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1-对甲苯基-4,5-二氢-1H-吡唑 | 34946-99-1

中文名称
1-对甲苯基-4,5-二氢-1H-吡唑
中文别名
——
英文名称
1-(p-tolyl)-4,5-dihydro-1H-pyrazole
英文别名
1-P-Tolyl-4,5-dihydro-1H-pyrazole;2-(4-methylphenyl)-3,4-dihydropyrazole
1-对甲苯基-4,5-二氢-1H-吡唑化学式
CAS
34946-99-1
化学式
C10H12N2
mdl
MFCD09032133
分子量
160.219
InChiKey
ORDKRLFWJUCKCT-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:
    277.6±33.0 °C(Predicted)
  • 密度:
    1.06±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    15.6
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933199090

SDS

SDS:017e51379bdf77277ab7775396be300c
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反应信息

  • 作为反应物:
    描述:
    1-对甲苯基-4,5-二氢-1H-吡唑乙醇 、 alkaline earth salt of/the/ methylsulfuric acid 生成 N-(3-aminopropyl)-p-toluidine
    参考文献:
    名称:
    Balbiano, Gazzetta Chimica Italiana, 1888, vol. 18, p. 358
    摘要:
    DOI:
  • 作为产物:
    描述:
    N-3-Brompropyl-p-toluidin 在 iron(III) chloride 、 sodium azide 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 80.0~100.0 ℃ 、101.33 kPa 条件下, 反应 13.0h, 生成 1-对甲苯基-4,5-二氢-1H-吡唑
    参考文献:
    名称:
    Fe(III)-Catalyzed Aerobic Intramolecular N–N Coupling of Aliphatic Azides with Amines
    摘要:
    An Fe(III)-catalyzed intramolecular N-N coupling of aliphatic azidoamines that forms diverse five-and six-membered semisaturated diazoheterocycles using air as an oxidant is reported, providing an alternative to hydrazine-based methods. Mechanistic studies suggest that a N-radical induced intramolecular homolytic substitution (S(H)2) is involved in ring closure. The power of this N-N bond-forming method is also demonstrated by using it as the final step in a total synthesis of (-)-newbouldine.
    DOI:
    10.1021/acs.orglett.9b01396
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文献信息

  • Microwave-assisted cyclocondensation of hydrazine derivatives with alkyl dihalides or ditosylates in aqueous media: syntheses of pyrazole, pyrazolidine and phthalazine derivatives
    作者:Yuhong Ju、Rajender S. Varma
    DOI:10.1016/j.tetlet.2005.07.018
    日期:2005.9
    Direct syntheses of 4,5-dihydro-pyrazole, pyrazolidine, and 1,2-dihydro-phthalazine derivatives via double-alkylation of hydrazines by alkyl dihalides or ditosylates were accomplished in aqueous media under microwave irradiation conditions; the environmentally friendlier chemical transformation occurred in a single step and eliminated the use of expensive metal catalysts in building two C–N bonds.
    在微波辐射条件下,在含水介质中,通过烷基二卤化物或二甲苯磺酸盐对肼的双烷基化反应,直接合成4,5-二氢吡唑,吡唑烷和1,2-二氢邻苯二甲酰肼衍生物。有利于环境的化学转化过程一步完成,消除了使用昂贵的金属催化剂来构建两个C–N键的过程。
  • Ruthenium-Catalyzed Divergent Acceptorless Dehydrogenative Coupling of 1,3-Diols with Arylhydrazines: Synthesis of Pyrazoles and 2-Pyrazolines
    作者:Yanling Zheng、Yang Long、Huihua Gong、Jiaqi Xu、Chunchun Zhang、Haiyan Fu、Xueli Zheng、Hua Chen、Ruixiang Li
    DOI:10.1021/acs.orglett.2c01497
    日期:2022.6.3
    1,3-diols with arylhydrazines via acceptorless dehydrogenative coupling reactions to selectively synthesize pyrazoles and 2-pyrazolines were reported, which were based on Ru3(CO)12/NHC-phosphine-phosphine catalytic systems. The reactions featured low catalyst loading, high selectivity, wide substrate scope, and good yields, with only water and hydrogen gas (H2) as the byproducts.
    本文报道了基于Ru 3 (CO) 12 /NHC-膦-膦催化体系的1,3-二醇与芳基肼通过无受体脱氢偶联反应选择性合成吡唑和2-吡唑啉的不同转化。该反应具有催化剂负载量低、选择性高、底物范围广、收率高的特点,仅副产物水和氢气(H 2 )。
  • Aqueous N-Heterocyclization of Primary Amines and Hydrazines with Dihalides:  Microwave-Assisted Syntheses of <i>N</i>-Azacycloalkanes, Isoindole, Pyrazole, Pyrazolidine, and Phthalazine Derivatives
    作者:Yuhong Ju、Rajender S. Varma
    DOI:10.1021/jo051878h
    日期:2006.1.1
    The synthesis of nitrogen-containing heterocycles from alkyl dihalides (ditosylates) and primary amines and hydrazines via a simple and efficient cyclocondensation in an alkaline aqueous medium that occurs under microwave irradiation is described. This improved greener synthetic methodology provides a simple C C and straightforward one-pot approach to the synthesis of a variety of heterocycles, such as substituted azetidines, pyrrolidines, piperidines, azepanes, N-substituted 2,3-diliydro-1H-isoindoles. 4,5-dihydropyrazoles, pyrazolidines, and 1,2-dihydrophthalazines.
  • Facile Synthesis of 1-Arylpyrazoles
    作者:Yiwen Yang、Chunxiang Kuang
    DOI:10.1055/s-0034-1380658
    日期:——
    A convenient and transition-metal-free synthesis of 1-arylpyrazoles that involves the cycloaddition of 3-arylsydnones and acrylic acid is presented. The process proceeds smoothly to obtain the target products with moderate to high yields.
  • US9611230B2
    申请人:——
    公开号:US9611230B2
    公开(公告)日:2017-04-04
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同类化合物

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