methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate | 1220450-57-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate
• 英文别名: methyl 4-tert-butyl-2-methylsulfanylpyrimidine-5-carboxylate
• CAS: 1220450-57-6
• 化学式: C₁₁H₁₆N₂O₂S
• 分子量: 240.326
• InChiKey: GUMPQILPQJNLGQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  77.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  methyl 3-oxo-2-(iodomethylene)-4,4-dimethylpentanoate 、 S-甲基异硫脲盐酸盐 在 三乙胺 作用下， 以 乙醇 为溶剂， 反应 0.5h， 生成 methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate
  参考文献：
  名称：

  Efficient Assembly of 2,5,6-Substituted Pyrimidines via MgI₂-Mediated Morita−Baylis−Hillman Reaction

  摘要：

  A mild and efficient protocol for the synthesis of a 2,6-disubstituted pyrimidine-5-carboxylate library via a Morita-Baylis-Hillman (MBH) adduct is described. Herein, the three step methodology involves the use of substituted alpha-iodomethylene beta-keto ester intermediates obtained after oxidation of the MBH adducts, which are condensed with various types of amidine or guanidine derivatives, to generate the 2, 6-disubstituted pyrimidines-5-carboxylate libraries.

  DOI：

  10.1021/cc100001e

文献信息

• PYRIMIDINE COMPOUND
  申请人：Matsushima Yuji

  公开号：US20110053912A1

  公开（公告）日：2011-03-03

  A novel and excellent method for preventing and/or treating diseases related to a cannabinoid type 2 receptor, based on an agonistic action on a cannabinoid type 2 receptor. It was found that a hetero ring derivative mainly having two substituents, for example, a pyrimidine-5-carboxamide derivative having a substituent amino group at the 2-position, exhibits a potent agonistic action on a cannabinoid type 2 receptor, and can be an agent for preventing and/or treating diseases related to a cannabinoid type 2 receptor such as inflammatory diseases, pain, and the like.

  一种预防和/或治疗与大麻素2型受体相关疾病的新颖优秀方法，基于对大麻素2型受体的激动作用。发现一种异核环衍生物主要具有两个取代基，例如，在2-位置具有取代基氨基的嘧啶-5-羧酰胺衍生物，表现出对大麻素2型受体的强效激动作用，可以成为预防和/或治疗与大麻素2型受体相关疾病，如炎症性疾病、疼痛等的药物。
• Pyrimidine compound
  申请人：Matsushima Yuji

  公开号：US08524727B2

  公开（公告）日：2013-09-03

  A novel and excellent method for preventing and/or treating diseases related to a cannabinoid type 2 receptor, based on an agonistic action on a cannabinoid type 2 receptor. It was found that a hetero ring derivative mainly having two substituents, for example, a pyrimidine-5-carboxamide derivative having a substituent amino group at the 2-position, exhibits a potent agonistic action on a cannabinoid type 2 receptor, and can be an agent for preventing and/or treating diseases related to a cannabinoid type 2 receptor such as inflammatory diseases, pain, and the like.

  一种预防和/或治疗与大麻素2型受体相关的疾病的新颖和优秀方法，基于对大麻素2型受体的激动作用。发现一种异环衍生物主要具有两个取代基，例如，在2位具有取代氨基的嘧啶-5-羧酰胺衍生物表现出对大麻素2型受体的强效激动作用，并可作为预防和/或治疗与大麻素2型受体相关的疾病的药物，例如炎症性疾病、疼痛等。
• US8524727B2
  申请人：——

  公开号：US8524727B2

  公开（公告）日：2013-09-03
• Efficient Assembly of 2,5,6-Substituted Pyrimidines via MgI₂-Mediated Morita−Baylis−Hillman Reaction
  作者：Vasudha Sharma、Mark L. McLaughlin

  DOI：10.1021/cc100001e

  日期：2010.5.10

  A mild and efficient protocol for the synthesis of a 2,6-disubstituted pyrimidine-5-carboxylate library via a Morita-Baylis-Hillman (MBH) adduct is described. Herein, the three step methodology involves the use of substituted alpha-iodomethylene beta-keto ester intermediates obtained after oxidation of the MBH adducts, which are condensed with various types of amidine or guanidine derivatives, to generate the 2, 6-disubstituted pyrimidines-5-carboxylate libraries.