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N,N-二甲基-6-苯基甲氧基-1-苯并噻吩-2-胺 | 193965-55-8

中文名称
N,N-二甲基-6-苯基甲氧基-1-苯并噻吩-2-胺
中文别名
——
英文名称
6-benzyloxy-2-(dimethyl-amino)benzo[b]thiophene
英文别名
2-dimethylamino-6-benzyloxybenzothiophene;2-dimethylamino-6-benzyloxybenzo[b]thiophene;6-benzyloxy-2-(dimethylamino)benzo[b]thiophene;6-benzyloxy-2-dimethylaminobenzo[b]thiophene;N,N-dimethyl-6-phenylmethoxy-1-benzothiophen-2-amine
N,N-二甲基-6-苯基甲氧基-1-苯并噻吩-2-胺化学式
CAS
193965-55-8
化学式
C17H17NOS
mdl
——
分子量
283.394
InChiKey
GKAJJEOXDGDXKG-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:
    439.1±30.0 °C(Predicted)
  • 密度:
    1.202±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    40.7
  • 氢给体数:
    0
  • 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:
    参考文献:
    名称:
    Diamino Benzo[b]thiophene Derivatives as a Novel Class of Active Site Directed Thrombin Inhibitors. 5. Potency, Efficacy, and Pharmacokinetic Properties of Modified C-3 Side Chain Derivatives
    摘要:
    A systematic investigation of the structure-activity relationships of the C-3 side chain of the screening hit la led to the identification of the potent thrombin inhibitors 23c, 28c, and 31c. Their activities (1240, 903, and 1271 x 10(6) L/mol, respectively) represent 2200- and 2900-fold increases in potency over the starting lead la. This activity enhancement was accomplished with an increase of thrombin selectivity. The in vitro anticoagulant profiles of derivatives 28c and 31c were determined, and they compare favorably with the clinical agent H-R-1-[4aS,-8aS]perhydroisoquinolyl-prolyl-arginyl aldehyde (D-Piq-Pro-Arg-H; 32). The more potent members of this series have been studied in an arterial/venous shunt (AV shunt) model of thrombosis and were found to be efficacious in reducing clot formation. However, their efficacy is currently limited by their rapid and extensive distribution following administration.
    DOI:
    10.1021/jm9903388
  • 作为产物:
    描述:
    N,N-dimethyl-2-hydroxy-2-(4-benzyloxy)phenylthioacetamide甲烷磺酸 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 1.5h, 以70%的产率得到N,N-二甲基-6-苯基甲氧基-1-苯并噻吩-2-胺
    参考文献:
    名称:
    Antithrombotic agents
    摘要:
    这项申请涉及到式(I)的新化合物(及其药用可接受的盐),如本文所定义,用于它们的制备的工艺和中间体,包括式(I)的新化合物的药物配方,以及将式(I)的化合物用作凝血酶抑制剂。
    公开号:
    US06350774B1
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文献信息

  • Antithrombotic diamines
    申请人:Eli Lilly and Company
    公开号:US06025382A1
    公开(公告)日:2000-02-15
    This application relates to the use as thrombin inhibitors, coagulation inhibitors and thromboembolic disorder agents of diamines of formula I as defined herein. It also provides novel compounds of formula I, processes and intermediates for their preparation, and pharmaceutical formulations comprising the novel compounds of formula I.
    该应用涉及将I式中所定义的二胺用作凝血酶抑制剂、凝血抑制剂和血栓栓塞性疾病药剂。它还提供了I式的新化合物,其制备方法和中间体,以及包含这些新化合物的药物配方。
  • Thrombin inhibitors
    申请人:Eli Lilly and Company
    公开号:US06391901B1
    公开(公告)日:2002-05-21
    This application relates to novel compounds of formula I (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula I, and the use of defined compounds of formula I as thrombin inhibitors.
    这项申请涉及到式I的新化合物(及其药学上可接受的盐),如本文所定义,用于它们的制备的过程和中间体,包含式I的新化合物的药物配方,以及将式I的特定化合物用作凝血酶抑制剂
  • Antithrombotic Agents
    申请人:Eli Lilly and Company
    公开号:US06271227B1
    公开(公告)日:2001-08-07
    This application relates to novel compounds of formula (I) (and their pharmaceutically acceptable salts), as defined herein, processes and intermediates for their preparation, pharmaceutical formulations comprising the novel compounds of formula (I), and the use of the compounds of formula (I) as thrombin inhibitors.
    本申请涉及公式(I)的新化合物(以及其药学上可接受的盐),如此处所定义,用于其制备的过程和中间体,含有公式(I)新化合物的制药配方,以及化合物(I)作为凝血酶抑制剂的用途。
  • [EN] ANTITHROMBOTIC DIAMINES<br/>[FR] DIAMINES ANTITHROMBOTIQUES
    申请人:ELI LILLY AND COMPANY
    公开号:WO1997025033A1
    公开(公告)日:1997-07-17
    (EN) This application relates to the use as thrombin inhibitors, coagulation inhibitors and thromboembolic disorder agents of diamines of formula (I) as defined herein. It also provides novel compounds of formula (I), processes and intermediates for their preparation, and pharmaceutical formulations comprising the novel compounds of formula (I).(FR) La présente invention concerne l'utilisation, comme inhibiteurs de thrombine, inhibiteurs de coagulation et agents destinés aux désordres de la thromboembolie, de diamines de formule I telle qu'elle est définie dans la description. L'invention concerne aussi des composés nouveaux de formule I, des procédés et des produits intermédiaires pour leur préparation, et des formulations pharmaceutiques comprenant les composés nouveaux de formule I.
    该应用涉及使用公式(I)所定义的二胺作为凝血酶抑制剂、凝血抑制剂和血栓栓塞疾病药物的用途。它还提供了公式(I)的新化合物、其制备过程和中间体,以及包含公式(I)的新药物配方。
  • Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C3-side chain of hydroxybenzo[b]thiophenes
    作者:Kumiko Takeuchi、Todd J. Kohn、Daniel J. Sall、Michael L. Denney、Jefferson R. McCowan、Gerry F. Smith、Donetta S. Gifford-Moore
    DOI:10.1016/s0960-894x(99)00076-1
    日期:1999.3
    A novel series of benzo[b]thiophene diamine thrombin inhibitors with a conformationally restricted C3-side chain 3 was investigated. The constrained C3-side chain by a cyclohexyl ring contributed to not only an additive but also a synergistic effect on the thrombin inhibitory activity. The SAR studies resulted in the discovery of a potent thrombin inhibitor 27 that was over 750-fold more potent than the initial lead compound 1. (C) 1999 Elsevier Science Ltd. All rights reserved.
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