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5-Bromo-3-p-tolyl-pyrazin-2-ylamine | 625848-15-9

中文名称
——
中文别名
——
英文名称
5-Bromo-3-p-tolyl-pyrazin-2-ylamine
英文别名
5-bromo-3-(4-methylphenyl)pyrazin-2-amine
5-Bromo-3-p-tolyl-pyrazin-2-ylamine化学式
CAS
625848-15-9
化学式
C11H10BrN3
mdl
——
分子量
264.124
InChiKey
UKCMRYLUHFUALE-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

  • 熔点:
    118-120 °C
  • 沸点:
    355.8±37.0 °C(Predicted)
  • 密度:
    1.501±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    51.8
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    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:
    5-Bromo-3-p-tolyl-pyrazin-2-ylamine盐酸二(氰基苯)二氯化钯sodium carbonate1,4-双(二苯基膦)丁烷 作用下, 以 1,4-二氧六环乙醇甲苯 为溶剂, 反应 5.12h, 生成 2-(4-hydroxybenzyl)-6-(4-hydroxyphenyl)-8-(4-methylphenyl)imidazo[1,2-a]pyrazin-3(7H)-one
    参考文献:
    名称:
    Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties
    摘要:
    A series of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones were prepared from 2-amino-3,5-dibromopyrazine. The concise synthesis of coelenterazine (5j), in three steps, 48% overall yield and >99% purity exemplifies the strategy. Further, the synthetic approach facilitated the regiospecific incorporation of carboxyalkyl linkers on the 3,7-dihydroimidazo[1,2a]pyrazine-3-one nucleus that are required for bioconjugation. Peroxymonocarbonate, an electrophilic oxidant, was used to initiate 'pseudo-flash' chemiluminescence from this class of molecules. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2003.08.040
  • 作为产物:
    描述:
    4-甲苯硼酸2-氨基-3,5-二溴吡嗪二(氰基苯)二氯化钯sodium carbonate1,4-双(二苯基膦)丁烷 作用下, 以 乙醇甲苯 为溶剂, 反应 7.0h, 以38%的产率得到5-Bromo-3-p-tolyl-pyrazin-2-ylamine
    参考文献:
    名称:
    Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties
    摘要:
    A series of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones were prepared from 2-amino-3,5-dibromopyrazine. The concise synthesis of coelenterazine (5j), in three steps, 48% overall yield and >99% purity exemplifies the strategy. Further, the synthetic approach facilitated the regiospecific incorporation of carboxyalkyl linkers on the 3,7-dihydroimidazo[1,2a]pyrazine-3-one nucleus that are required for bioconjugation. Peroxymonocarbonate, an electrophilic oxidant, was used to initiate 'pseudo-flash' chemiluminescence from this class of molecules. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2003.08.040
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文献信息

  • NEW ANTI-MALARIAL AGENTS
    申请人:UNIVERSITY OF CAPE TOWN
    公开号:US20180194741A1
    公开(公告)日:2018-07-12
    The present invention is related to a use of aminopyrazine derivatives in the manufacture of a medicament for preventing or treating malaria. Specifically, the present invention is related to aminopyrazine derivatives useful for the preparation of a pharmaceutical formulation for the inhibition of malaria parasite proliferation.
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