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3,5-dimethoxypyrazine-2-carboxylic acid | 1286756-62-4

中文名称
——
中文别名
——
英文名称
3,5-dimethoxypyrazine-2-carboxylic acid
英文别名
3,5-Dimethoxypyrazine-2-carboxylic acid
3,5-dimethoxypyrazine-2-carboxylic acid化学式
CAS
1286756-62-4
化学式
C7H8N2O4
mdl
——
分子量
184.152
InChiKey
OZKVFTVZLFSJQX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    81.5
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    methyl 3,5-dimethoxypyrazine-2-carboxylate甲醇 、 potassium hydroxide 作用下, 反应 17.0h, 以96%的产率得到3,5-dimethoxypyrazine-2-carboxylic acid
    参考文献:
    名称:
    [EN] PERFLUORINATED CYCLOPROPYL FUSED 1,3-OXAZIN-2-AMINE COMPOUNDS AS BETA-SECRETASE INHIBITORS AND METHODS OF USE
    [FR] COMPOSÉS À BASE DE 1,3-OXAZIN-2-AMINE FUSIONNÉE AVEC DU CYCLOPROPYLE PERFLUORÉ UTILISABLES EN TANT QU'INHIBITEURS DE LA BÊTA-SÉCRÉTASE ET LEURS PROCÉDÉS D'UTILISATION
    摘要:
    本发明提供了一类新的化合物,用于调节β-分泌酶(BACE)活性。这些化合物具有一般的化学式I:{在此插入结构} I,其中变量A4、A5、A6、A8,以及化学式I中的每个Ra、Rb、R1、R2、R3和R7,在本文中分别定义。该发明还提供了包含这些化合物的药物组合物,以及用于治疗与A-beta斑块形成和沉积相关的疾病和/或症状的化合物和组合物的用途,这些疾病和症状是由BACE的生物活性引起的。这种由BACE介导的疾病包括阿尔茨海默病、认知缺陷、认知障碍、精神分裂症和其他中枢神经系统疾病。该发明还提供了化学式II和III的化合物,以及其亚式化合物、中间体和制备本发明化合物的方法。
    公开号:
    WO2014138484A1
点击查看最新优质反应信息

