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[1,2,4]Triazolo[1,5-a]pyrazine, 2-ethyl-5,8-dimethyl-

中文名称
——
中文别名
——
英文名称
[1,2,4]Triazolo[1,5-a]pyrazine, 2-ethyl-5,8-dimethyl-
英文别名
2-ethyl-5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazine
[1,2,4]Triazolo[1,5-a]pyrazine, 2-ethyl-5,8-dimethyl-化学式
CAS
——
化学式
C9H12N4
mdl
——
分子量
176.22
InChiKey
SMUNBDAOBVJWBR-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):
    1.3
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    43.1
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Imidazole derivatives as PDE10A enzyme inhibitors
    申请人:Kehler Jan
    公开号:US20120129836A1
    公开(公告)日:2012-05-24
    This invention is directed to compounds, which are PDE10A enzyme inhibitors. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. The present invention also provides processes for the preparation of the compounds of formula I. The present invention further provides a method of treating a subject suffering from a neurodegenerative disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention also provides a method of treating a subject suffering from a drug addiction comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention further provides a method of treating a subject suffering from a psychiatric disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I.
    这项发明涉及一类PDE10A酶抑制剂化合物。该发明提供了一种包含该发明化合物的治疗有效量和药用载体的药物组合物。本发明还提供了制备式I化合物的方法。本发明还提供了一种治疗神经退行性疾病的方法,包括向患有神经退行性疾病的受试者施用式I化合物的治疗有效量。本发明还提供了一种治疗药物成瘾的方法,包括向患有药物成瘾的受试者施用式I化合物的治疗有效量。本发明还提供了一种治疗精神障碍的方法,包括向患有精神障碍的受试者施用式I化合物的治疗有效量。
  • NOVEL PHENYLIMIDAZOLE DERIVATIVE AS PDE10A ENZYME INHIBITOR
    申请人:Ritzén Andreas
    公开号:US20120190685A1
    公开(公告)日:2012-07-26
    This invention provides the compound 5,8-Dimethyl-2-[2-(1-methyl-4-phenyl-1H-imidazol-2-yl)-ethyl]-[1,2,4]thazolo[1,5-a]pyrazine and pharmaceutically acceptable acid addition salts thereof.
    这项发明提供了化合物5,8-二甲基-2-[2-(1-甲基-4-苯基-1H-咪唑-2-基)-乙基]-[1,2,4]噻唑并其药学上可接受的酸盐。
  • Heteroaromatic Phenylimidazole derivatives as PDE10A enzyme inhibitors
    申请人:Püschl Ask
    公开号:US20120309714A1
    公开(公告)日:2012-12-06
    This invention is directed to compounds, which are PDE10A enzyme inhibitors. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. The present invention also provides processes for the preparation of the compounds of formula I. The present invention further provides a method of treating a subject suffering from a neurodegenerative disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention also provides a method of treating a subject suffering from a drug addiction comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention further provides a method of treating a subject suffering from a psychiatric disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I.
    本发明涉及一种PDE10A酶抑制剂化合物。该发明提供了一种药物组成物,包括本发明化合物的治疗有效量和药学上可接受的载体。本发明还提供了制备式I化合物的方法。本发明还提供了一种治疗神经退行性疾病的方法,包括向受试者施用式I化合物的治疗有效量。本发明还提供了一种治疗药物成瘾的方法,包括向受试者施用式I化合物的治疗有效量。本发明还提供了一种治疗精神障碍的方法,包括向受试者施用式I化合物的治疗有效量。
  • 2-ARYLIMIDAZOLE DERIVATIVES AS PDE10A ENZYME INHIBITORS
    申请人:Püschl Ask
    公开号:US20120302548A1
    公开(公告)日:2012-11-29
    This invention is directed to compounds, which are PDE10A enzyme inhibitors. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. The present invention also provides processes for the preparation of the compounds of formula I. The present invention further provides a method of treating a subject suffering from a neurodegenerative disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention also provides a method of treating a subject suffering from a drug addiction comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention further provides a method of treating a subject suffering from a psychiatric disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I.
    本发明涉及一种PDE10A酶抑制剂化合物。本发明提供一种药物组合物,该药物组合物包括本发明的化合物的治疗有效量和药学上可接受的载体。本发明还提供了制备式I化合物的方法。本发明还提供了一种治疗神经退行性疾病的方法,包括向患者施用式I化合物的治疗有效量。本发明还提供了一种治疗药物成瘾的方法,包括向患者施用式I化合物的治疗有效量。本发明还提供了一种治疗精神障碍的方法,包括向患者施用式I化合物的治疗有效量。
  • Heteroaromatic aryl triazole derivatives as PDE10A enzyme inhibitors
    申请人:Püschl Ask
    公开号:US20120309764A1
    公开(公告)日:2012-12-06
    This invention is directed to compounds, which are PDE10A enzyme inhibitors. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. The present invention also provides processes for the preparation of the compounds of formula I. The present invention further provides a method of treating a subject suffering from a neurodegenerative disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention also provides a method of treating a subject suffering from a drug addiction comprising administering to the subject a therapeutically effective amount of a compound of formula I. The present invention further provides a method of treating a subject suffering from a psychiatric disorder comprising administering to the subject a therapeutically effective amount of a compound of formula I.
    本发明涉及一种PDE10A酶抑制剂化合物。本发明提供一种药物组合物,包括本发明化合物的治疗有效量和药学上可接受的载体。本发明还提供了制备式I化合物的方法。本发明还提供了一种治疗神经退行性疾病的方法,包括向患者施用式I化合物的治疗有效量。本发明还提供了一种治疗药物成瘾的方法,包括向患者施用式I化合物的治疗有效量。本发明还提供了一种治疗精神障碍的方法,包括向患者施用式I化合物的治疗有效量。
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同类化合物

西他列汀杂质10 [1,2,4]噻唑并[1,5-a]吡嗪-2-胺 N-(1,1-二甲基乙基)-5,6,7,8-四氢-1,2,4-噻唑并[4,3-a]吡嗪-3-羧胺 8-苯基-3-(三氟甲基)-5,6,7,8-四氢-[1,2,4]三唑并[4,3-a]吡嗪盐酸盐 8-肼基-[1,2,4]三唑并[1,5-a]吡嗪 8-甲基-3-(三氟甲基)-5,6,7,8-四氢[1,2,4]三唑并[4,3-a]吡嗪盐酸盐(1:1) 8-甲基-3-(三氟甲基)-5,6,7,8-四氢[1,2,4]三唑并[4,3-a]吡嗪 