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N-[1,1,4,4-tetramethyl-1,2,3,4-tetrahydro-naphth-6-yl]-2-chloro-nicotinamide | 1135493-23-0

中文名称
——
中文别名
——
英文名称
N-[1,1,4,4-tetramethyl-1,2,3,4-tetrahydro-naphth-6-yl]-2-chloro-nicotinamide
英文别名
2-chloro-N-(5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)pyridine-3-carboxamide
N-[1,1,4,4-tetramethyl-1,2,3,4-tetrahydro-naphth-6-yl]-2-chloro-nicotinamide化学式
CAS
1135493-23-0
化学式
C20H23ClN2O
mdl
——
分子量
342.868
InChiKey
HYZLQYWXBDWOGS-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):
    5.8
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    42
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] SUBSTITUTED ARYL-AMINE DERIVATIVES AND METHODS OF USE<br/>[FR] DÉRIVÉS AMINÉS À SUBSTITUTION ARYLE ET PROCÉDÉS D'UTILISATION
    申请人:AMGEN INC
    公开号:WO2006012374A1
    公开(公告)日:2006-02-02
    The present invention provides classes of compounds, including-their pharmaceutically acceptable derivatives, useful for treating angiogenesis and related diseases such as cancer. Formula I and II wherein R is a 9- or 10-membered heterocyclyl ring selected from 7-isoquinolinyl,..2-methyl-3-oxo-2,3-dihydroindazol-6-yl, [1,6]-naphthydrin-3-yl, [1,7]-naphthydrin-2-yl, 1-oxo-2,3-dihydrobenzofuran-4-yl, 3-oxo-2,3-dihydrobenzofuran-5-yl, dihydro-benzodioxinyl, 6-quinazolinyl, 2-amino-6-quinazolinyl, 4-methylamino-6-quinazolinyl, 2,4-diamino-6 quinazolinyl, 3-oxo-3,4-dihydro-1,4-benzoxazin-6-yl, 2,2-difluoro-l;3-benzodioxol-5-yl and 2,2,3,3 tetrafluoro-2,3-dihydro-l,4-benzodioxin-6-yl, each of which is optionally substituted with one or more substituents selected from halo, haloakyl, C1-6 alkyl, C2-8 alkenyl, C2-8 alkynyl, N-dimethylamino-C1-6-alkyl, N-dimethylamino-C1-6-alkoxy, amino, alkyl-carbonylamino, morpholino-sulfonyl, amino-sulfonyl, oxazolyl, pyrrolyl,4 morpholinyl, carboxyl, cyano, and acetyl; wherein R1 in formula I is selected from unsubstituted or substituted phenyl, 5-6 membered heteroaryl, 9-10 membered bicyclic heterocyclyl and 11-14 membered tricyclic heterocyclyl, and R1 in formula II is selected from specific bicyclic heterocycles.
    本发明提供了一类化合物,包括其药用可接受的衍生物,用于治疗血管生成和相关疾病,如癌症。其中R为从7-异喹啉基、2-甲基-3-氧代-2,3-二氢吲哚-6-基、[1,6]-啶-3-基、[1,7]-啶-2-基、1-氧代-2,3-二氢苯并呋喃-4-基、3-氧代-2,3-二氢苯并呋喃-5-基、二氢苯并二氧杂环基、6-喹唑啉基、2-基-6-喹唑啉基、4-甲基-6-喹唑啉基、2,4-二基-6-喹唑啉基、3-氧代-3,4-二氢-1,4-苯并噁嗪-6-基、2,2-二-1,3-苯并二氧杂环-5-基和2,2,3,3-四-2,3-二氢-1,4-苯并二氧杂环-6-基中选择的9-或10-成员杂环基,其中每个基可选择地被一个或多个来自卤素、卤代烷基、C1-6烷基、C2-8烯基、C2-8炔基、N-二甲氨基-C1-6-烷基、N-二甲氨基-C1-6-烷氧基、基、烷基-羰基基、吗啉磺酰基、基磺酰基、噁唑基、吡咯基、吗啉基、羧基、基和乙酰基的取代基取代;其中式I中的R1从未取代或取代的苯基、5-6成员杂芳基、9-10成员双环杂环基和11-14成员三环杂环基中选择,式II中的R1从特定的双环杂环基中选择。
  • Substituted alkylamine derivatives and methods of use
    申请人:Amgen Inc.
    公开号:US20030225106A1
    公开(公告)日:2003-12-04
    Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选定的胺对预防治疗疾病有效,如血管生成介导的疾病。本发明包括新的化合物、类似物、前药和药用可接受的盐,药物组合物和预防治疗疾病和其他疾病或状况的方法,包括癌症等。本发明还涉及制造这类化合物的过程以及在此类过程中有用的中间体。
  • Substituted amine derivatives and methods of use
    申请人:Amgen Inc.
    公开号:US20030203922A1
    公开(公告)日:2003-10-30
    Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选定的胺类化合物对于预防和治疗疾病,如血管生成介导的疾病,具有有效性。该发明涵盖了新颖的化合物、类似物、前药和其药用可接受盐,用于预防和治疗涉及癌症等疾病和其他疾患或病况的药物组合物和方法。该发明还涉及制备这些化合物的方法以及在这些方法中有用的中间体。
  • Substituted arylamine derivatives and methods of use
    申请人:——
    公开号:US20020147198A1
    公开(公告)日:2002-10-10
    Selected compounds are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对预防和治疗疾病,如介导血管生成的疾病,具有有效性。该发明涵盖了新颖的化合物、类似物、前药和其药用可接受的衍生物,用于预防和治疗涉及癌症等疾病和其他疾病或情况的药物组合物和方法。该发明还涉及用于制备这种化合物的工艺,以及在这些工艺中有用的中间体。
  • Substituted aryl-amine derivatives and methods of use
    申请人:Yuan Chenguang Chester
    公开号:US20060040966A1
    公开(公告)日:2006-02-23
    Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds of Formula I and II wherein R, R 1 and R 2 for each formula are defined herein. The invention further includes analogs, prodrugs and pharmaceutically acceptable salts and derivatives of Formulas I and II, as well as pharmaceutical compositions, medicaments and methods thereof for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选定的胺类化合物对于预防和治疗由血管生成介导的疾病等疾病有效。该发明涵盖了式I和式II的新型化合物,其中每个式中的R、R1和R2如本文所定义。该发明还包括式I和式II的类似物、前药和药物可接受的盐和衍生物,以及用于预防和治疗涉及癌症等疾病和其他疾病或病症的药物组合物、药物和方法。该发明还涉及制备这种化合物的工艺以及在这种工艺中有用的中间体。
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