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B-[6-(3-吡啶氧基)-3-吡啶]-硼酸 | 918138-38-2

中文名称
B-[6-(3-吡啶氧基)-3-吡啶]-硼酸
中文别名
——
英文名称
6-(pyridin-3-yloxy)pyridin-3-yl boronic acid
英文别名
6-(Pyridin-3-yloxy)pyridine-3-boronic acid;(6-pyridin-3-yloxypyridin-3-yl)boronic acid
B-[6-(3-吡啶氧基)-3-吡啶]-硼酸化学式
CAS
918138-38-2
化学式
C10H9BN2O3
mdl
——
分子量
216.004
InChiKey
OKBZLPTXOVQGGP-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):
    -0.05
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    75.5
  • 氢给体数:
    2
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    B-[6-(3-吡啶氧基)-3-吡啶]-硼酸邻溴苯甲醛四(三苯基膦)钯 sodium carbonate 作用下, 以 1,4-二氧六环 为溶剂, 反应 15.0h, 以31%的产率得到2-[6-(pyridin-3-yloxy)pyridin-3-yl]benzaldehyde
    参考文献:
    名称:
    Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions
    摘要:
    This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen-metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupling reactions of these novel boronic acids with selected aryl halides is described. This strategy produces novel pyridylethers of interest in cholinergic medicinal chemistry. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.09.036
  • 作为产物:
    描述:
    3-bromo-6-(pyridin-3-yloxy)pyridine正丁基锂硼酸三异丙酯 作用下, 以 乙醚 为溶剂, 反应 1.5h, 以8%的产率得到B-[6-(3-吡啶氧基)-3-吡啶]-硼酸
    参考文献:
    名称:
    Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions
    摘要:
    This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen-metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupling reactions of these novel boronic acids with selected aryl halides is described. This strategy produces novel pyridylethers of interest in cholinergic medicinal chemistry. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.09.036
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文献信息

  • SUBSTITUTED PHENYLALANINE DERIVATIVES
    申请人:BAYER PHARMA AKTIENGESELLSCHAFT
    公开号:US20160280699A1
    公开(公告)日:2016-09-29
    The invention relates to substituted phenylalanine derivatives and to processes for preparation thereof, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders and/or severe perioperative blood loss.
    该发明涉及取代苯丙氨酸衍生物及其制备方法,以及其用于生产治疗和/或预防疾病的药物,特别是心血管疾病和/或严重围手术期失血的药物。
  • Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions
    作者:Anne Sophie Voisin、Alexandre Bouillon、Inmaculada Berenguer、Jean-Charles Lancelot、Aurélien Lesnard、Sylvain Rault
    DOI:10.1016/j.tet.2006.09.036
    日期:2006.12
    This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen-metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupling reactions of these novel boronic acids with selected aryl halides is described. This strategy produces novel pyridylethers of interest in cholinergic medicinal chemistry. (c) 2006 Elsevier Ltd. All rights reserved.
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