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4-{2-[6-(3-amino-piopylamino)-pyrido [3,4-d] pyrimidin-4-ylamino]-phenoxy}-butyric acid | 855995-85-6

中文名称
——
中文别名
——
英文名称
4-{2-[6-(3-amino-piopylamino)-pyrido [3,4-d] pyrimidin-4-ylamino]-phenoxy}-butyric acid
英文别名
4-[2-[[6-(3-Aminopropylamino)pyrido[3,4-d]pyrimidin-4-yl]amino]phenoxy]butanoic acid
4-{2-[6-(3-amino-piopylamino)-pyrido [3,4-d] pyrimidin-4-ylamino]-phenoxy}-butyric acid化学式
CAS
855995-85-6
化学式
C20H24N6O3
mdl
——
分子量
396.449
InChiKey
PXTROIPUOPMZPD-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):
    0.2
  • 重原子数:
    29
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    135
  • 氢给体数:
    4
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    4-{2-[6-(3-amino-piopylamino)-pyrido [3,4-d] pyrimidin-4-ylamino]-phenoxy}-butyric acid 在 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下, 以 DMF (N,N-dimethyl-formamide) 为溶剂, 生成 7H, 21H-6, 4-(nitrilometheno) pyrimido [5,4-m] [1, 6,10, 15] benzoxa-triazacycloheptadecin-12 (13H)-one, 8,9, 10,11, 14,15-hexahydro-
    参考文献:
    名称:
    [EN] PYRIDO- AND PYRIMIDOPYRIMIDINE DERIVATIVES AS ANTI- PROLIFERATIVE AGENTS
    [FR] ANTI-PROLIFERANTS A BASE DE DERIVES PYRIDO- ET PYRIMIDOPYRIMIDINE
    摘要:
    本发明涉及公式(I)的化合物,其N-氧化物形式,药学上可接受的加合盐及其立体化异构形式,其中a1-a2=a3-a4代表从N-CH=CH-CH,N-CH N-CH或CH-CH=N-CH中选择的二价基团;Z代表NH;Y代表-C3-9烷基-,-Cl-5烷基-NR13-Cl-5烷基-,-C1-6烷基-NH-CO-或-CO-NH -C1-6烷基-;X1代表-O-或-NR11-;X2代表-C1-2烷基-,-O-C1-2烷基,-O-或-O-CH2-;R1代表氢或卤素;R2代表氢,氰基,卤素,羟基甲酰-Cl-4烷氧基甲酰-,Het16-羰基或Ar5;R3代表氢;R4代表羟基,C1-4烷氧基-,Ar4-C1-4烷氧基或R4代表Cl-4烷氧基,其中一个或可能两个或更多取代基选择自C1-4烷氧基-或Het2-;R11代表氢;R12代表氢,Cl-4烷基-或Cl-4烷氧基甲酰-;R13代表Het14-Cl-4烷基,特别是吗啡啶基-Cl-4烷基;Het2代表选择自吗啡啶基或哌啶基的杂环,可选地取代为C1-4烷基-,最好是甲基;Het14代表吗啡啶基;Het16代表选择自吗啡啶基或吡咯啉基的杂环;Ar4代表苯基;Ar5代表苯基,可选地取代为氰基。
    公开号:
    WO2005058913A1
  • 作为产物:
    描述:
    4-{2-[6-(3-amino-piopylamino)-pyrido [3,4-d] pyrimidin-4-ylamino]-phenoxy}-butyric acid ethyl ester 在 lithium hydroxide 作用下, 以 四氢呋喃 为溶剂, 以100%的产率得到4-{2-[6-(3-amino-piopylamino)-pyrido [3,4-d] pyrimidin-4-ylamino]-phenoxy}-butyric acid
    参考文献:
    名称:
    [EN] PYRIDO- AND PYRIMIDOPYRIMIDINE DERIVATIVES AS ANTI- PROLIFERATIVE AGENTS
    [FR] ANTI-PROLIFERANTS A BASE DE DERIVES PYRIDO- ET PYRIMIDOPYRIMIDINE
