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4-chloro-1-(difluoromethyl)-N-methoxy-N-methyl-1H-pyrazole-3-carboxamide | 1357098-10-2

中文名称
——
中文别名
——
英文名称
4-chloro-1-(difluoromethyl)-N-methoxy-N-methyl-1H-pyrazole-3-carboxamide
英文别名
4-chloro-1-difluoromethyl-1H-pyrazole-3-carboxylic acid methoxy-methyl-amide;4-chloro-1-difluoromethyl-1H-pyrazole-3-carboxylic acid N-methoxy-N-methyl-amide;4-chloro-1-(difluoromethyl)-N-methoxy-N-methylpyrazole-3-carboxamide
4-chloro-1-(difluoromethyl)-N-methoxy-N-methyl-1H-pyrazole-3-carboxamide化学式
CAS
1357098-10-2
化学式
C7H8ClF2N3O2
mdl
——
分子量
239.609
InChiKey
XUYOHNVLFNAEDF-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

物化性质

  • 沸点:
    351.1±42.0 °C(Predicted)
  • 密度:
    1.49±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    47.4
  • 氢给体数:
    0
  • 氢受体数:
    5

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • 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。
  • 1,4-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS
    申请人:Gabellieri Emanuele
    公开号:US20120238548A1
    公开(公告)日:2012-09-20
    The present invention relates to 1,4-Oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
    本发明涉及具有BACE1和/或BACE2抑制活性的式I的1,4-噁唑啉,其制备方法,含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗例如阿尔茨海默病和2型糖尿病方面是有用的。
  • [EN] 1,4-OXAZEPINES AS BACE1 AND/OR BACE2 INHIBITORS<br/>[FR] 1,4-OXAZÉPINES UTILISABLES EN TANT QU'INHIBITEURS DE BACE1 ET/OU BACE2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2012126791A1
    公开(公告)日:2012-09-27
    The present invention relates to 1,4-Oxazepines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
    本发明涉及具有BACE1和/或BACE2抑制活性的式I的1,4-噁唑啉,它们的制备,含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗例如阿尔茨海默病和2型糖尿病方面是有用的。
  • [EN] 1,3-OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS<br/>[FR] 1,3-OXAZINES EN TANT QU'INHIBITEURS DE BACE1 ET/OU DE BACE2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2012156284A1
    公开(公告)日:2012-11-22
    The present invention provides compounds of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
    本发明提供具有BACE1和/或BACE2抑制活性的式I化合物,它们的制备方法,含有它们的制药组合物以及它们作为治疗活性物质的用途。本发明的活性化合物可用于治疗和/或预防例如阿尔茨海默病和2型糖尿病等疾病。
  • [EN] 1,4 OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS<br/>[FR] 1,4 OXAZINES UTILISÉS COMME INHIBITEURS DE BACE1 ET/OU BACE2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2012098064A1
    公开(公告)日:2012-07-26
    The present invention relates to 1,4 Oxazines of formula (I): having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
    本发明涉及具有BACE1和/或BACE2抑制活性的式(I)的1,4噁嗪,它们的制备,含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗例如阿尔茨海默病和2型糖尿病方面是有用的。
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