文献信息

  • Iminothiadiazine Dioxide Compounds as BACE Inhibitors, Compositions and Their Use
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20150307465A1
    公开(公告)日:2015-10-29
    In its many embodiments, the present invention provides certain iminothiadiazine dioxide compounds, including compounds Formula (I): and include stereoisomers thereof, and pharmaceutically acceptable salts of said compounds stereoisomers, wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , ring A, ring B, m, n, p, -L 1 -, -L 2 -, and -L 3 - is selected independently and as defined herein. The novel iminothiadiazine dioxide compounds of the invention have surprisingly been found to exhibit properties which are expected to render them advantageous as BACE inhibitors and/or for the treatment and prevention of various pathologies related to β-amyloid (“Aβ”) production. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use in treating pathologies associated with amyloid beta (Aβ) protein, including Alzheimer's disease, are also disclosed.
    本发明提供了多种形式的亚氨基噻二唑二氧化物化合物,包括公式(I)的化合物: 包括它们的立体异构体,以及所述立体异构体的药用可接受盐,其中R1、R2、R3、R4、R5、R9、环A、环B、m、n、p、-L1-、-L2-和-L3-都是独立选择且按本文定义。发明的新型亚氨基噻二唑二氧化物化合物出人意料地被发现具有预期的特性,使其作为BACE抑制剂以及/或用于治疗和预防与β-淀粉样蛋白(“Aβ”)生成相关的各种病理学具有优势。还公开了包含一个或多个此类化合物(单独使用和与一个或多个其他活性成分组合使用)的药物组合物,以及它们的制备方法和用于治疗与淀粉样β(Aβ)蛋白相关的病理学,包括阿尔茨海默病的方法。
  • AMINO-DIHYDROTHIAZINE AND AMINO-DIOXIDO DIHYDROTHIAZINE COMPOUNDS AS BETA-SECRETASE ANTAGONISTS AND METHODS OF USE
    申请人:Amgen Inc.
    公开号:US20140107109A1
    公开(公告)日:2014-04-17
    The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula I: wherein variables A 4 , A 5 , A 6 , A 8 , R 1 , R 2 , R 3 , R 7 and n of Formula I, independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and corresponding uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formula II and sub-formula embodiments thereof, intermediates and processes and methods useful for the preparation of compounds of Formulas I-II.
    本发明提供了一类新的化合物,用于调节β-分泌酶(BACE)活性。这些化合物具有一般的化学式I: 其中化学式I中的变量A4、A5、A6、A8、R1、R2、R3、R7和n在此独立地被定义。该发明还提供了包含这些化合物的药物组合物,以及这些化合物和组合物用于治疗与A-beta斑块形成和沉积相关的疾病和/或症状的对应用途,这些疾病和症状是由BACE的生物活性引起的。这种由BACE介导的疾病包括阿尔茨海默病、认知缺陷、认知障碍、精神分裂症和其他中枢神经系统疾病。该发明还提供了化学式II的化合物及其亚式化合物,中间体和用于制备化学式I-II化合物的有用过程和方法。
  • IMINOTHIADIAZINE DIOXIDE COMPOUNDS AS BACE INHIBITORS, COMPOSITIONS AND THEIR USE
    申请人:Scott Jack D.
    公开号:US20120183563A1
    公开(公告)日:2012-07-19
    In its many embodiments, the present invention provides certain iminothiadiazine dioxide compounds, including compounds Formula (I): (I) and include stereoisomers thereof, and pharmaceutically acceptable salts of said compounds stereoisomers, wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , ring A, ring B, m, n, p, -L 1 -,L 2 -, and L 3 - is selected independently and as defined herein. The novel iminothiadiazine dioxide compounds of the invention have surprisingly been found to exhibit properties which are expected to render them advantageous as BACE inhibitors and/or for the treatment and prevention of various pathologies related to β-amyloid (Aβ) production. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use in treating pathologies associated with amyloid beta (Aβ) protein, including Alzheimers disease, are also disclosed.
    在其多种实施方式中,本发明提供了某些亚硫酰二氮杂环化合物,包括化合物式(I):(I)及其立体异构体和所述化合物立体异构体的药学上可接受的盐,其中R1、R2、R3、R4、R5、R9、环A、环B、m、n、p、-L1-、L2-和L3-各自独立选择并如所定义。本发明的新型亚硫酰二氮杂环化合物出人意料地表现出预期的性质,使它们作为BACE抑制剂和/或用于治疗和预防与β-淀粉样蛋白(Aβ)产生相关的各种病理学具有优势。还公开了包括一种或多种这样的化合物(单独和与一种或多种其他活性剂的组合)的制药组合物,以及用于治疗与淀粉样β(Aβ)蛋白相关的病理学,包括阿尔茨海默病的方法。
  • IMINOTHIADIAZINE DIOXIDE COMPOUNDS AS BACE INHIBITORS, COMPOSITIONS, AND THEIR USE
    申请人:Scott Jack D.
    公开号:US20140296221A1
    公开(公告)日:2014-10-02
    In its many embodiments, the present invention provides certain iminothiadiazine dioxide compounds, including compounds Formula (I): and include stereoisomers thereof, and pharmaceutically acceptable salts of said compounds stereoisomers, wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , ring A, ring B, m, n, p, -L 1 -, -L 2 -, and -L 3 - is selected independently and as defined herein. The novel iminothiadiazine dioxide compounds of the invention have surprisingly been found to exhibit properties which are expected to render them advantageous as BACE inhibitors and/or for the treatment and prevention of various pathologies related to β-amyloid (“Aβ”) production. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and use in treating pathologies associated with amyloid beta (Aβ) protein, including Alzheimer's disease, are also disclosed.
    在其多种实施方式中,本发明提供了某些亚氨基噻二嗪二氧化物化合物,包括化合物公式(I)的化合物:以及其立体异构体和该化合物立体异构体的药学上可接受的盐,其中每个R1、R2、R3、R4、R5、R9、环A、环B、m、n、p、-L1-、-L2-和-L3-独立选择并在此定义。本发明的新型亚氨基噻二嗪二氧化物化合物出乎意料地表现出有利于作为BACE抑制剂和/或用于治疗和预防与β-淀粉样蛋白(“Aβ”)产生相关的各种病理的性质。还公开了包括一个或多个此类化合物(单独和与一个或多个其他活性剂的组合)的制药组合物,以及用于治疗与淀粉样β(Aβ)蛋白相关的病理,包括阿尔茨海默病的制备和使用方法。
  • Perfluorinated cyclopropyl fused 1,3-oxazin-2-amine compounds as beta-secretase inhibitors and methods of use
    申请人:AMGEN INC.
    公开号:US09085576B2
    公开(公告)日:2015-07-21
    The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula I: wherein variables A4, A5, A6, A8, each of Ra, Rb, R1, R2, R3 and R7 of Formula I, independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formulas II and III, and sub-formula embodiments thereof, intermediates and methods for preparing compounds of the invention.
    本发明提供了一种新的化合物类别,用于调节β-分泌酶酶(BACE)活性。该化合物具有一般式I:其中变量A4、A5、A6、A8,以及式I中的每个Ra、Rb、R1、R2、R3和R7,在此独立地定义。该发明还提供了包含该化合物的药物组合物,并且该化合物和组合物的用途包括治疗与A-beta斑块形成和沉积相关的疾病和/或症状,这是由BACE的生物活性引起的。这种BACE介导的疾病包括阿尔茨海默病、认知缺陷、认知障碍、精神分裂症和其他中枢神经系统疾病。该发明还提供了式II和式III的化合物,以及其子式实施例,中间体和制备该发明化合物的方法。
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