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2-ethyl-4-thiazolemethanamine | 933707-20-1

中文名称
——
中文别名
——
英文名称
2-ethyl-4-thiazolemethanamine
英文别名
(2-Ethyl-1,3-thiazol-4-yl)methanamine
2-ethyl-4-thiazolemethanamine化学式
CAS
933707-20-1
化学式
C6H10N2S
mdl
MFCD09693918
分子量
142.225
InChiKey
HZZPGOJICYGVTC-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:
    235.7±15.0 °C(Predicted)
  • 密度:
    1.138±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    67.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    5-amino-2-cyclopropyl-4,6-dichloropyrimidine2-ethyl-4-thiazolemethanamineN,N-二异丙基乙胺 作用下, 以 N-甲基吡咯烷酮 为溶剂, 反应 18.0h, 生成 6-chloro-2-cyclopropyl-4-N-[(2-ethyl-1,3-thiazol-4-yl)methyl]pyrimidine-4,5-diamine
    参考文献:
    名称:
    Discovery of triazolopyrimidine-based PDE8B inhibitors: Exceptionally ligand-efficient and lipophilic ligand-efficient compounds for the treatment of diabetes
    摘要:
    PDE8B is a cAMP-specific isoform of the broader class of phosphodiesterases (PDEs). As no selective PDE8B inhibitors had been reported, a high throughput screen was run with the goal of identifying selective tools for exploring the potential therapeutic utility of PDE8B inhibition. Of the numerous hits, one was particularly attractive since it was amenable to rapid deconstruction leading to inhibitors with very high ligand efficiency (LE) and lipophilic ligand efficiency (LLE). These triazolopyrimidines were optimized for potency, selectivity and ADME properties ultimately leading to compound 42. This compound was highly potent and selective with good bioavailability and advanced into pre-clinical development. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.06.079
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文献信息

  • [EN] PPAR AGONISTS<br/>[FR] ANTAGONISTES DE PPAR
    申请人:SALK INST FOR BIOLOGICAL STUDI
    公开号:WO2014165827A1
    公开(公告)日:2014-10-09
    Provided herein are compounds and compositions useful in increasing PPARδ activity. The compounds and compositions provided herein are useful for the treatment of PPARδ related diseases (e.g., muscular diseases, vascular disease, demyelinating disease, and metabolic diseases).
    本文提供的化合物和组合物可用于增加PPARδ活性。本文提供的化合物和组合物可用于治疗与PPARδ相关的疾病(例如肌肉疾病、血管疾病、脱髓鞘疾病和代谢性疾病)。
  • HETEROARYLMETHYL AMIDES
    申请人:Hebeisen Paul
    公开号:US20120065212A1
    公开(公告)日:2012-03-15
    The present invention relates to compounds of the formula wherein A 1 , A 2 , A 3 and R 1 to R 8 are defined in the description, and to pharmaceutically acceptable salts thereof, their manufacture, pharmaceutical compositions containing them and their use as medicaments for the treatment and/or prophylaxis of diseases which can be treated with HDL-cholesterol raising agents, such as particularly dyslipidemia, atherosclerosis and cardiovascular diseases.
    本发明涉及以下公式的化合物,其中A1、A2、A3和R1至R8在描述中有定义,并且其药用盐,其制备,含有它们的药物组合物以及它们作为药物用于治疗和/或预防可用高密度脂蛋白胆固醇升高剂治疗的疾病,例如特别是血脂异常、动脉粥样硬化和心血管疾病。
  • [EN] HETEROARYLMETHYL AMIDES<br/>[FR] HÉTÉROARYLMÉTHYL-AMIDES
    申请人:HOFFMANN LA ROCHE
    公开号:WO2012032018A1
    公开(公告)日:2012-03-15
    The present invention relates to compounds of the formula I wherein A1, A2, A3 and R1 to R8 are defined in the description, and to pharmaceutically acceptable salts thereof, their manufacture, pharmaceutical compositions containing them and their use as medicaments for the treatment and/or prophylaxis of diseases which can be treated with HDL-cholesterol raising agents, such as particularly dyslipidemia, atherosclerosis and cardiovascular diseases.
    本发明涉及公式I中的化合物,其中A1、A2、A3和R1至R8在描述中有定义,以及其药用盐,其制备方法,含有它们的药物组合物以及它们作为药物用于治疗和/或预防可以用HDL-胆固醇升高剂治疗的疾病,如特别是脂质代谢异常、动脉粥样硬化和心血管疾病。
  • Heteroarylmethyl amides
    申请人:Hoffman-La Roche Inc.
    公开号:US09090599B2
    公开(公告)日:2015-07-28
    The present invention relates to compounds of the formula wherein A1, A2, A3 and R1 to R8 are defined in the description, and to pharmaceutically acceptable salts thereof, their manufacture, pharmaceutical compositions containing them and their use as medicaments for the treatment and/or prophylaxis of diseases which can be treated with HDL-cholesterol raising agents, such as particularly dyslipidemia, atherosclerosis and cardiovascular diseases.
    本发明涉及以下式子的化合物:其中A1,A2,A3和R1至R8在描述中有定义,并且其药学上可接受的盐、其制造、包含它们的制药组合物以及它们作为治疗和/或预防可用高密度脂蛋白胆固醇升高剂治疗的疾病的药物的使用,例如特别是脂质代谢异常、动脉硬化和心血管疾病。
  • US8729105B2
    申请人:——
    公开号:US8729105B2
    公开(公告)日:2014-05-20
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