[(chlorocarbonyl)oxy]methyl 2-methylpropanoate | 353736-67-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机碳酸及其衍生物
• 英文名称: [(chlorocarbonyl)oxy]methyl 2-methylpropanoate
• 英文别名: carbonochloridoyloxymethyl 2-methylpropanoate
• CAS: 353736-67-1
• 化学式: C₆H₉ClO₄
• 分子量: 180.588
• InChiKey: JOWSLMCIDSDGEG-UHFFFAOYSA-N

物化性质

• 沸点：
  192.5±23.0 °C(Predicted)
• 密度：
  1.234±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  11
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  [(chlorocarbonyl)oxy]methyl 2-methylpropanoate 、 (4S,5S)-5-((2S)-2-{[(3-amino-2,2-dimethyl-3-oxopropyl)amino]carbonyl}-3-methylbutyl)-4-{(2S)-2-[4-methoxy-3-(3-methoxypropoxy)benzyl]-3-methylbutyl}-1,3-oxazolidine 在 4-二甲氨基吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 生成 1-(isobutyryloxy)methyl (4S,5S)-5-[(S)-2-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-3-methylbutyl]-4-{(S)-2-[4-methoxy-3-(3-methoxypropoxy)benzyl]-3-methylbutyl}oxazolidine-3-carboxylate
  参考文献：
  名称：

  [EN] NOVEL 1,3-OXAZOLIDINE COMPOUNDS AND THEIR USE AS RENIN INHIBITORS
  [FR] NOUVEAUX COMPOSÉS DE 1,3-OXAZOLIDINE ET UTILISATION DE CES DERNIERS COMME INHIBITEURS DE LA RÉNINE

  摘要：

  本发明涉及某些新颖的1,3-噁唑烷化合物（I）的公式，以及制备这类化合物的方法，以及它们作为肾素抑制剂或肾素抑制剂的前药的用途。

  公开号：

  WO2011056126A1
• 作为产物：
  描述：

  (((ethylthio)carbonyl)oxy)methyl isobutyrate 生成 [(chlorocarbonyl)oxy]methyl 2-methylpropanoate
  参考文献：
  名称：

  AMINO TRICYCLIC-NUCLEOSIDE COMPOUNDS, COMPOSITIONS, AND METHODS OF USE

  摘要：

  提供的是式（I）的化合物或其药用可接受的盐或溶剂化合物。这些化合物和组合物对治疗由黄病毒科病毒引起的病毒感染有用。

  公开号：

  US20090062223A1

文献信息

• [EN] ACYLOXYMETHYLCARBAMATE PRODRUGS OF OXAZOLIDINONES<br/>[FR] BIOPRECURSEURS ACYLOXYMETHYLCARBAMATE DES OXAZOLIDINONES
  申请人：UPJOHN CO

  公开号：WO2005028473A1

  公开（公告）日：2005-03-31

  The present invention relates to acyloxymethylcarbamate oxazolidinones. The compounds of the present invention have potent activity with excellent oral bioavailability against Gram-positive and Gram-negative bacteria.

  本发明涉及酰氧甲基氨基甲酸酯噁唑烷酮。本发明的化合物具有优良的口服生物利用度，对革兰氏阳性和阴性细菌具有强效活性。
• 9-Aminocarbonylsubstituted derivatives of glycylcyclines
  申请人：Sum Phaik-Eng

  公开号：US20070049564A1

  公开（公告）日：2007-03-01

  This invention provides compounds of Formula I having the structure where R 1 , R 2 , R 3 and A are defined in the specification or a pharmaceutically acceptable salt thereof useful as antibacterial agents. Compounds according to Formula (II): where Q, R 4 , R 5 , R 6 and R 10 and A are defined in the specification are useful as chemical intermediates.