    摘要:
    本发明涉及公式(I)的化合物,其N-氧化物形式,药学上可接受的加合盐及其立体化异构形式,其中a1-a2=a3-a4代表从N-CH=CH-CH,N-CH N-CH或CH-CH=N-CH中选择的二价基团;Z代表NH;Y代表-C3-9烷基-,-Cl-5烷基-NR13-Cl-5烷基-,-C1-6烷基-NH-CO-或-CO-NH -C1-6烷基-;X1代表-O-或-NR11-;X2代表-C1-2烷基-,-O-C1-2烷基,-O-或-O-CH2-;R1代表氢或卤素;R2代表氢,氰基,卤素,羟基甲酰-Cl-4烷氧基甲酰-,Het16-羰基或Ar5;R3代表氢;R4代表羟基,C1-4烷氧基-,Ar4-C1-4烷氧基或R4代表Cl-4烷氧基,其中一个或可能两个或更多取代基选择自C1-4烷氧基-或Het2-;R11代表氢;R12代表氢,Cl-4烷基-或Cl-4烷氧基甲酰-;R13代表Het14-Cl-4烷基,特别是吗啡啶基-Cl-4烷基;Het2代表选择自吗啡啶基或哌啶基的杂环,可选地取代为C1-4烷基-,最好是甲基;Het14代表吗啡啶基;Het16代表选择自吗啡啶基或吡咯啉基的杂环;Ar4代表苯基;Ar5代表苯基,可选地取代为氰基。
    公开号:
    WO2005058913A1
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文献信息

  • PYRIDO- AND PYRIMIDOPYRIMIDINE DERIVATIVES AS ANTI-PROLIFERATIVE AGENTS
    申请人:Janssen Pharmaceutica NV
    公开号:EP1697384B1
    公开(公告)日:2008-04-02
  • Pyrido-and pyrimidopyrimidine derivatives as anti-profilerative agents
    申请人:Freyne Jean Edgard Eddy
    公开号:US20070078132A1
    公开(公告)日:2007-04-05
    The present invention concerns the compounds of formula the N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein a 1 -a 2 =a 3 -a 4 represents a divalent radical selected from N—CH═CH—CH, N—CH═N—CH or CH—CH═N—CH; Z represents NH; Y represents —C 3-9 alkyl-, —C 1-5 alkyl-NR 13 —C 1-5 alkyl-, —C 1-6 alkyl-NH—CO— or —CO—NH—C 1-6 alkyl-; X 1 represents —O— or —NR 11 —; X 2 represents —C 1-2 alkyl-, —O—C 1-2 alkyl, —O— or —O—CH 2 —; R 1 represents hydrogen or halo; R 2 represents hydrogen, cyano, halo, hydroxycarbonyl-, C 1-4 alkyloxycarbonyl-, Het 16 -carbonyl- or Ar 5 ; R 3 represents hydrogen; R 4 represents hydroxy, C 1-4 alkyloxy-, Ar 4 —C 1-4 alkyloxy or R 4 represents C 1-4 alkyloxy substituted with one or where possible two or more substituents selected from C 1-4 alkyloxy- or Het 2 -; R 11 represents hydrogen; R 12 represents hydrogen, C 1-4 alkyl- or C 1-4 alkyl-oxy-carbonyl-; R 13 represents Het 14 -C 1-4 alkyl, in particular morpholinyl-C 1-4 alkyl; Het 2 represents a heterocycle selected from morpholinyl or piperidinyl optionally substituted with C 1-4 alkyl-, preferably methyl; Het 14 represents morpholinyl; Het 16 represents a heterocycle selected from morpholinyl or pyrrolidinyl; Ar 4 represents phenyl; Ar 5 represents phenyl optionally substituted with cyano.
