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2,4-di-tert-butyl-6-{4-[3-(4,5-dimethyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-pyrimidine benzenesulfonic acid salt

中文名称
——
中文别名
——
英文名称
2,4-di-tert-butyl-6-{4-[3-(4,5-dimethyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-pyrimidine benzenesulfonic acid salt
英文别名
2,4-di-tert-butyl-6-{4-[3-(4,5-dimethyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-pyrimidine benzenesulfonate;benzenesulfonic acid;2,4-ditert-butyl-6-[4-[3-[(4,5-dimethyl-1,2,4-triazol-3-yl)sulfanyl]propyl]piperazin-1-yl]pyrimidine
2,4-di-tert-butyl-6-{4-[3-(4,5-dimethyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-pyrimidine benzenesulfonic acid salt化学式
CAS
——
化学式
C6H6O3S*C23H39N7S
mdl
——
分子量
603.853
InChiKey
QIUASXMUGBPOFJ-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):
    4.75
  • 重原子数:
    41
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    151
  • 氢给体数:
    1
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    2-tert-Butyl-4-{4-[3-(4-methyl-5-methyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-6-tert-butyl-pyrimidine苯磺酸 作用下, 以 正庚烷乙酸乙酯 为溶剂, 以90.9%的产率得到2,4-di-tert-butyl-6-{4-[3-(4,5-dimethyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-pyrimidine benzenesulfonic acid salt
    参考文献:
    名称:
    Triazole compounds suitable for treating disorders that respond to modulation of the dopamine D3 receptor
    摘要:
    该发明涉及一般式I的三唑化合物,其中R1为氢或甲基,R2为C3-C4烷基或C1-C2氟烷基,以及这些化合物的生理耐受酸盐。该发明还涉及一种包含至少一种一般式I的三唑化合物和/或至少一种其生理耐受酸盐的药物组合物,以及一种用于治疗对多巴胺D3受体拮抗剂或多巴胺D3激动剂有益反应的疾病的方法,该方法包括向需要的受试者施用至少一种一般式I的三唑化合物或其生理耐受酸盐的有效量。
    公开号:
    US20040259882A1
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文献信息

  • [EN] TRIAZOLE COMPOUNDS SUITABLE FOR TREATING DISORDERS THAT RESPOND TO MODULATION OF THE DOPAMINE D3 RECEPTOR<br/>[FR] COMPOSES TRIAZOLE UTILISES DANS LE TRAITEMENT DE TROUBLES REAGISSANT A LA MODULATION DU RECEPTEUR DE DOPAMINE D3
    申请人:ABBOTT GMBH & CO KG
    公开号:WO2004108706A1
    公开(公告)日:2004-12-16
    The invention relates to triazole compounds of the general formula I wherein R1 is hydrogen or methyl, and R2 is C3-C4alkyl or C1-C2fluoroalkyl, as well as the physiologically tolerated acid addition salts of these compounds. The invention also relates to a pharmaceutical composition that comprises at least one triazole compound of the formula (I) and/or at least one physiologically tolerated acid addition salt thereof, and further to a method for treating disorders that respond beneficially to dopamine D3 receptor antagonists or dopamine D3agonists, said method comprising administering an effective amount of at least one triazole compound or physiologically tolerated acid addition salt of the formula (I) to a subject in need thereof.
    本发明涉及通式I的三唑类化合物,其中R1为氢或甲基,R2为C3-C4烷基或C1-C2氟烷基,以及这些化合物的生理可耐受的酸盐。本发明还涉及一种制药组合物,该组合物包括至少一种通式(I)的三唑化合物和/或至少一种生理可耐受的酸盐,以及一种用于治疗对多巴胺D3受体拮抗剂或多巴胺D3激动剂有益反应的障碍的方法,该方法包括向需要的受体中注射至少一种通式(I)的三唑化合物或生理可耐受的酸盐的有效量。
  • Triazole compouds suitable for treating disorders that respond to modulation of the dopamine D3 receptor
    申请人:Abbott GmbH & Co. KG
    公开号:EP1484330B1
    公开(公告)日:2005-10-26
  • US6919342B2
    申请人:——
    公开号:US6919342B2
    公开(公告)日:2005-07-19
  • Triazole compounds suitable for treating disorders that respond to modulation of the dopamine D3 receptor
    申请人:——
    公开号:US20040259882A1
    公开(公告)日:2004-12-23
    The invention relates to triazole compounds of the general formula I 1 wherein R 1 is hydrogen or methyl, and R 2 is C 3 -C 4 alkyl or C 1 -C 2 fluoroalkyl, as well as the physiologically tolerated acid addition salts of these compounds. The invention also relates to a pharmaceutical composition that comprises at least one triazole compound of the formula I and/or at least one physiologically tolerated acid addition salt thereof, and further to a method for treating disorders that respond beneficially to dopamine D 3 receptor antagonists or dopamine D 3 agonists, said method comprising administering an effective amount of at least one triazole compound or physiologically tolerated acid addition salt of the formula I to a subject in need thereof.
    该发明涉及一般式I的三唑化合物,其中R1为氢或甲基,R2为C3-C4烷基或C1-C2氟烷基,以及这些化合物的生理耐受酸盐。该发明还涉及一种包含至少一种一般式I的三唑化合物和/或至少一种其生理耐受酸盐的药物组合物,以及一种用于治疗对多巴胺D3受体拮抗剂或多巴胺D3激动剂有益反应的疾病的方法,该方法包括向需要的受试者施用至少一种一般式I的三唑化合物或其生理耐受酸盐的有效量。
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