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5-iodo-2-propoxypyridine | 1363437-95-9

中文名称
——
中文别名
——
英文名称
5-iodo-2-propoxypyridine
英文别名
——
5-iodo-2-propoxypyridine化学式
CAS
1363437-95-9
化学式
C8H10INO
mdl
——
分子量
263.078
InChiKey
DVPWKLJJCUBQET-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):
    2.7
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    5-iodo-2-propoxypyridineN-(quinolin-8-yl)butyramide 在 palladium diacetate 、 磷酸二丁酯 、 silver carbonate 、 sodium iodide 作用下, 以 N,N-二甲基乙酰胺甲苯 为溶剂, 反应 24.0h, 以67%的产率得到
    参考文献:
    名称:
    Synthesis of Alkyl-Substituted Pyridines by Directed Pd(II)-Catalyzed C–H Activation of Alkanoic Amides
    摘要:
    A general alkylation protocol for substituted iodopyridines was developed (32 examples, 44-97% yield). The reaction is based on the Pd(II)-catalyzed C-H activation of 8-aminoquinoline-derived alkanoic amides and it employs a catalyst cocktail of Pd(OAc)(2) (10 mol%), NaI (30 mol%), and (BuO)(2)POOH (20 mol%), with Ag2CO3 as base.
    DOI:
    10.1055/s-0035-1560810
  • 作为产物:
    描述:
    2-羟基-5-碘吡啶1-碘代丙烷 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 21.0h, 以34%的产率得到5-iodo-2-propoxypyridine
    参考文献:
    名称:
    Synthesis of Alkyl-Substituted Pyridines by Directed Pd(II)-Catalyzed C–H Activation of Alkanoic Amides
    摘要:
    A general alkylation protocol for substituted iodopyridines was developed (32 examples, 44-97% yield). The reaction is based on the Pd(II)-catalyzed C-H activation of 8-aminoquinoline-derived alkanoic amides and it employs a catalyst cocktail of Pd(OAc)(2) (10 mol%), NaI (30 mol%), and (BuO)(2)POOH (20 mol%), with Ag2CO3 as base.
    DOI:
    10.1055/s-0035-1560810
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文献信息

  • [EN] ETHYNE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF<br/>[FR] DÉRIVÉS D'ÉTHYNE, COMPOSITIONS PHARMACEUTIQUES ET LEURS UTILISATIONS
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2012032014A1
    公开(公告)日:2012-03-15
    invention relates to new compounds of the formula I to their use as medicaments, to methods for their therapeutic use and to pharmaceutical compositions containing them.
    这项发明涉及公式I的新化合物,涉及它们作为药物的用途,涉及它们的治疗用途的方法,以及含有它们的药物组合物。
  • New compounds, pharmaceutical compositions and uses thereof
    申请人:ROTH Gerald Juergen
    公开号:US20120214782A1
    公开(公告)日:2012-08-23
    The invention relates to new compounds of the formula I to their use as medicaments, to methods for their therapeutic use and to pharmaceutical compositions containing them.
    这项发明涉及公式I的新化合物,以及它们作为药物的用途,它们的治疗用途的方法,以及含有它们的药物组合物。
  • [EN] ALKYNE COMPOUNDS AS S-NITROSOGLUTATHIONE REDUCTASE INHIBITORS<br/>[FR] COMPOSÉS DE TYPE ALCYNE EN TANT QU'INHIBITEURS DE LA S-NITROSOGLUTATHIONE RÉDUCTASE
    申请人:GLENMARK PHARMACEUTICALS SA
    公开号:WO2016055947A1
    公开(公告)日:2016-04-14
    Provided are compounds of formula (Ia) and pharmaceutically acceptable salts thereof, wherein A, B, R 1, R 2, m and n are as defined herein, which are active as inhibitors of S-Nitrosoglutathione reductase (GSNOR). These compounds prevent, inhibit, or suppress the action of GSNOR and are therefore useful in the treatment of GSNOR mediated diseases, disorders, syndromes or conditions such as, e.g., pulmonary hypertension, acute respiratory distress syndrome (ARDS), asthma, bronchospasm, cough, pneumonia, pulmonary fibrosis, interstitial lung diseases, cystic fibrosis and chronic obstructive pulmonary disease (COPD).
    提供的是式(Ia)的化合物及其药学上可接受的盐,其中A、B、R1、R2、m和n如本文所定义,这些化合物作为S-硝基谷胱甘肽还原酶(GSNOR)的抑制剂具有活性。这些化合物可以预防、抑制或抑制GSNOR的作用,因此在治疗GSNOR介导的疾病、疾病、综合征或病症方面具有用处,例如肺动脉高压、急性呼吸窘迫综合征(ARDS)、哮喘、支气管痉挛、咳嗽、肺炎、肺纤维化、间质性肺疾病、囊性纤维化和慢性阻塞性肺疾病(COPD)。
  • [EN] NEW COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF<br/>[FR] NOUVEAUX COMPOSÉS, COMPOSITIONS PHARMACEUTIQUES, ET LEURS UTILISATIONS
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2012028676A1
    公开(公告)日:2012-03-08
    The invention relates to new compounds of the formula (I) to their use as medicaments, to methods for their therapeutic use and to pharmaceutical compositions containing them.
    该发明涉及公式(I)的新化合物,以及它们作为药物的用途,用于它们的治疗用途的方法以及含有它们的药物组合物。
  • SUBSTITUTED HETEROARYL- AND ARYLALKYNYL BENZENE DERIVATIVES AS ACC-INHIBITORS FOR THE TREATMENT OF METABOLIC DISEASES
    申请人:Boehringer Ingelheim International GmbH
    公开号:EP2611771B1
    公开(公告)日:2016-11-23
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