  这项发明提供了具有结构的化合物，其中R1、R2、R3和A在规范中定义，或其药用盐，可用作抗菌剂。根据公式（II）的化合物： 其中Q、R4、R5、R6和R10以及A在规范中定义，可用作化学中间体。
• Acyloxymethylcarbamate prodrugs of oxazolidinones
  申请人：Josyula Venkata Nagendra Vara Prasad

  公开号：US20050267104A1

  公开（公告）日：2005-12-01

  The present invention relates to acyloxymethylcarbamate oxazolidinones. The compounds of the present invention have potent activity with excellent oral bioavailability against Gram-positive and Gram-negative bacteria.

  本发明涉及酰氧甲基氨基甲酸酯噁唑烷酮。本发明的化合物具有强大的活性和良好的口服生物利用度，对革兰氏阳性和革兰氏阴性细菌具有优异的抗菌活性。
• Enhanced propertied pesticides
  申请人：Rohm and Haas Company

  公开号：US06376548B1

  公开（公告）日：2002-04-23

  This invention relates to enhanced propertied pesticides which can be used as fungicides, herbicides, insecticides, rodenticides or biocides, compositions comprising enhanced propertied pesticides, and the method of use of enhanced propertied pesticides and their compositions. It has been found that certain pesticidal compounds can be substituted with a moiety which comprises a substituent which enhances or changes the properties of the pesticidal compound. Additionally, some of the compounds of this invention may comprise two pesticidal components which can be different from one another. The invention relates also to pesticidal compositions comprising a pesticidal compound of this invention and an pesticidally acceptable carrier as well as methods of controlling a pest comprising applying a pesticidally effective amount of a composition comprising a compound of this invention and a pesticidally acceptable carrier to the pest, to the locus of the pest or to the growth medium of said pest.

  本发明涉及增强性能杀虫剂，可用作杀菌剂、除草剂、杀虫剂、杀鼠剂或生物杀剂，以及包含增强性能杀虫剂的组合物和增强性能杀虫剂及其组合物的使用方法。发现某些杀虫化合物可用含有增强或改变杀虫化合物性质的取代基的基团替代。此外，本发明的某些化合物可能包含两种不同的杀虫成分。本发明还涉及包含本发明中的杀虫化合物和杀虫剂可接受的载体的杀虫剂组合物，以及控制害虫的方法，包括将本发明中的化合物和杀虫剂可接受的载体的杀虫剂组合物的有效量施用于害虫、害虫生长地点或害虫的生长介质。
• Cycloalkyl-Substituted Imidazole Derivative
  申请人：Nagata Tsutomu

  公开号：US20130022587A1

  公开（公告）日：2013-01-24

  A compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof, wherein A represents a C3 to C12 cycloalkyl group which may be substituted by one to three selected from a fluoro group, a hydroxy group, a C1 to C6 alkyl group, etc; R 1 , R 2 , and R 3 each independently represent a hydrogen atom, a fluoro group, or a C1 to C6 alkyl group; R 4 represents a hydrogen atom or a prodrug group; and Y represents —CH 2 —CHR 5 —CH 2 —NHR 6 (wherein R 5 represents a hydrogen atom, a C1 to C6 alkyl group, or a C1 to C6 alkoxy group, and R 6 represents a hydrogen atom or a prodrug group), or the like exhibits excellent TAFIa inhibitory activity and is useful as a therapeutic drug for myocardial infarction, angina pectoris, acute coronary syndrome, cerebral infarction, deep vein thrombosis, pulmonary embolism, and the like.

  以下是通式（I）所代表的化合物或其药学上可接受的盐，其中A代表一个C3到C12的环烷基，该环烷基可以被一个到三个选自氟基、羟基、C1到C6烷基等的基团所取代；R1、R2和R3各自独立地代表氢原子、氟基或C1到C6烷基；R4代表氢原子或前药基团；Y代表—CH2—CHR5— —NHR6（其中R5代表氢原子、C1到C6烷基或C1到C6烷氧基，R6代表氢原子或前药基团）等，具有极好的TAFIa抑制活性，是治疗心肌梗死、心绞痛、急性冠状动脉综合征、脑梗死、深静脉血栓形成、肺栓塞等疾病的治疗药物。