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5-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)-1H-吲唑-3-胺 | 953411-16-0

中文名称
5-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)-1H-吲唑-3-胺
中文别名
3-氨基-1H-吲唑-5-硼酸频哪醇酯;5-(4,4,5,5-四甲基-1,3,2-二噁硼烷-2-基)-1H-吲唑-3-胺
英文名称
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine
英文别名
3-amino-1H-indazole-5-boronic acid pinacol ester
5-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)-1H-吲唑-3-胺化学式
CAS
953411-16-0
化学式
C13H18BN3O2
mdl
——
分子量
259.116
InChiKey
IVUMUNXPWHOTHY-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:
    469.9±25.0 °C(Predicted)
  • 密度:
    1.20±0.1 g/cm3 (20 ºC 760 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    1.44
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    73.2
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2934999090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335

反应信息

  • 作为反应物:
    描述:
    methyl 8-chloro-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate 、 5-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)-1H-吲唑-3-胺 在 methyl 8-(3-amino-1H-indazol-5-yl)-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate 、 silica 、 二氯甲烷甲醇 作用下, 以afforded the title compound as a yellow solid (32 mg, 42%)的产率得到methyl 8-(3-amino-1H-indazol-5-yl)-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate
    参考文献:
    名称:
    ANTIMICROBIAL 4-OXOQUINOLIZINES
    摘要:
    该发明提供了新型的4-氧喹啉并化合物及其用途,适用于一系列广谱抗生素,不与现有或新出现的抗生素类别产生交叉耐药性。此外,新型的4-氧喹啉并化合物对CDC A和B类病原体也有用。该发明还提供了包含某些4-氧喹啉并化合物与亚抑制浓度的多粘菌素B的药物组合,用于对抗对喹诺酮、碳青霉烯和其他抗微生物药物产生耐药性的临床分离株。
    公开号:
    US20130252882A1
  • 作为产物:
    描述:
    联硼酸频那醇酯 在 (1,5-cyclooctadiene)(methoxy)iridium(I) dimer 、 一水合肼4,4'-二叔丁基-2,2'-二吡啶 作用下, 以 乙醇甲基叔丁基醚 为溶剂, 反应 49.0h, 生成 5-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)-1H-吲唑-3-胺
    参考文献:
    名称:
    10.3390/molecules29153515
    摘要:
    DOI:
    10.3390/molecules29153515
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文献信息

  • [EN] KINASE INHIBITOR COMPOUNDS AND COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSÉS INHIBITEURS DE KINASE, COMPOSITIONS ET MÉTHODES D'UTILISATION
    申请人:ICAHN SCHOOL MED MOUNT SINAI
    公开号:WO2021263129A1
    公开(公告)日:2021-12-30
    Disclosed herein are kinase inhibitor compounds having the structure (I) or a stereoisomer, pharmaceutically acceptable salt, oxide, or solvate thereof, where R1, R2, X, L, Q, and Y are as defined herein. Also disclosed are compositions containing the kinase inhibitor compounds, methods of inhibiting activity of a kinase in a cell, methods of increasing cell proliferation in a population of pancreatic beta cells, methods of treating a subject for a condition associated with insufficient insulin secretion, and methods of treating a subject for a neurological disorder.
    本文披露了具有结构(I)或其立体异构体、药学上可接受的盐、氧化物或溶剂的激酶抑制剂化合物,其中R1、R2、X、L、Q和Y如本文所定义。还披露了含有激酶抑制剂化合物的组合物,抑制细胞中激酶活性的方法,增加胰岛β细胞群体中细胞增殖的方法,治疗因胰岛素分泌不足引起的疾病的方法,以及治疗神经系统疾病的方法。
  • ANTIMICROBIAL 4-OXOQUINOLIZINES
    申请人:Heim Jutta
    公开号:US20130252882A1
    公开(公告)日:2013-09-26
    This invention provides novel 4-oxoquinolizine compounds and their uses for a series of broad-spectrum antibiotics having no cross-resistance to existing or emerging classes of antibiotics. In addition the novel 4-oxoquinolizine compounds are useful against CDC Category A and B pathogens The invention also provides pharmaceutical compositions comprising certain 4-oxoquinolizines in combination with subinhibitory concentrations of polymyxin B against clinical isolates which are resistant to quinolones, carbapenems and other antimicrobial agents.
    该发明提供了新型的4-氧喹啉并化合物及其用途,适用于一系列广谱抗生素,不与现有或新出现的抗生素类别产生交叉耐药性。此外,新型的4-氧喹啉并化合物对CDC A和B类病原体也有用。该发明还提供了包含某些4-氧喹啉并化合物与亚抑制浓度的多粘菌素B的药物组合,用于对抗对喹诺酮、碳青霉烯和其他抗微生物药物产生耐药性的临床分离株。
  • THERAPEUTIC COMPOUNDS
    申请人:Gilead Sciences, Inc.
    公开号:US20160108030A1
    公开(公告)日:2016-04-21
    Compounds of formula (I) or salts thereof are disclosed. Also disclosed are pharmaceutical compositions comprising a compound of formula I, processes for preparing compounds of formula I, intermediates useful for preparing compounds of formula I and therapeutic methods for treating a Retroviridae viral infection including an infection caused by the HIV virus.
    本发明揭示了化学式(I)的化合物或其盐。还揭示了包括化合物I的制药组合物、制备化合物I的方法、制备化合物I有用的中间体以及治疗逆转录病毒感染的治疗方法,包括由HIV病毒引起的感染。
  • Nitrogen-Containing Heterocyclic Compound, Pharmaceutical Compositions thereof and Use thereof
    申请人:280 Bio, Inc.
    公开号:US20240158408A1
    公开(公告)日:2024-05-16
    Disclosed is a nitrogen-containing heterocyclic compound, pharmaceutical compositions thereof and use thereof. The present disclosure provides a nitrogen-containing heterocyclic compound represented by formula I, a pharmaceutically acceptable salt thereof, a solvate thereof, a solvate of pharmaceutically acceptable salt thereof, a crystal thereof, a stereoisomer thereof, a tautomer thereof or an isotopically labeled compound thereof. The nitrogen-containing heterocyclic compound represented by formula I is expected to treat and/or prevent various PI3K-meditated diseases.
  • WO2023/23532
    申请人:——
    公开号:——
    公开(公告)日:——
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