7-(2',2',2'-trifluoroethylaminocarbonyl)-2,4-(1H,3H,5H)-(1)-benzopyrano-(2,3-d)-pyrimidinedione | 74914-26-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡喃吡啶类
• 英文名称: 7-(2',2',2'-trifluoroethylaminocarbonyl)-2,4-(1H,3H,5H)-(1)-benzopyrano-(2,3-d)-pyrimidinedione
• 英文别名: 2,4-dioxo-N-(2,2,2-trifluoroethyl)-1,5-dihydrochromeno[2,3-d]pyrimidine-7-carboxamide
• CAS: 74914-26-4
• 化学式: C₁₄H₁₀F₃N₃O₄
• 分子量: 341.246
• InChiKey: RUGFTSQAGRRACM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  96.5
• 氢给体数：
  3
• 氢受体数：
  7

文献信息

• Benzopyrano derivatives, pharmaceutical compositions containing them and processes for preparing the compounds and compositions
  申请人：Technobiotic Ltd.

  公开号：EP0008277A1

  公开（公告）日：1980-02-20

  Novel compounds of the formula wherein each of R3 and R5 represents hydrogen or loweralkyl, n Is an integer from one to four and R represents hydrogen, ' loweralkyl, lowercycloalkyl, lowercycloalkyl-loweralkyl, acyloxyloweralkyl, hydroxyloweralkyl, lower-alkoxyloweralkyl, nitro, halogeno, haloloweralkyl, hydroxy, loweralkoxy, acylaminoloweralkyl, aminoloweralkyl, mono- or diloweralkylaminoloweralkyl, alkanoyloxy, carboxy, loweralkoxycarbonyl, acyl, formyl, cyano or a carboxamido moiety of the structure wherein A is straight or branched chain alkyl with up to 12 carbon atoms, lowercycloalkyl, lowercycloalkylloweralkyl, loweralkoxyloweralkyl, hydroxyloweralkyl, fluoroloweralkyl, loweralkenyl, loweralkylthioloweralkyl, loweralkylsulfoxyloweralkyl, loweralkylsulfonylloweralkyl, thiazolyt, oxazolyl, thiadiazolyl, methylthiadiazolyl, furyl, pyrazolyl, tetrazolyl, methyltetrazolyl, hydroxypyrimidinyl, phenyl, pyrimidinyl-dione, or the grouping wherein E is a straight or branched chain or cyclic loweralkylene, x is zero or one and Q is hydroxy, loweralkoxy, amino or mono- or diloweralkylamino; or the grouping -E-Re, wherein E is as defined above and is optionally substituted by hydroxy and/or phenyl, R8 is phenyl, thiazolyl, oxazolyl, thiadiazolyl, methylthiadiazolyl, tetrazolyl, methyltetrazolyl, furyl, pyridiyl, methylpyridiyl or piperidinyl; and B is hydrogen, loweralkyl, lowercycloalkyl, lowercycioalkylioweralkyl, or loweralkenyl; or A and B, when taken together with the nitrogen atom to which they are attached, represent imidazolyl, morpholinyl, pyrrolidinyl, piperidinyl or piperazinyl said heterocyclic rings being optionally substituted by hydroxy, loweralkyl or hydroxyloweralkyl; and pharmaceutically acceptable salts thereof. The preparation of these compounds by five methods is described, in particular one inventive method which comprises reacting a correspondingly R-substituted salicylaldehyde and barbituric acid in an alcoholic solvent in the presence of a sulfonic acid. Representative compounds of the invention have been shown to exhibit anti-allergy reactions and are thus useful in treating, such diseases as asthma, allergic rhinitis, urticaria and ulcerative colitis.

  式中的新型化合物 其中 R3 和 R5 各自代表氢或低级烷基，n 是 1 至 4 的整数，R 代表氢、'低级烷基、低级环烷基、低级环烷基-低级烷基、酰氧基低级烷基、羟基低级烷基、低级烷氧基低级烷基、硝基、卤素、卤代低级烷基、羟基、低级烷氧基、酰基氨基低级烷基、氨基低级烷基、单烷基或稀释低级烷基氨基低级烷基、烷酰氧基、羧基、低级烷氧基羰基、酰基、甲酰基、氰基或结构为羧酰胺的分子 其中 A 是碳原子数不超过 12 个的直链或支链烷基、低级环烷基、低级环烷氧基低级烷基、低级烷氧基低级烷基、羟基低级烷基、氟代低级烷基、低级烯基、低级烷硫基低级烷基、噻唑基、噁唑基、噻二唑基、甲硫二唑基、呋喃基、吡唑基、四唑基、甲基四唑基、羟基嘧啶基、苯基、嘧啶基二酮或以下基团 其中 E 为直链或支链或环状低级烯烃，x 为 0 或 1，Q 为羟基、低级烷氧基、氨基或单或稀烷基氨基；或基团-E-Re，其中 E 如上文所定义并可选被羟基和/或苯基取代，R8 为苯基、噻唑基、噁唑基、噻二唑基、甲硫二唑基、四唑基、甲基四唑基、呋喃基、吡啶基、甲基吡啶基或哌啶基；而 B 是氢、低级烷基、低级环烷基、低级环烷基低级烷基或低级烯基；或者 A 和 B 连同它们所连接的氮原子代表咪唑基、吗啉基、吡咯烷基、哌啶基或哌嗪基，所述杂环可任选被羟基、低级烷基或羟基低级烷基取代；以及它们的药学上可接受的盐。 本发明描述了通过五种方法制备这些化合物的方法，特别是一种创造性的方法，该方法包括在磺酸存在下，在醇溶剂中使相应的 R 取代水杨醛和巴比妥酸反应。本发明的代表性化合物已被证明具有抗过敏反应，因此可用于治疗哮喘、过敏性鼻炎、荨麻疹和溃疡性结肠炎等疾病。
• US4272535A
  申请人：——

  公开号：US4272535A

  公开（公告）日：1981-06-09