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N'-butyl-N,N-diethyl-hydrazine

中文名称
——
中文别名
——
英文名称
N'-butyl-N,N-diethyl-hydrazine
英文别名
N,N-diethylaminobutylamine;diethylaminobutylamine;2-Butyl-1,1-diethylhydrazine
<i>N</i>'-butyl-<i>N</i>,<i>N</i>-diethyl-hydrazine化学式
CAS
——
化学式
C8H20N2
mdl
——
分子量
144.26
InChiKey
OWAVWAAFOIPOIO-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
  • 重原子数:
    10
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    15.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    7-(3,5-dimethoxy-phenyl)-5-ethyl-3-methylsulfanyl-5H-pyrido[2,3-e]-1,2,4-triazin-6-oneN'-butyl-N,N-diethyl-hydrazine 以318 mg (83%)的产率得到3-(4-diethylamino-butylamino)-7-(3,5-dimethoxy-phenyl)-5-ethyl-5H-pyrido[2,3-e]-1,2,4-triazin-6-one
    参考文献:
    名称:
    Pyridotriazines and pyridopyridazines
    摘要:
    本发明涉及双环杂环,其抑制细胞周期蛋白依赖性激酶或酪氨酸激酶酶活性,或两者均有作用,因此可用于治疗细胞增殖性疾病,如血管生成、动脉粥样硬化、再狭窄和癌症,以及免疫性疾病,如哮喘、类风湿性关节炎、自身免疫性糖尿病和哺乳动物移植手术相关的移植排斥。
    公开号:
    US20020061865A1
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文献信息

  • 6-Aryl pyrido\x9b2,3-d! pyrimidines and naphthyridines for inhibiting
    申请人:——
    公开号:US05733913A1
    公开(公告)日:1998-03-31
    6-Aryl pyrido\x9b2,3-d!pyrimidines and naphthyridines are inhibitors of protein tyrosine kinase, and are thus useful in treating cellular proliferation mediated thereby. The compounds are especially useful in treating atherosclerosis, restenosis, psoriasis, as well as bacterial infections.
    6-芳基吡啶并[2,3-d]嘧啶嘧啶蛋白酪氨酸激酶抑制剂,因此在治疗由此介导的细胞增殖方面非常有用。这些化合物在治疗动脉粥样硬化、再狭窄、牛皮癣以及细菌感染方面特别有用。
  • MODULATORS OF ACETYL-COENZYME A CARBOXYLASE AND METHODS OF USE THEREOF
    申请人:Anderson Richard
    公开号:US20080200461A1
    公开(公告)日:2008-08-21
    The present invention provides compounds of formula I: along with methods of use thereof for the control of agricultural pests, particularly fungal pests, weedy pests and insect pests, as well as use as pharmaceuticals, particularly the treatment of obesity, metabolic syndrome, atherosclerosis, cardiovascular disease and insulin resistance, e.g., type II or adult-onset diabetes as well as fungal pathogens of humans and animals
    本发明提供了公式I的化合物: 以及使用它们控制农业害虫的方法,尤其是真菌害虫、杂草害虫和昆虫害虫,以及用作药物,特别是治疗肥胖、代谢综合征、动脉硬化、心血管疾病和胰岛素抵抗的方法,例如II型或成年发病型糖尿病以及人类和动物的真菌病原体。
  • Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
    申请人:——
    公开号:US20040044012A1
    公开(公告)日:2004-03-04
    This invention provides bicyclic heterocycles that are useful for treating cell proliferative disorders, such as cancer and restenosis, as well as angiogenesis and atherosclerosis. We have now discovered a group of bicyclic compounds that are potent inhibitors of cyclin-dependent kinases (cdks), growth factor-mediated kinases, and non-receptor kinases. The compounds are readily synthesized and can be administered by a variety of routes, including orally, and have sufficient bioavailability for clinical use. This invention provides compounds of Formula I: 1 where Z is N or CH; G is N or CH; W is NH, S, SO, or SO 2 , R 1 includes phenyl and substituted phenyl, R 2 includes alkyl and cycloalkyl, R 3 includes alkyl and hydrogen, R 8 and R 9 include hydrogen and alkyl, and the pharmaceutically acceptable salts thereof. This invention also provides pharmaceutical formulations comprising a compound of Formula I together with a pharmaceutically acceptable carrier, diluent, or excipient therefor.
    本发明提供了一种双环杂环化合物,用于治疗细胞增殖紊乱,如癌症和再狭窄,以及血管生成和动脉粥样硬化。我们已经发现了一组双环化合物,它们是周期蛋白依赖性激酶(cdks)、生长因子介导的激酶和非受体激酶的强效抑制剂。这些化合物易于合成,可以通过包括口服在内的多种途径给药,并且具有足够的生物利用度,适用于临床使用。本发明提供的化合物如公式I所示: 1 其中 Z是N或CH; G是N或CH; W是NH、S、SO或SO2; R1包括苯基和取代苯基, R2包括烷基和环烷基, R3包括烷基和氢, R8和R9包括氢和烷基,以及药用可接受的盐。 本发明还提供了包含公式I化合物的药物制剂,以及药用可接受的载体、稀释剂或辅料。
  • PIGMENT DISPERSING AGENT, PIGMENT COMPOSITION, AND PIGMENT COLORING AGENT
    申请人:DAINICHISEIKA COLOR & CHEMICALS MFG. CO., LTD.
    公开号:US20200377480A1
    公开(公告)日:2020-12-03
    The present invention provides a pigment dispersant: that is capable of remarkably ameliorating fluidity of a liquid product, such as an ink or a paint, which contains particles of a pigment, such as a black azo pigment, in a dispersed state; that can suppress aggregation of piment particles; that prevents occurrence of foreign substances; and that is capable of producing a colored article excellent in optical density. Provided is a pigment dispersant being a compound represented by the following formula (1). wherein R 1 and R 2 each independently represent a group obtained by eliminating one hydrogen atom from an amino group of an amine compound containing a basic nitrogen atom, and R 3 and R 4 each independently represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, or a hydroxy group.
    本发明提供了一种颜料分散剂:能够显著改善液体产品(如墨或油漆)的流动性,其中液体产品中包含颜料颗粒(如黑色偶氮颜料)处于分散状态;能够抑制颜料颗粒的聚集;防止异物的发生;并能够生产具有优异光密度的彩色制品。提供的颜料分散剂是由以下化学式(1)表示的化合物,其中R1和R2分别独立表示通过从含有碱性氮原子的胺化合物的基中消除一个氢原子而获得的基团,而R3和R4分别独立表示氢原子、卤素原子、烷基、烷氧基或羟基。
  • METHOD FOR CONTINUOUSLY PRODUCING ALKYLAMINO(METH)ACRYLAMIDES
    申请人:Schmitt Bardo
    公开号:US20110313195A1
    公开(公告)日:2011-12-22
    The invention relates to a process for continuously preparing N-alkyl(meth)acrylamides by reacting alkyl (meth)acrylates with high-boiling amines. A catalyst activation and specific workup technique achieve product qualities which have not been achieved to date. In addition, very high space-time yields and overall yields can be achieved.
    本发明涉及一种通过将烷基(甲基)丙烯酸酯与高沸点胺反应来连续制备N-烷基(甲基)丙烯酰胺的工艺。通过催化剂激活和特定的后处理技术,可以实现迄今为止未曾达到的产品质量。此外,还可以实现非常高的空间时间收率和总收率。
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