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4-[4-benzyl-5-(4-methoxy-piperidin-1-ylmethyl)-4H-[1,2,4]triazol-3-yl]-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl

中文名称
——
中文别名
——
英文名称
4-[4-benzyl-5-(4-methoxy-piperidin-1-ylmethyl)-4H-[1,2,4]triazol-3-yl]-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl
英文别名
2-[4-[4-Benzyl-5-[(4-methoxypiperidin-1-yl)methyl]-1,2,4-triazol-3-yl]piperidin-1-yl]pyridine
4-[4-benzyl-5-(4-methoxy-piperidin-1-ylmethyl)-4H-[1,2,4]triazol-3-yl]-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl化学式
CAS
——
化学式
C26H34N6O
mdl
——
分子量
446.596
InChiKey
DKNRPLUUGUZOKC-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
  • 重原子数:
    33
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    59.3
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • [EN] TRIAZOLE COMPOUNDS FOR THE TREATMENT OF DYSMENORRHOEA<br/>[FR] COMPOSES TRIAZOLE POUR LE TRAITEMENT DE LA DYSMENORRHEE
    申请人:PFIZER LTD
    公开号:WO2004037809A1
    公开(公告)日:2004-05-06
    A compound of formula (I), a pharmaceutically acceptable salt or solvate thereof, wherein R' represents C,-C6 alkyl, -(CH2)c-[C3-C8 cycloalkyl]-, -(CH2)C -W or -(CH2)C-Z-(CH2)dW; W represents C1-C6 alkyl, C1-C6 alkyloxy, -C02[C1-C6 alkyl], -CONR4R5, an optionally substituted phenyl group, NR4R5, het2 or het3; Z represents O or S(O)g; g represents 0, 1 or 2; R2 represents a phenyl group, optionally fused to a 5- or 6- membered aryl or heterocyclic group which may contain one or more heteroatoms selected from N, O or S; the phenyl group and the optionally fused group being optionally substituted; Ring A represents a 4-, 5- or 6- membered saturated heterocyclic group containing at least one N; Ring B represents a phenyl group or het1, each group being optionally substituted; R7 independently represents H1 C1-C6 alkyl, OR3, -(CH2)e-R3 or -(CH2)f-O-(CH2)e-R3; at each occurrence R3 independently represents H1 C1-C6 alkyl optionally substituted by Y, -(CH2)g [C3-C8 cycloalkyl], phenyl, benzyl, pyridyl or pyrimidyl; at each occurrence R4 and R5 independently represent H1 Cl-C6 alkyl (optionally substituted with Cl-C6 alkyloxy), (CH2)gC02-[C1-C6 alkyl], -S02Me, -(CH2)g [C3-C8 cycloalkyl], S02Me, phenyl, benzyl, pyridyl or pyrimidyl; or R4 and R5 together with the N atom to which they are attached represent a heterocyclic group of from 3 to 8 atoms; Y independently represents a phenyl group, NR4R5 or het4, the phenyl group being optionally substituted; het1 represents a 4-, 5- or 6- membered saturated, or unsaturated, heterocyclic group containing at least one N (but which may also contain one or more O or S atoms); het2 and het4 represent an optionally substituted 4-, 5-, 6- or 7- membered saturated, or unsaturated, heterocyclic group containing at least one N (but which may 5 also contain one or more O or S atoms); het3 represents an optionally substituted 4-, 5-, 6- or 7- membered saturated, or unsaturated, heterocyclic group containing at least one O (but which may also contain one or mare N or S atoms); at each occurrence R6 independently represents H1 C1-C6 alkyl optionally substituted by Y, =(CH2)g [C3-C8 cycloalkyl], phenyl, benzyl, pyridyl or pyrimidyl; a and b independently represent 0 or 1; c,, d, a end g independently represent 0, 1, 2, 3 or 4; . f índeperldently represents 1, 2, 3 or 4; provided that: (i) a + b cannot equal 0; and províded,that,when R1 represents -(CH2)c-Z-(CH2)d-W and W represents.NR4R5 or any N linked heterocyclic, group then d must not be, 0 or 1; and (iii), provided that when R2 represents a phenyl group substituted by a group of, formula -(CH2)eOR3, -(CH2)e-OCOR3 or -(CH2)e,OCOR3 ;or het1,and/or het2 are substituted by a group of formula -(CH2)eOR3, (CH2),-CO2R3 or -(CH2)eOCOR3; or when R7 represents -OR3 or -(CH2)f-0-(CH2)e-R3 and e is 0; or when W represents a phenyl group substituted with -OR
