，用于从prasugrel和prasugrel的maleate盐，以及可选地从prasugrel和该maleate盐中制备其他药用盐，高产率和纯度中制备，可用于工业规模。本发明的过程包括溴化、缩合、乙酰化以及可选地转化为maleate盐，并如有需要，从中转化为另一种药用盐。本过程在生产效率、功效、纯度方面具有优势，并且还能防止使用有毒物质。