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2-amino-3-cyano-4-thenylaminoquinoline | 477708-42-2

中文名称
——
中文别名
——
英文名称
2-amino-3-cyano-4-thenylaminoquinoline
英文别名
2-amino-4-(thiophen-2-ylmethylamino)quinoline-3-carbonitrile
2-amino-3-cyano-4-thenylaminoquinoline化学式
CAS
477708-42-2
化学式
C15H12N4S
mdl
——
分子量
280.353
InChiKey
LELCQSVSHYQGMI-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):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    103
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2-amino-3-cyano-4-thenylaminoquinoline3-溴丙酮酸乙酯乙醇 为溶剂, 反应 2.0h, 生成 ethyl 9-thenylamino-10-cyanoimidazo[1,2-a]quinoline-2-carboxylate
    参考文献:
    名称:
    [EN] IMIDAZOQUINOLINE DERIVATIVES AS ADENOSINE A3 RECEPTOR LIGANDS
    [FR] DERIVES D'IMIDAZOQUINOLINE EN TANT QUE LIGANDS RECEPTEURS DE L'ADENOSINE A3
    摘要:
    通式(I)的化合物,其中X,Z,R1-R10,m,n,o,p,r如说明中所述,是强的腺苷A3受体配体,最好是拮抗剂。
    公开号:
    WO2004046146A1
  • 作为产物:
    描述:
    2-噻吩甲胺2-amino-3-cyano-4-chloroquinoline乙醇 作用下, 以 为溶剂, 反应 3.0h, 以to obtain 5.2 g of title compound, mp.: 208° C.的产率得到2-amino-3-cyano-4-thenylaminoquinoline
    参考文献:
    名称:
    Aminoquinoline and aminopyridine derivatives and their use as adenosine a3 ligands
    摘要:
    通式(I)的化合物,其中R4和R5代表氢原子或共同形成1,3-丁二烯基团,可选地被甲二氧基基团或一个或多个直链或支链C1-4烷基团,直链或支链C1-4烷氧基团,羟基或卤素原子取代;是强的腺苷A3受体配体,优选地为拮抗剂。
    公开号:
    US06969723B2
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文献信息

  • Triazolo-quinolin derivatives useful as adenosine receptor ligands
    申请人:Aranyi Peter
    公开号:US20050124648A1
    公开(公告)日:2005-06-09
    The present invention relates to adenosine A- 3? receptor ligands of the general formula (I), within those preferably antagonists, as well as their salts, solvates and isomers, and the pharmaceutical compositions containing them, to the use of the compounds of the general formula (I), as well as their salts, solvates and isomers, to the preparation of the compounds of the general formula (I) and theirs salts, solvates and isomers, furthermore to the new intermediates of the general formulae (II) and to the preparation thereof.
    本发明涉及通式(I)的腺苷A-3受体配体,其中最好为拮抗剂,以及它们的盐、溶剂合物和异构体,以及包含它们的制药组合物,以及通式(I)化合物及其盐、溶剂合物和异构体的用途,以及制备通式(I)化合物及其盐、溶剂合物和异构体,此外还涉及通式(II)的新中间体及其制备。
  • Imidazoquinoline derivatives
    申请人:Aranyl Peter
    公开号:US20050070566A1
    公开(公告)日:2005-03-31
    The present invention relates to adenosine A 3 receptor ligands of the general formula (I), within those preferably antagonists, as well as their salts, solvates and isomers, and the pharmaceutical compositions containings them, to the use of the compounds of the general formula (I), as well as their salts, solvates and isomers, to the preparation of the compounds of the general formula (I) and (heir salts, solvates and isomers, furthermore to the new intermediates of the general formulae (II) and (III) and to the preparation thereof.
    本发明涉及通式(I)的腺苷A3受体配体,其中最好是拮抗剂,以及它们的盐、溶剂合物和异构体,以及含有它们的药物组合物,以及通式(I)化合物及其盐、溶剂合物和异构体的用途,以及制备通式(I)化合物及其盐、溶剂合物和异构体,此外还涉及通式(II)和(III)的新中间体及其制备。
  • Aminoquinoline and aminopyridine derivatives and their use as adenosine a3 ligands
    申请人:——
    公开号:US20040186133A1
    公开(公告)日:2004-09-23
    Compounds of general formula (I), wherein R 4 and R 5 stand for hydrogen atom or form together an 1,3-butadienyl group, optionally substituted by a methylenedioxy group or one or more straight or branched C 1-4 alkyl group, straight or branched C 1-4 alkoxy group, hydroxy group or halogen atom; are strong adenosine A 3 receptor ligands preferably antagonists. 1
    通式(I)的化合物,其中R4和R5代表氢原子或形成1,3-丁二烯基团,可选择性地被甲二氧基基团或一个或多个直链或支链C1-4烷基团,直链或支链C1-4烷氧基团,羟基或卤原子所取代;是强的腺苷A3受体配体,最好是拮抗剂。1
  • Triazolo-Quinolin Derivatives Useful as Adenosine Receptor Ligands
    申请人:Aranyi Peter
    公开号:US20080146604A1
    公开(公告)日:2008-06-19
    The present invention relates to adenosine A 3 receptor ligands of the general formula (I), within those preferably antagonists, as well as their salts, solvates and isomers, and the pharmaceutical compositions containing them, to the use of the compounds of the general formula (I), as well as their salts, solvates and isomers, to the preparation of the compounds of the general formula (I) and their salts, solvates and isomers, furthermore to the new intermediates of the general formulae (II) and to the preparation thereof.
    本发明涉及通式(I)的腺苷A3受体配体,其中最好是拮抗剂,以及它们的盐、溶剂化物和异构体,以及包含它们的制药组合物,还涉及通式(I)的化合物及其盐、溶剂化物和异构体的使用,以及制备通式(I)的化合物及其盐、溶剂化物和异构体,并涉及通式(II)的新中间体及其制备。
  • AMINOQUINOLINE AND AMINOPYRIDINE DERIVATIVES AND THEIR USE AS ADENOSINE A3 LIGANDS
    申请人:SANOFI
    公开号:EP1390349B1
    公开(公告)日:2012-07-25
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