2-amino-5-dimethylaminomethylthiazole | 948572-68-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-amino-5-dimethylaminomethylthiazole
• 英文别名: 5-[(Dimethylamino)methyl]-1,3-thiazol-2-amine
• CAS: 948572-68-7
• 化学式: C₆H₁₁N₃S
• 分子量: 157.239
• InChiKey: XWRQHPFDMUNUQU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  70.4
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  tert-butyl N-[5-(dimethylaminomethyl)thiazol-2-yl]carbamate 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 6.0h， 生成 2-amino-5-dimethylaminomethylthiazole
  参考文献：
  名称：

  WO2007/99326

  摘要：

  公开号：

文献信息

• [EN] THIAZOLE COMPOUNDS FOR THE TREATMENT OF NEURODEGENERATIVE DISORDERS<br/>[FR] COMPOSES THIAZOLE UTILES POUR LE TRAITEMENT DES MALADIES NEURODEGENERATIVES
  申请人：PFIZER PROD INC

  公开号：WO2004033439A1

  公开（公告）日：2004-04-22

  The invention provides compounds of Formula (I): wherein R1, R2, R3, R4, R6, R7, and A are as defined. Compounds of Formula (I) have activity inhibiting production of Aß-peptide. The invention also provides pharmaceutical compositions and methods for treating diseases, for example Alzheimer's disease, in mammals comprising compounds of Formula (I).

  该发明提供了Formula (I)的化合物：其中R1、R2、R3、R4、R6、R7和A的定义如上所述。Formula (I)的化合物具有抑制Aß-肽产生活性。该发明还提供了包括Formula (I)的化合物的药物组合物和治疗方法，用于治疗哺乳动物的疾病，例如阿尔茨海默病。
• Thiazole compounds for treatment of neurodegenerative disorders
  申请人：Pfizer Inc

  公开号：US20040152747A1

  公开（公告）日：2004-08-05

  The invention provides compounds of Formula I: 1 wherein R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , and A are as defined. Compounds of Formula I have activity inhibiting production of A&bgr;-peptide. The invention also provides pharmaceutical compositions and methods for treating diseases, for example Alzheimer's disease, in mammals comprising compounds of Formula I.

  本发明提供了I式化合物：1其中R1、R2、R3、R4、R6、R7和A的定义如上。I式化合物具有抑制Aβ肽生产的活性。本发明还提供了包含I式化合物的制药组合物和治疗哺乳动物疾病的方法，例如阿尔茨海默病。
• Novel 2-pyridinecarboxamide derivatives
  申请人：Mitsuya Morihiro

  公开号：US20060258701A1

  公开（公告）日：2006-11-16

  The present invention relates to a compound which has a glucokinase-activating effect and is useful as a therapeutic agent for diabetes mellitus, being represented by a formula (I): [wherein X 1 represents a nitrogen atom, sulfur atom, oxygen atom or the like; R 1 represents a 6- to 10-membered aryl group, 5- to 7-membered heteroaryl group or the like; D represents an oxygen atom or sulfur atom; R and R 3 are the same or different, each representing a hydrogen atom, lower alkyl group or the like; a formula (II) represents an optionally substituted 5- to 7-membered heteroaryl group or the like; a formula (III) represents a monocyclic or bicyclic heteroaryl group] or a pharmaceutically acceptable salt thereof.

  本发明涉及一种化合物，具有激活葡萄糖激酶的效果，并可用作糖尿病治疗剂，其化学式表示为（I）：[其中X1表示氮原子、硫原子、氧原子或类似物；R1表示6-至10-成员芳基基团、5-至7-成员杂芳基基团或类似物；D表示氧原子或硫原子；R和R3相同或不同，分别表示氢原子、低碳基或类似物；式（II）表示可选取代的5-至7-成员杂芳基团或类似物；式（III）表示单环或双环杂芳基团]或其药学上可接受的盐。
• QUINOLINE DERIVATIVES
  申请人：Jung Frederic Henri

  公开号：US20090076074A1

  公开（公告）日：2009-03-19

  The invention concerns quinoline derivatives of Formula I or a pharmaceutically-acceptable salt thereof, wherein each of X 1 , p, R 1 , q, R 2 , R 3 , R 4 , R 5 , Ring A, r and R 6 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.

  本发明涉及公式I的喹啉衍生物或其药学上可接受的盐，其中X1、p、R1、q、R2、R3、R4、R5、环A、r和R6中的每一个具有在本说明书中定义的任何含义；制备它们的过程，包含它们的制药组合物以及它们在制造用于治疗细胞增殖性疾病的药物的过程中的使用。
• RHO KINASE INHIBITORS
  申请人：Dahmann Georg

  公开号：US20100041645A1

  公开（公告）日：2010-02-18

  Substituted amide and urea derivatives useful as inhibitors of Rho kinase are described, which inhibitors can be useful in the treatment of various disorders such as cardiovascular diseases, cancer, neurological diseases, renal diseases, bronchial asthma, erectile dysfunction and glaucoma.

  本文介绍了一种替代酰胺和脲衍生物，这些衍生物可用作Rho激酶的抑制剂，在治疗心血管疾病、癌症、神经系统疾病、肾脏疾病、支气管哮喘、勃起功能障碍和青光眼等各种疾病中有用。