8-氯[1,2,4]噻唑并[1,5-a]吡嗪 7-Boc-5,6,7,8-四氢-1,2,4-三唑并[4,5-a]吡嗪-3-甲酸乙酯 7-Boc-5,6,7,8-四氢-1,2,4-三唑并[4,3-a]吡嗪 7-Boc-3-溴-5,6,7,8-四氢-1,2,4-三唑并[4,3-a]吡嗪 7-(叔丁氧基羰基)-5,6,7,8-四氢-[1,2,4]噻唑并[4,3-a]吡嗪-3-羧酸 6-溴-[1,2,4]噻唑并[1,5-a]吡嗪-2-胺 6-溴-[1,2,4]三唑并[1,5-a]吡嗪 6-溴-2-(呋喃-2-基)[1,2,4]噻唑并[1,5-a]吡嗪-8-胺 6-氯-2-甲基-[1,2,4]三唑并[1,5-A]吡嗪 6-氨基-[1,2,4]三唑并[1,5-a]吡嗪-8(7H)-酮 6,8-二溴-[1,2,4]噻唑并[1,5-a]吡嗪 6,8-二溴-2-甲基-[1,2,4]三唑并[1,5-A]吡嗪 5-溴-[1,2,4]噻唑并[1,5-a]吡嗪 5,8-二溴-[1,2,4]噻唑并[1,5-a]吡嗪 5,6,7,8-四氢-[1,2,4]三唑并[4,3-A]吡嗪盐酸盐 5,6,7,8-四氢-5-甲基-3-三氟甲基-1,2,4-噻唑并[4,3-a]吡嗪 5,6,7,8-四氢-5,8-二甲基-3-三氟甲基-1,2,4-噻唑并[4,3-a]吡啶 5,6,7,8-四氢-5,5-二甲基-3-(三氟甲基)-1,2,4-噻唑[4,3-A]吡嗪 5,6,7,8-四氢-3-甲氧基-1,2,4-噻唑并[4,3-a]吡嗪 5,6,7,8-四氢-1,2,4-三氮唑并[4,3-A]吡嗪-3-甲醇 5,6,7,8-四氢-1,2,4-三唑并[4,3-a]吡嗪盐酸盐 5,6,7,8-四氢-1,2,4-三唑并[4,3-a]吡嗪-3-甲酸乙酯 5,6,7,8-四氢-1,2,4-三唑并[4,3-A]吡嗪-3-羧酸乙酯盐酸盐 3-甲酰基-5,6-二氢-[1,2,4]三唑并[4,3-A]吡嗪-7(8H)-羧酸叔丁酯 3-甲氧基-5,6-二氢-[1,2,4]噻唑并[4,3-a]吡嗪-7(8h)-羧酸叔丁酯 3-甲基-5,6,7,8-四氢-[1,2,4]三唑并[4,3-A]吡嗪 3-环丙基-5,6,7,8-四氢-[1,2,4]三唑并[4,3-a]吡嗪 3-溴-5,6,7,8-四氢[1,2,4]噻唑并[4,3-a]吡嗪盐酸盐 3-溴-5,6,7,8-四氢-[1,2,4]三唑并[4,3-A]吡嗪盐酸盐 3-异丙基5,6,7,8-四氢[1,2,4]三唑[4,3-A]吡嗪 3-乙基-5,6,7,8-四氢-1,2,4-三唑并[4,3-a]吡嗪 3-三氟甲基-5,6,7,8-四氢-1,2,4-三唑并[4,3-a]吡嗪盐酸盐 3-(三氟甲基)-5,6-二氢-[1,2,4]噻唑[4,3-A]吡嗪-7(8H)-羧酸叔丁酯 3-(三氟甲基)-5,6,7,8-四氢-[1,2,4]三唑并[4,3-a]吡嗪 3-(4-氟苄基)-5,6,7,8-四氢-[1,2,4]三唑并[4,3-a]吡嗪 2-甲基-[1,2,4]噻唑并[1,5-a]吡嗪 2-环丙基-[1,2,4]噻唑并[1,5-a]吡嗪 2-(三氟甲基)-[1,2,4]噻唑并[1,5-A]吡嗪 2,5,8-三甲基[1,2,4]噻唑并[1,5-a]吡嗪 (2Z)-4-氧代-4-[3-(三氟甲基)-5,6-二氢-[1,2,4]三唑并[4,3-a]吡嗪-7-(8H)-基]-1-(2,4,5-三氟苯基)丁-2-酮 (2Z)-4-氧代-4-[3-(三氟甲基)-5,6-二氢-[1,2,4]三唑并[4,3-a]吡嗪-7(8H)-基]-1-(2,4,5-三氟苯基)丁-2-烯-2-胺 (2Z)-1-[5,6-二氢-3-(三氟甲基)-1,2,4-三唑并[4,3-a]吡嗪-7(8H)-基]-3-[[(1R)-1-苯乙基]氨基]-4-(2,4,5-三氟苯基)-2-丁烯-1-酮 (1,2,4)噻唑(1,5-a)吡嗪