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3-amino-quinolin-4-ol; hydrochloride | 129377-66-8

中文名称
——
中文别名
——
英文名称
3-amino-quinolin-4-ol; hydrochloride
英文别名
3-Amino-chinolin-4-ol; Hydrochlorid;3-aminoquinolin-4-ol hydrochloride;3-amino-1H-quinolin-4-one;hydrochloride
3-amino-quinolin-4-ol; hydrochloride化学式
CAS
129377-66-8
化学式
C9H8N2O*ClH
mdl
——
分子量
196.636
InChiKey
IDYWCCVZUREPCI-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):
    1.53
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    55.1
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-amino-quinolin-4-ol; hydrochloride盐酸 、 sodium nitrite 作用下, 生成 4(3H)-喹啉酮,3-重氮基-
    参考文献:
    名称:
    Sues et al., Justus Liebigs Annalen der Chemie, 1953, vol. 583, p. 150,155
    摘要:
    DOI:
  • 作为产物:
    描述:
    3-硝基-4-羟基喹啉 以60%的产率得到
    参考文献:
    名称:
    PONOMAREV, O. A.;BRUSILTSEV, YU. N.;GRIF, V. X.;MITINA, V. G., YKP. XIM. ZH., 56,(1990) N, S. 272-276
    摘要:
    DOI:
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文献信息

  • Oxazolo, thiazolo and selenazolo [4,5-c]-quinolin-4-amines and analogs
    申请人:3M Innovative Properties Company
    公开号:US06110929A1
    公开(公告)日:2000-08-29
    Thiazolo-, oxazolo- and selenazolo[4,5-c]quinolin-4-amines and analogs thereof are described including methods of manufacture and the use of novel intermediates. The compounds are immunomodulators and induce cytokine biosynthesis, including interferon and/or tumor biosynthesis, necrosis factor, and inhibit the T-helper-type 2 immune response. The compounds are further useful in the treatment of viral and neoplastic diseases.
    Thiazolo-, oxazolo-和selenazolo[4,5-c]quinolin-4-胺及其类似物的描述包括制造方法和新型中间体的使用。这些化合物是免疫调节剂,能诱导细胞因子生物合成,包括干扰素和/或肿瘤生物合成、坏死因子,并抑制T辅助型2型免疫应答。这些化合物在治疗病毒性和肿瘤性疾病方面也很有用。
  • Oxazolo, thiazolo and selenazolo [4,5-c]-quinolin-4- amines and analogs thereof
    申请人:3M Innovative Properties Company
    公开号:US20030195224A1
    公开(公告)日:2003-10-16
    Thiazolo-, oxazolo- and selenazolo[4,5-c]quinolin-4-amines and analogs thereof are described including methods of manufacture and the use of novel intermediates. The compounds are immunomodulators and induce cytokine biosynthesis, including interferon and/or tumor biosynthesis, necrosis factor, and inhibit the T-helper-type 2 immune response. The compounds are further useful in the treatment of viral and neoplastic diseases.
    本文描述了噻唑啉、噁唑啉和硒唑啉[4,5-c]喹啉-4-胺及其类似物,包括制造方法和新型中间体的用途。这些化合物是免疫调节剂,可诱导细胞因子生物合成,包括干扰素和/或肿瘤生物合成、坏死因子,并抑制T辅助型2免疫反应。这些化合物还可用于治疗病毒和肿瘤性疾病。
  • Oxazolo, thiazolo and selenazolo [4,5-c]-quinolin-4-amines and analogs thereof
    申请人:3M Innovative Properties Company
    公开号:US20030045545A1
    公开(公告)日:2003-03-06
    Thiazolo-, oxazolo- and selenazolo[4,5-c]quinolin-4-amines and analogs thereof are described including methods of manufacture and the use of novel intermediates. The compounds are immunomodulators and induce cytokine biosynthesis, including interferon and/or tumor biosynthesis, necrosis factor, and inhibit the T-helper-type 2 immune response. The compounds are further useful in the treatment of viral and neoplastic diseases.
    本文描述了噻唑-、噁唑-和硒唑- [4,5-c]喹啉-4-胺及其类似物,包括制造方法和新型中间体的用途。这些化合物是免疫调节剂,可诱导细胞因子生物合成,包括干扰素和/或肿瘤生物合成、坏死因子,并抑制T-helper型2免疫反应。此外,这些化合物还可用于治疗病毒和肿瘤性疾病。
  • Oxazolo, thiazolo and selenazolo [4,5-C]-quinolin-4-amines and analogs thereof
    申请人:3M Innovative Properties Company
    公开号:US06809203B2
    公开(公告)日:2004-10-26
    Thiazolo-, oxazolo- and selenazolo[4,5-c]quinolin-4-amines and analogs thereof are described including methods of manufacture and the use of novel intermediates. The compounds are immunomodulators and induce cytokine biosynthesis, including interferon and/or tumor biosynthesis, necrosis factor, and inhibit the T-helper-type 2 immune response. The compounds are further useful in the treatment of viral and neoplastic diseases.
    本文描述了噻唑并吡唑、氧唑并吡唑和硒唑并[4,5-c]喹啉-4-胺及其类似物,包括其制造方法和新型中间体的使用。这些化合物是免疫调节剂,可诱导细胞因子的生物合成,包括干扰素和/或肿瘤坏死因子,并抑制T辅助型2型免疫应答。此外,这些化合物还可用于治疗病毒和肿瘤性疾病。
  • Method for 1H-Imidazo[4,5-C] Pyridines and Analogs Thereof
    申请人:Krepski Larry R.
    公开号:US20090240055A1
    公开(公告)日:2009-09-24
    Methods and intermediates for preparing compounds of the Formulas: (I and X) are disclosed. The methods include a method providing a compound of the Formula: (IV) and converting a compound of Formula IV to a compound of Formula I, a method providing a compound of the Formula: (VIII) and converting a compound of Formula VIII to a compound of Formula I, and a method providing a compound of the Formula: (XI) and converting a compound of Formula XI to a compound of Formula I.
    本文揭示了制备化合物公式(I和X)的方法和中间体。这些方法包括提供公式(IV)化合物并将公式IV化合物转化为公式I化合物的方法,提供公式(VIII)化合物并将公式VIII化合物转化为公式I化合物的方法,以及提供公式(XI)化合物并将公式XI化合物转化为公式I化合物的方法。
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