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2-(4-乙酰基吡嗪-1-基)吡啶-5-硼酸频那醇酯 | 1073372-01-6

中文名称
2-(4-乙酰基吡嗪-1-基)吡啶-5-硼酸频那醇酯
中文别名
2-(4-乙酰基哌嗪-1-基)吡啶-5-硼酸频哪醇酯
英文名称
1-(4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazin-1-yl)ethan-1-one
英文别名
1-(4-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazin-1-yl)ethanone;1-[4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]piperazin-1-yl]ethanone
2-(4-乙酰基吡嗪-1-基)吡啶-5-硼酸频那醇酯化学式
CAS
1073372-01-6
化学式
C17H26BN3O3
mdl
——
分子量
331.223
InChiKey
RNFCDPMIZSSWDQ-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:
    518.3±50.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.05
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    54.9
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 危险品标志:
    T
  • 危险类别码:
    R25
  • 危险品运输编号:
    UN 2811 6.1 / PGIII
  • WGK Germany:
    3
  • 海关编码:
    2934999090
  • 包装等级:
    III
  • 危险类别:
    6.1
  • 危险性防范说明:
    P301+P310
  • 危险性描述:
    H301

反应信息

  • 作为反应物:
    描述:
    2-(4-乙酰基吡嗪-1-基)吡啶-5-硼酸频那醇酯 、 ethyl 1-[1-{5-chloro-2-[(trifluoromethanesulfonyl)oxy]phenyl}piperidin-3-yl]-5-(difluoromethyl)-1H-pyrazole-4-carboxylate 在 四(三苯基膦)钯 、 sodium carbonate 、 、 lithium hydroxide 、 盐酸 作用下, 以 乙醇甲苯四氢呋喃1,4-二氧六环 为溶剂, 生成 1-(1-{2-[6-(4-acetylpiperazin-1-yl)pyridin-3-yl]-5-chlorophenyl}piperidin-3-yl)-5-(difluoromethyl)-1H-pyrazole-4-carboxylic acid hydrochloride
    参考文献:
    名称:
    [EN] SUBSTITUTED PYRAZOLO PIPERIDINE CARBOXYLIC ACIDS
    [FR] ACIDES PYRAZOLO PIPÉRIDINE CARBOXYLIQUES SUBSTITUÉS
    摘要:
    本发明涉及取代的吡唑啉哌啶羧酸及其盐的制备方法,以及它们用于制备治疗和/或预防疾病的药物,特别是心血管和心脏疾病,优选为收缩功能减弱和保留的心衰(HFrEF,HFmrEF和HFpEF),高血压(HTN),周围动脉疾病(PAD,PAOD),心肾和肾脏疾病,优选为慢性和糖尿病肾病(CKD和DKD),心肺和肺部疾病,优选为肺动脉高压(PH),以及其他疾病,优选为神经退行性疾病和不同形式的痴呆症,纤维性疾病,系统性硬化症(SSc),镰状细胞病(SCD),创面愈合障碍,如糖尿病足溃疡(DFU)。
    公开号:
    WO2022122913A1
  • 作为产物:
    描述:
    4-BOC-1-(5-溴-2-吡啶基)哌嗪盐酸 、 palladium [2'-(amino-κN)[1,1'-biphenyl]-2-yl-κC][[5-(diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]diphenylphosphine-κP](methanesulfonato-κO) 、 potassium acetate三乙胺 作用下, 以 1,4-二氧六环4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 为溶剂, 反应 29.0h, 生成 2-(4-乙酰基吡嗪-1-基)吡啶-5-硼酸频那醇酯
    参考文献:
    名称:
    [EN] FUSED HETEROCYCLIC COMPOUNDS AS PI3KALPHA INHIBITORS
    [FR] COMPOSÉS HÉTÉROCYCLIQUES CONDENSÉS UTILISÉS EN TANT QU'INHIBITEURS DE PI3KALPHA
    摘要:
    The present disclosure describes antagonists of the enzyme. The present disclosure provides compounds having a structure set forth in Formula (VI), (VII), (VII-1) or (VIII), the stereoisomer or pharmaceutically acceptable salts, solvates and prodrugs thereof. Further provided are uses of the compounds of Formula (VI), (VII), (VII-1) or (VIII) in treating cancers.
    公开号:
    WO2023104111A1
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文献信息

  • BICYCLIC HETEROCYCLES AS FGFR INHIBITORS
    申请人:Incyte Corporation
    公开号:US20210106588A1
    公开(公告)日:2021-04-15
    The present invention relates to bicyclic heterocycles, and pharmaceutical compositions of the same, that are inhibitors of the FGFR enzyme and are useful in the treatment of FGFR-associated diseases such as cancer.
    这项发明涉及双环杂环化合物及其药物组合物,这些化合物是FGFR酶的抑制剂,可用于治疗与FGFR相关的疾病,如癌症。
  • [EN] SUBSTITUTED PYRAZOLO PIPERIDINE CARBOXYLIC ACIDS<br/>[FR] ACIDES PYRAZOLO PIPÉRIDINE CARBOXYLIQUES SUBSTITUÉS
    申请人:BAYER AG
    公开号:WO2022122913A1
    公开(公告)日:2022-06-16
    The invention relates to substituted pyrazolo piperidine carboxylic acids, their salts and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular and cardiac diseases, preferably heart failure with reduced and preserved ejection fraction (HFrEF, HFmrEF and HFpEF), hypertension (HTN), peripheral arterial diseases (PAD, PAOD), cardio-renal and kidney diseases, preferably chronic and diabetic kidney disease (CKD and DKD), cardiopulmonary and lung diseases, preferable pulmonary hypertension (PH), and other diseases, preferably neurodegenerative diseases and different forms of dementias, fibrotic diseases, systemic sclerosis (SSc), sickle cell disease (SCD), wound healing disorders such as diabetic foot ulcer (DFU).
    本发明涉及取代的吡唑啉哌啶羧酸及其盐的制备方法,以及它们用于制备治疗和/或预防疾病的药物,特别是心血管和心脏疾病,优选为收缩功能减弱和保留的心衰(HFrEF,HFmrEF和HFpEF),高血压(HTN),周围动脉疾病(PAD,PAOD),心肾和肾脏疾病,优选为慢性和糖尿病肾病(CKD和DKD),心肺和肺部疾病,优选为肺动脉高压(PH),以及其他疾病,优选为神经退行性疾病和不同形式的痴呆症,纤维性疾病,系统性硬化症(SSc),镰状细胞病(SCD),创面愈合障碍,如糖尿病足溃疡(DFU)。
  • [EN] FUSED HETEROCYCLIC COMPOUNDS AS PI3KALPHA INHIBITORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES CONDENSÉS UTILISÉS EN TANT QU'INHIBITEURS DE PI3KALPHA
    申请人:[en]NANJING ZENSHINE PHARMACEUTICALS CO., LTD.
    公开号:WO2023104111A1
    公开(公告)日:2023-06-15
    The present disclosure describes antagonists of the enzyme. The present disclosure provides compounds having a structure set forth in Formula (VI), (VII), (VII-1) or (VIII), the stereoisomer or pharmaceutically acceptable salts, solvates and prodrugs thereof. Further provided are uses of the compounds of Formula (VI), (VII), (VII-1) or (VIII) in treating cancers.
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