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5-(4'-chlorophenyl)-1-methyl-1H-pyrazole | 73387-54-9

中文名称
——
中文别名
——
英文名称
5-(4'-chlorophenyl)-1-methyl-1H-pyrazole
英文别名
5-(4-chlorophenyl)-1-methylpyrazole;5-(4-chloro-phenyl)-1-methyl-1H-pyrazole;5-(p-Chlorphenyl)-1-methyl-pyrazol
5-(4'-chlorophenyl)-1-methyl-1H-pyrazole化学式
CAS
73387-54-9
化学式
C10H9ClN2
mdl
——
分子量
192.648
InChiKey
DZEQTUVULKDHJI-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

  • 沸点:
    120 °C(Press: 0.2 Torr)
  • 密度:
    1.20±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

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

  • 作为产物:
    描述:
    三氟甲磺酸-4-氯苯醚potassium 1-methyl-1H-pyrazole-5-carboxylate2,6-二甲基吡啶三苯基膦 、 silver carbonate 、 palladium dichloride 作用下, 以 N-甲基吡咯烷酮 为溶剂, 反应 16.0h, 以60%的产率得到5-(4'-chlorophenyl)-1-methyl-1H-pyrazole
    参考文献:
    名称:
    Ag / Pd催化的芳基三氟甲磺酸酯与芳族羧酸盐的低温脱羧交叉偶联
    摘要:
    在比最知名的铜催化剂低50°C的条件下,催化银(I)/钯(II)系统可在低至120°C的温度下将芳族羧酸酯与芳基三氟甲磺酸酯进行脱羧交叉偶联。值得注意的是,多氯代芳烃羧酸酯和许多杂环芳烃羧酸酯首次以高收率转化。FG =功能组。
    DOI:
    10.1002/chem.200903319
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文献信息

  • Palladium-catalysed direct diarylations of pyrazoles with aryl bromides: a one step access to 4,5-diarylpyrazoles
    作者:Abdelilah Takfaoui、Liqin Zhao、Rachid Touzani、Pierre H. Dixneuf、Henri Doucet
    DOI:10.1016/j.tetlet.2014.01.079
    日期:2014.3
    The palladium-catalysed direct arylation of pyrazoles with aryl halides, using PdCl(C3H5)(dppb)/KOAc catalyst, reveals a similar reactivity of C4 and C5 CH bonds of pyrazoles, whereas the C3 CH bond is almost unreactive, and gives access in one step to a variety of 4,5-diarylpyrazoles. This CH bond functionalisation reaction tolerates a variety of substituents on the aryl bromide such as nitro, cyano
    使用PdCl(C 3 H 5)(dppb)/ KOAc催化剂,催化吡唑与芳基卤化物的直接芳基化反应显示出吡唑的C4和C5 C H键具有相似的反应性,而C3 C H键几乎不具有反应性,并一步一步即可获得各种4,5-二芳基吡唑类化合物。该C H键官能化反应容许芳基化物上的各种取代基,例如硝基,基,甲酰基,丙酰基,酯,或三甲基。
  • PIPERIDIN-1 -YL AND AZEPIN-1 -YL CARBOXYLATES AS MUSCARINIC M4 RECEPTOR AGONISTS
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20150376179A1
    公开(公告)日:2015-12-31
    The present invention provides muscarinic M4 receptor agonists of formula (I) and pharmaceutically acceptable salts thereof, wherein m, n, p, q, R, R 2 and R 3 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases such as schizophrenia, Alzheimer's disease and various cognitive disorders as well as in the treatment or alleviation of pain.
    本发明提供公式(I)及其药学上可接受的盐的毛果碱M4受体激动剂,其中m,n,p,q,R,R2和R3如规范中所定义,其制备过程,含有它们的药物组合物以及它们在治疗诸如精神分裂症,阿尔茨海默病和各种认知障碍以及治疗或缓解疼痛方面的用途。
  • Piperidin-1-yl and azepin-1-yl carboxylates as muscarinic M4 receptor agonists
    申请人:Heptares Therapeutics Limited
    公开号:US10030012B2
    公开(公告)日:2018-07-24
    The present invention provides muscarinic M4 receptor agonists of formula (I) and pharmaceutically acceptable salts thereof, wherein m, n, p, q, R, R2 and R3 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases such as schizophrenia, Alzheimer's disease and various cognitive disorders as well as in the treatment or alleviation of pain.
    本发明提供了式 (I) 的毒蕈碱类 M4 受体激动剂及其药学上可接受的盐(其中 m、n、p、q、R、R2 和 R3 如说明书中所定义)、其制备工艺、含有它们的药物组合物以及它们在治疗诸如精神分裂症、阿尔茨海默病和各种认知障碍等疾病以及治疗或减轻疼痛中的用途。
  • Alkali-metal mediated zincation of N-heterocyclic substrates using the lithium zincate complex, (THF)Li(TMP)Zn(tBu)2 and applications in in situ cross coupling reactions
    作者:Victoria L. Blair、David C. Blakemore、Duncan Hay、Eva Hevia、David C. Pryde
    DOI:10.1016/j.tetlet.2011.06.090
    日期:2011.9
    This study investigates the ability of the mixed-metal reagent [Li(TMP)Zn(tBu)(2)] 1 to promote direct Zn-H exchange reactions (zincations) of a wide range of N-heterocyclic molecules. The generated metallated intermediates from these reactions are intercepted with I-2 and some of them are also employed as precursors in Pd-catalysed Negishi cross-coupling applications. A comparison with recent precedents in metallation chemistry reveals that for some of these heterocycles, 1 allows improved conversions, under milder conditions and in certain cases, even gives unique regioselectivities. (C) 2011 Elsevier Ltd. All rights reserved.
  • GRIMMETT M. R.; LIM K. H. R.; WEAVERS R. T., AUSTRAL. J. CHEM., 1979, 32, NO 10, 2203-2213
    作者:GRIMMETT M. R.、 LIM K. H. R.、 WEAVERS R. T.
    DOI:——
    日期:——
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