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2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole | 111371-26-7

中文名称
——
中文别名
——
英文名称
2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole
英文别名
2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole
2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole化学式
CAS
111371-26-7
化学式
C12H11N3O2S2
mdl
——
分子量
293.37
InChiKey
YHQTXIPXCODMTK-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):
    1.2
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    115
  • 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:
    参考文献:
    名称:
    2-[((2-吡啶基甲基)亚磺酰基] -1H-噻吩并[3,4-d]咪唑。一类新型的胃H + / K(+)-ATPase抑制剂。
    摘要:
    合成2-[((2-吡啶基甲基)亚磺酰基]噻吩并咪唑类化合物,并研究其作为胃H + / K(+)-ATPase的潜在抑制剂。已发现两种可能的噻吩并咪唑系列的[3,4-d]异构体在体外和体内都是有效的胃酸分泌抑制剂。结构活性关系表明,特别是在吡啶部分的4位具有额外的电子要求特性的亲脂性烷氧基,苄氧基和苯氧基取代基与未取代的噻吩并[3,4-d]咪唑结合会导致具有高活性的化合物。良好的化学稳定性。噻吩并[3,4-d]咪唑部分的各种取代方式导致较低的生物活性。选择了七氟丁氧基衍生物萨维拉唑(HOE 731,5d)进行进一步开发,目前正在临床评估中。
    DOI:
    10.1021/jm00081a004
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文献信息

  • Substituierte Thienoimidazol-Derivate, Verfahren zu ihrer Herstellung, sie enthaltende pharmazeutische Zubereitungen und ihre Verwendung als Magensäuresekretionshemmer
    申请人:HOECHST AKTIENGESELLSCHAFT
    公开号:EP0234485B1
    公开(公告)日:1992-04-01
  • LANG, HANS-JOCHEN;RIPPEL, ROBERT;HERLING, ANDREAS
    作者:LANG, HANS-JOCHEN、RIPPEL, ROBERT、HERLING, ANDREAS
    DOI:——
    日期:——
  • Homogeneous paste and gel formulations
    申请人:Nached Hassan
    公开号:US20080027011A1
    公开(公告)日:2008-01-31
    This invention provides for a pharmaceutical or veterinary paste or gel formulation which may comprise an effective amount of a therapeutic agent; optionally an absorbent or a viscosity modifier; optionally a hydrophilic carrier, a colorant, stabilizer, surfactant, or preservative and optionally an antioxidant, solvent, flavoring, buffering system or thickener and methods of preparing these formulations. This invention also provides for, inter alia, oral homogeneous veterinary pastes or gels for the treating, controlling and preventing of endo- and ectoparasite infections in warm-blooded animals, such as birds, horses and household pets.
  • Oral Pharmaceutical Dosage Forms Comprising a Proton Pump Inhibitor and a NSAID
    申请人:Depui Helene
    公开号:US20090297594A1
    公开(公告)日:2009-12-03
    An oral pharmaceutical dosage form comprising an acid susceptible proton pump inhibitor and one or more NSAIDs in a fixed formulation, wherein the proton pump inhibitor is protected by an enteric coating layer. The fixed formulation is in the form of an enteric coating layered tablet, a capsule or a multiple unit tableted dosage form. The multiple unit dosage forms are most preferred. The new fixed formulation is especially useful in the treatment of gastrointestinal side-effects associated with NSAID treatment.
  • US4845118A
    申请人:——
    公开号:US4845118A
    公开(公告)日:1989-07-04
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同类化合物

沙维拉唑 4H-吡咯并[1,2-a]噻吩并[3,2-D]咪唑 3H-噻吩并[2,3-d]咪唑-5-羧酸 3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮 2-(氯甲基)-1H-噻吩并[3,4-d]咪唑 1H-噻吩并[3,2-D]咪唑-2(3H)-酮 1H-噻吩并[2,3-d]咪唑,1-乙烯基-(9CI) 1H-噻吩并(3,4-d)咪唑,2-(((5-甲基-2-吡啶基)甲基)亚硫酰基)- 1-甲基-1H-噻吩并[2,3-D]咪唑基-2(3H)-酮 1-乙烯基-1H-噻吩并[2,3-d]咪唑-5-羧酸 1,3-二氢噻吩并[3,4-d]咪唑-2-硫酮 tert-butyl 4-[4-(2,3-dihydro-2-oxo-1-tert-butoxycarbonyl-1H-thieno[3,4-d]imidazol-4-yl)phenyl]-2,3-dihydro-2-oxo-1H-thieno[3,4-d]imidazole-1-carboxylate 2-(3-Bromo-4-methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-[3-Methoxy-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethylsulfanyl]-1H-thieno[3,4-d]imidazole 2-(2-diethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole 2-(5-Bromo-4-methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-(5-Chloro-4-methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-(2-dimethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole 6-amino-1-vinylthieno[2,3-d]imidazole-5-carboxamide 1-Vinyl-1H-thieno[2,3-d]imidazole-5-carboxylic acid ethyl ester 2-(3-Chloro-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(5-Methoxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole (2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-thieno[2,3-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate 1-methyl-2-methoxymethyl-thieno[2.3-d]imidazol-5-yl-carboxylic acid 2-(3-Fluoro-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(4-Benzyloxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[2,3-d]imidazole 4-(4-methoxyphenyl)-2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-(4-methoxy-2-picolylmercapto)-1H-thieno[3,4-d]imidazole methyl 2-[(4-methoxypyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole-4-carboxylate 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-4-phenyl-1H-thieno[3,4-d]imidazole dimethyl 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[2,3-d]imidazole-5,6-dicarboxylate 2-[(4-methoxypyridin-2-yl)methylsulfanyl]-1H-thieno[2,3-d]imidazole methyl 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole-4-carboxylate 1-Ethoxycarbonyl-2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole 1-ethoxycarbonyl-2-(4-methoxy-2-picolylmercapto)-1H-thieno[3,4-d]imidazole ethyl 2-methylthieno[2,3-d]imidazol-5-carboxylate 2-[(5-chloropyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(4-Thiazolyl)methylthio]thieno[3,4-d]imidazole 2-[[3-Methoxy-4-(2,2,3,3,4,4,4-heptafluorobutoxy)-2-pyridinyl]methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(3-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(3,4-dimethoxypyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole 2-[(3,4-dimethoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-4-(4-methoxyphenyl)-1H-thieno[3,4-d]imidazole 2-(4-methoxy-3,5-dimethyl-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-4-phenyl-1H-thieno[3,4-d]imidazole 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole (3S,3'S,5S,5'S)-tert-butyl 5,5'-(5,5'-(buta-1,3-diyne-1,4-diyl)bis(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-thieno[2,3-d]imidazole-5,2-diyl))bis(3-methylpyrrolidine-1-carboxylate) (2S,4S)-tert-butyl 2-(5-ethynyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-thieno[2,3-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate