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tert-butyl (quinolin-6-ylmethyl)carbamate | 1314538-89-0

中文名称
——
中文别名
——
英文名称
tert-butyl (quinolin-6-ylmethyl)carbamate
英文别名
tert-butyl N-(quinolin-6-ylmethyl)carbamate
tert-butyl (quinolin-6-ylmethyl)carbamate化学式
CAS
1314538-89-0
化学式
C15H18N2O2
mdl
——
分子量
258.32
InChiKey
PDOFAJLQUULGTI-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:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    51.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    tert-butyl (quinolin-6-ylmethyl)carbamate盐酸 、 sodium hydride 、 potassium carbonate 作用下, 以 四氢呋喃1,4-二氧六环二氯甲烷二甲基亚砜 为溶剂, 反应 23.5h, 生成 6-(2-hydroxy-2-methylpropoxy)-4-(6-(methyl(quinolin-6-ylmethyl)amino)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile
    参考文献:
    名称:
    PYRAZOLO[1,5-A]PYRIDINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND COMPOSITION AND USE THEREOF
    摘要:
    The present invention relates to a pyrazolo[1,5-a]pyridine derivative, a preparation method therefor, and a composition and a use thereof. Specifically, the present invention relates to the compound of formula (I) and the use thereof for the treatment and/or prevention of wild type, gene-fusion type (including but not limited to KIF5B, CCDC6 and NCOA4) and mutant type (including but not limited to V804, G810 and M918) RET kinases-related diseases, including diseases or conditions mediated by RET kinase.
    公开号:
    US20230159523A1
  • 作为产物:
    描述:
    二碳酸二叔丁酯 在 potassium hydrogen bifluoride 、 palladium diacetate 、 双(三甲基硅烷基)氨基钾potassium carbonate2-二环己基磷-2,4,6-三异丙基联苯 作用下, 以 四氢呋喃甲醇甲苯 为溶剂, 反应 25.25h, 生成 tert-butyl (quinolin-6-ylmethyl)carbamate
    参考文献:
    名称:
    Synthesis and Suzuki–Miyaura Cross-Coupling Reactions of Potassium Boc-Protected Aminomethyltrifluoroborate with Aryl and Hetaryl Halides
    摘要:
    Potassium Boc-protected aminomethyltrifluoroborate, a primary aminomethyl equivalent, was synthesized successfully through a "one-pot" process. With this trifluoroborate, Suzuki-Miyaura cross-coupling reactions were investigated with a variety of both aryl and hetaryl chlorides in good to excellent yields.
    DOI:
    10.1021/ol2014768
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文献信息

  • Suzuki–Miyaura Cross-Coupling Reactions of Potassium Boc-Protected Aminomethyltrifluoroborate with Aryl and Hetaryl Mesylates
    作者:Gary A. Molander、Inji Shin
    DOI:10.1021/ol301221p
    日期:2012.6.15
    Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions were studied with potassium Boc-protected aminomethyltrifluoroborate through C-O activation of various mesylate derivatives to afford the corresponding products in moderate to good yields.
  • Pd-Catalyzed Suzuki–Miyaura Cross-Coupling Reactions between Sulfamates and Potassium Boc-Protected Aminomethyltrifluoroborates
    作者:Gary A. Molander、Inji Shin
    DOI:10.1021/ol401021x
    日期:2013.5.17
    Sulfamates were studied as the electrophilic partners in the palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with potassium Boc-protected primary and secondary aminomethyltrifluoroborates. A broad range of substrates was successfully coupled to provide the desired products. Complex molecules containing a new carbon-carbon bond and an aminomethyl moiety could be prepared through this developed method.
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