(2R,4S)-4-{[3,5-bis(trifluoromethyl)benzyl]-(5-iodopyrimidin-2-yl)}amino-2-ethyl-6-methoxy-3,4-dihydro-2H-[1,5]naphthyridine-1-carboxylic acid ethyl ester | 866531-67-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: (2R,4S)-4-{[3,5-bis(trifluoromethyl)benzyl]-(5-iodopyrimidin-2-yl)}amino-2-ethyl-6-methoxy-3,4-dihydro-2H-[1,5]naphthyridine-1-carboxylic acid ethyl ester
• 英文别名: ethyl (2R,4S)-4-[[3,5-bis(trifluoromethyl)phenyl]methyl-(5-iodopyrimidin-2-yl)amino]-2-ethyl-6-methoxy-3,4-dihydro-2H-1,5-naphthyridine-1-carboxylate
• CAS: 866531-67-1
• 化学式: C₂₇H₂₆F₆IN₅O₃
• 分子量: 709.43
• InChiKey: GLBOHOYDKIROOF-CTNGQTDRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.6
• 重原子数：
  42
• 可旋转键数：
  8
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  80.7
• 氢给体数：
  0
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  (2R,4S)-4-{[3,5-bis(trifluoromethyl)benzyl]-(5-iodopyrimidin-2-yl)}amino-2-ethyl-6-methoxy-3,4-dihydro-2H-[1,5]naphthyridine-1-carboxylic acid ethyl ester 、 巯基乙酸甲酯 在 copper(l) iodide 、 potassium carbonate 、 乙二醇 作用下， 以 异丙醇 为溶剂， 生成
  参考文献：
  名称：

  [EN] TETRAHYDRONAPHTHYRIDINE DERIVATIVES AS CHOLESTERYL ESTER TRANSFER PROTEIN INHIBITORS
  [FR] DERIVES DE TETRAHYDRONAPHTYRIDINE ET PROCEDE D'ELABORATION DESDITS DERIVES

  摘要：

  公开号：

  WO2005095395A3

文献信息

• Tetrahydronaphthyridine derivatives and a process for preparing the same
  申请人：Kubota Hitoshi

  公开号：US20070032485A1

  公开（公告）日：2007-02-08

  A novel compound of the formula (I): wherein R 1 is alkoxycarbonyl or the like, R 2 is alkyl or the like; R 3 is hydrogen or the like; R 4 is alkylene or the like; R 5 is optionally substituted heterocyclic group; R 6 , R 7 , and R 8 are independently hydrogen; alky, alkoxy, or the like; R 10 is optionally substituted aromatic ring, or the like; or a pharmaceutically acceptable salt thereof, which has an inhibitory activity against cholesteryl ester transfer protein (CETP).

  一种化合物的公式（I）：其中R1为烷氧羰基或类似物，R2为烷基或类似物；R3为氢或类似物；R4为烷基或类似物；R5为可选取代的杂环基；R6、R7和R8分别为氢、烷基、烷氧基或类似物；R10为可选取代的芳香环或类似物；或其药学上可接受的盐，该化合物具有对胆固醇酯转移蛋白（CETP）的抑制活性。
• METHOD FOR PREPARING 5-[2-(METHYLTHIO)ETHOXY]PYRIMIDINE-2-AMINE
  申请人：Yamazaki Koichi

  公开号：US20110166351A1

  公开（公告）日：2011-07-07

  A novel method for preparing 5-[2-(methylthio)ethoxy]pyrimidin-2-amine useful as a regent or raw material for manufacture of medicaments, agricultural chemicals, and industrial products, which comprises alkanoylating the amino group of a 2-amino-4-alkoxypyrimidine, then converting the resultant into a 4-hydroxypyrimidine compound by a treatment with anhydrous aluminum chloride, further etherifying the 4-hydroxypyrimidine compound by a reaction with a 2-haloethyl methyl sulfide in the presence of a base, and removing the alkanoyl group to obtain 5-[2-(methylthio)ethoxy]pyrimidin-2-amine.

  一种制备5-[2-(甲硫基)乙氧基]嘧啶-2-胺的新方法，该方法可用于制造药物、农业化学品和工业产品的试剂或原料。该方法包括将2-氨基-4-烷氧基嘧啶的氨基基团进行烷酰化处理，然后通过与无水氯化铝处理将其转化为4-羟基嘧啶化合物，进一步在碱的存在下通过与2-卤代乙基甲硫醚反应将4-羟基嘧啶化合物进行醚化，最后去除烷酰基以获得5-[2-(甲硫基)乙氧基]嘧啶-2-胺。
• US7781443B2
  申请人：——

  公开号：US7781443B2

  公开（公告）日：2010-08-24