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N-[2-(二甲氨基)乙基]-2-苯基乙酰胺 | 63224-23-7

中文名称
N-[2-(二甲氨基)乙基]-2-苯基乙酰胺
中文别名
N-[2-(二甲基氨基)乙基]-苯乙酰胺
英文名称
N-[2-(dimethylamino)ethyl]-2-phenylacetamide
英文别名
phenyl-acetic acid-(2-dimethylamino-ethylamide);Phenyl-essigsaeure-(2-dimethylamino-aethylamid);Acetamide, N-(2-(dimethylamino)ethyl)-2-phenyl-
N-[2-(二甲氨基)乙基]-2-苯基乙酰胺化学式
CAS
63224-23-7
化学式
C12H18N2O
mdl
MFCD01670646
分子量
206.288
InChiKey
SKGYVELDSNNACR-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:
    377.3±35.0 °C(Predicted)
  • 密度:
    1.023±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.416
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:29bb8c551aefaaaf6d441cfa7cbf0c43
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反应信息

  • 作为产物:
    描述:
    N-cyclohexyl-2-phenyl-acetamidine; hydrochloride 在 sodium hydroxide硝基苯 作用下, 生成 N-[2-(二甲氨基)乙基]-2-苯基乙酰胺
    参考文献:
    名称:
    174. Am。第十三部分。由取代的am和亚烷基二胺制备2-取代的4:5-二氢乙二醛和环同系物
    摘要:
    DOI:
    10.1039/jr9500000859
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文献信息

  • A convenient synthesis of amides from carboxylic acids and primary amines
    作者:J. Cossy、C. Pale-Grosdemange
    DOI:10.1016/s0040-4039(00)99121-4
    日期:1989.1
    A convenient method for the formation of carboxamides from carboxylic acids and primary amines in the presence of molecular sieves is described. This process is very chemoselective.
    描述了一种在分子筛存在下由羧酸和伯胺形成羧酰胺的简便方法。这个过程是非常化学选择性的。
  • Anti-inflammatory 1-phenylethanolamine derivatives, pharmaceutical compositions thereof and processes for their manufacture
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0000809A1
    公开(公告)日:1979-02-21
    The invention relates to topically anti-inflammatory 1-phenylethanolamine derivatives of the general formula I:- or acid-addition salts thereof, to pharmaceutical compositions thereof, and to analogy processes for their manufacture. A representative compound is 1-(4-amino -3,5- dichlorophenyl) -2- [1,1-dimethyl -2- (2-phenylacetamido) ethylamino] ethanol. The derivatives are useful in particular for the treatment of inflammatory diseases or conditions of the akin.
    本发明涉及通式 I:- 的局部抗炎 1-苯基乙醇胺衍生物或其酸加成盐,涉及其药物组合物,涉及其生产的类比工艺。 一个代表性的化合物是 1-(4-氨基-3,5-二氯苯基)-2-[1,1-二甲基-2-(2-苯基乙酰氨基)乙基氨基]乙醇。 这些衍生物特别适用于治疗炎症性疾病或类似疾病。
  • Designing Anti-inflammatory Drugs from Parasitic Worms: A Synthetic Small Molecule Analogue of the <i>Acanthocheilonema viteae</i> Product ES-62 Prevents Development of Collagen-Induced Arthritis
    作者:Lamyaa Al-Riyami、Miguel A. Pineda、Justyna Rzepecka、Judith K. Huggan、Abedawn I. Khalaf、Colin J. Suckling、Fraser J. Scott、David T. Rodgers、Margaret M. Harnett、William Harnett
    DOI:10.1021/jm401251p
    日期:2013.12.27
    In spite of increasing evidence that parasitic worms may protect humans from developing allergic and autoimmune diseases and the continuing identification of defined helminth-derived immunomodulatory molecules, to date no new anti-inflammatory drugs have been developed from these organisms. We have approached this matter in a novel manner by synthesizing a library of drug-like small molecules based upon phosphorylcholine, the active moiety of the anti-inflammatory Acanthocheilonema viteae product, ES-62, which as an immunogenic protein is unsuitable for use as a drug. Following preliminary in vitro screening for inhibitory effects responses, a sulfone-containing phosphorylcholine analogue (11a) was selected for testing in collagen-induced arthritis (CIA). Testing revealed that 11a was as effective as ES-62 in protecting DBA/1 mice from developing CIA and mirrored its mechanism of action in downregulating the TLR/IL-1R transducer, MyD88. 11a is thus a novel prototype for anti-inflammatory drug development. on relevant macrophage cytokine an in vivo model of inflammation,
  • HETEROCYCLIC COMPOUNDS, MEDICAMENTS CONTAINING SAID COMPOUNDS, USE THEREOF AND PROCESSES FOR THE PREPARATION THEREOF
    申请人:Boehringer Ingelheim International GmbH
    公开号:EP2794595B1
    公开(公告)日:2017-08-02
  • 174. Amidines. Part XIII. Preparation of 2-substituted 4 : 5-dihydroglyoxalines and ring homologues from substituted amidines and alkylenediamines
    作者:P. Oxley、W. F. Short
    DOI:10.1039/jr9500000859
    日期:——
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