  • PYRIDO-AND PYRIMIDOPYRIMIDINE DERIVATIVES AS ANTI-PROLIFERATIVE AGENTS
    申请人:Freyne Eddy Jean Edgard
    公开号:US20100173913A1
    公开(公告)日:2010-07-08
    The present invention concerns the compounds of formula the N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein a 1 -a 2 =a 3 -a 4 represents a divalent radical selected from N—CH═CH—CH, N—CH═N—CH or CH—CH═N—CH; Z represents NH; Y represents —C 3-9 alkyl-, —C 1-5 alkyl-NR 13 —C 1-5 alkyl-, —C 1-6 alkyl-NH—CO— or —CO—NH—C 1-6 alkyl-; X 1 represents —O— or —NR 11 —; X 2 represents —C 1-2 alkyl-, —O—C 1-2 alkyl, —O— or —O—CH 2 —; R 1 represents hydrogen or halo; R 2 represents hydrogen, cyano, halo, hydroxycarbonyl-, C 1-4 alkyloxycarbonyl-, Het 16 -carbonyl- or Ar 5 ; R 3 represents hydrogen; R 4 represents hydroxy, C 1-4 alkyloxy-, Ar 4 —C 1-4 alkyloxy or R 4 represents C 1-4 alkyloxy substituted with one or where possible two or more substituents selected from C 1-4 alkyloxy- or Het 2 -; R 11 represents hydrogen; R 12 represents hydrogen, C 1-4 alkyl- or C 1-4 alkyl-oxy-carbonyl-; R 13 represents Het 14 -C 1-4 alkyl, in particular morpholinyl-C 1-4 alkyl; Het 2 represents a heterocycle selected from morpholinyl or piperidinyl optionally substituted with C 1-4 alkyl-, preferably methyl; Het 14 represents morpholinyl; Het 16 represents a heterocycle selected from morpholinyl or pyrrolidinyl; Ar 4 represents phenyl; Ar 5 represents phenyl optionally substituted with cyano.
  • PYRIDO- AND PYRIMIDOPYRIMIDINE DERIVATIVES AS ANTI-PROFILERATIVE AGENTS
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:US20130231353A1
    公开(公告)日:2013-09-05
    The present invention concerns the compounds of formula wherein a 1 -a 2 =a 3 -a 4 represents a divalent radical selected from N—CH═CH—CH, N—CH═N—CH or CH—CH═N—CH; Z represents NH; Y represents —C 3-9 alkyl-, —C 1-5 alkyl-NR 13 —C 1-5 alkyl-, —C 1-6 alkyl-NH—CO— or —CO—NH—C 1-6 alkyl-; X 1 represents —O— or —NR 11 —; X 2 represents —C 1-2 alkyl-, —O—C 1-2 alkyl, —O— or —O—CH 2 —; R 1 represents hydrogen or halo; R 2 represents hydrogen, cyano, halo, hydroxycarbonyl-, C 1-4 alkyloxycarbonyl-, Het 16 -carbonyl- or Ar 5 ; R 3 represents hydrogen; R 4 represents hydroxy, C 1-4 alkyloxy-, Ar 4 —C 1-4 alkyloxy or substituted C 1-4 alkyloxy; R 11 represents hydrogen; R 12 represents hydrogen, C 1-4 alkyl- or C 1-4 alkyl-oxy-carbonyl-; R 13 represents morpholinyl-C 1-4 alkyl; Het 2 represents morpholinyl or piperidinyl optionally substituted with C 1-4 alkyl-, preferably methyl; Het 14 represents morpholinyl; Het 16 represents morpholinyl or pyrrolidinyl; Ar 4 represents phenyl; Ar 5 represents phenyl optionally substituted with cyano.
  • US7799772B2
    申请人:——
    公开号:US7799772B2
    公开(公告)日:2010-09-21
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