    式(I)的化合物,其药学上可接受的盐或溶剂,其中R'代表C1-C6烷基,-(CH2)c-[C3-C8环烷基]-,-( )C-W或-( )C-Z-( )dW;W代表C1-C6烷基,C1-C6烷基,-C02[C1-C6烷基],-CONR4R5,一个可选择取代的基,NR4R5,het2或het3;Z代表O或S(O)g;g代表0、1或2;R2代表一个基,可选择与含有一个或多个异原子N、O或S的5-或6-成员芳基或杂环基融合;基和可选择融合的基团可选择取代;环A代表至少含有一个N的4-、5-或6-成员饱和杂环基;环B代表一个基或het1,每个基团可选择取代;R7独立地代表H1 C1-C6烷基,OR3,-( )e-R3或-( )f-O-( )e-R3;在每次出现时,R3独立地代表H1 C1-C6烷基,可选择由Y取代,-( )g[C3-C8环烷基],基,苄基吡啶基或嘧啶基;在每次出现时,R4和R5独立地代表H1 Cl-C6烷基(可选择用Cl-C6烷基取代),( )gC02-[C1-C6烷基],-S02Me,-( )g[C3-C8环烷基],S02Me,基,苄基吡啶基或嘧啶基;或R4和R5与它们连接的N原子一起代表3到8个原子的杂环基;Y独立地代表一个基,NR4R5或het4,基可选择取代;het1代表至少含有一个N的4-、5-或6-成员饱和或不饱和杂环基(但也可能含有一个或多个O或S原子);het2和het4代表一个可选择取代的4-、5-、6-或7-成员饱和或不饱和杂环基,至少含有一个N(但也可能含有一个或多个O或S原子);het3代表一个可选择取代的4-、5-、6-或7-成员饱和或不饱和杂环基,至少含有一个O(但也可能含有一个或多个N或S原子);在每次出现时,R6独立地代表H1 C1-C6烷基,可选择由Y取代,=( )g[C3-C8环烷基],基,苄基吡啶基或嘧啶基;a和b独立地代表0或1;c、d、a和g独立地代表0、1、2、3或4;f独立地代表1、2、3或4;条件是:(i) a+b不能等于0;并且,条件是,当R1代表-( )c-Z-( )d-W且W代表NR4R5或任何N连接的杂环基时,d不能为0或1;以及(iii),条件是,当R2代表一个基,被-( )eOR3,-( )e-OCOR3或-( )e-OCOR3取代;或het1和/或het2被-( )eOR3,( )e-CO2R3或-( )eOCOR3取代;或当R7代表-OR3或-( )f-O-( )e-R3且e为0时;或当W代表一个被-OR取代的基时。
  • Compounds Useful In Therapy
    申请人:Gibson Karl Richard
    公开号:US20080096950A1
    公开(公告)日:2008-04-24
    Compounds of Formula (I): and pharmaceutically acceptable salts, solvates (including hydrates) of said compounds and salts, or prodrugs of said compound, or pharmaceutically acceptable salts or solvates of said prodrugs, wherein the substituents are as herein defined, are useful in therapy, for example they may be useful for treating progesterone-mediated conditions such as endometriosis, uterine fibroids (leiomyomata), menorrhagia, adenomyosis, primary and secondary dysmenorrhoea (including symptoms of dyspareunia, dyschexia and chronic pelvic pain), or chronic pelvic pain syndrome.
    化合物的化学式(I): 以及所述化合物及其盐、溶剂化合物(包括合物)和盐、或所述化合物的前药,或所述前药的药学上可接受的盐或溶剂化合物,其中取代基如本文所定义,可用于治疗,例如它们可能对治疗孕激素介导的疾病如子宫内膜异位症、子宫肌瘤(平滑肌瘤)、月经过多、子宫腺肌病、原发性和继发性痛经(包括性交疼痛、排便疼痛和慢性盆腔疼痛症状)或慢性盆腔疼痛综合症等方面具有用处。
  • Compounds useful in therapy
    申请人:Bradley Anthony Paul
    公开号:US20070105909A1
    公开(公告)日:2007-05-10
    Compounds of formula (I), or a pharmaceutically acceptable derivative thereof, wherein R 1 and R 3 independently represent H, C 1-6 alkyl, C 3-8 cycloalkyl, or halogen; R 2 represents C 1-6 alkyl, CF 3 or aryl; a represents 1 or 2; R 4 , R 5 , R 7 and R 8 independently represent H, C 1-6 alkyl, C 1-6 alkyloxy, CN or halogen, or R 4 and R 5 , or R 7 and R 8 , together with the ring to which they are attached form an aryl or heterocyclic fused ring system; X represents C or N; Y represents CH 2 or O; R 6 represents H, CN or halo provided that, when X represents N, R 6 is absent. The compounds are useful for treating endometriosis, uterine fibroids (leiomyomata), menorrhagia, adenomyosis, primary and secondary dysmenorrhoea (including symptoms of dyspareunia, dyschexia and chronic pelvic pain), or chronic pelvic pain syndrome.
    式(I)的化合物,或其药学上可接受的衍生物,其中R1和R3独立地代表H、C1-6烷基、C3-8环烷基或卤素;R2代表C1-6烷基、CF3或芳基;a代表1或2;R4、R5、R7和R8独立地代表H、C1-6烷基、C1-6烷基、CN或卤素,或R4和R5,或R7和R8,与它们连接的环一起形成芳基或杂环融合环系统;X代表C或N;Y代表CH2或O;R6代表H、CN或卤素,但当X代表N时,R6不存在。这些化合物可用于治疗子宫内膜异位症、子宫肌瘤(平滑肌瘤)、月经过多、子宫腺肌病、原发性和继发性痛经(包括性交疼痛、性交困难和慢性盆腔疼痛症状)或慢性盆腔疼痛综合征。
  • Pyrrolidines
    申请人:Dack Kevin N.
    公开号:US20100120793A1
    公开(公告)日:2010-05-13
    This invention relates to a class of pyrrolidine compounds of formula (I), and pharmaceutically acceptable derivatives thereof, to their use in medicine, to compositions containing them, and to processes for their preparation. It also relates to intermediates used in the preparation of such compounds and derivatives. In particular the compounds of formula (I) are useful for the treatment of EP2-mediated conditions, such as endometriosis, uterine fibroids (leiomyomata), menorrhagia, adenomyosis, primary and secondary dysmenorrhoea (including symptoms of dyspareunia, dyschexia and chronic pelvic pain), chronic pelvic pain syndrome.
    这项发明涉及一类式(I)的吡咯烷化合物及其药学上可接受的衍生物,它们在医学上的应用,含有它们的组合物,以及它们的制备方法。它还涉及用于制备这类化合物和衍生物中间体。特别是式(I)的化合物对于治疗EP2介导的疾病非常有用,如子宫内膜异位症、子宫肌瘤(平滑肌瘤)、月经过多、子宫腺肌病、原发性和继发性痛经(包括性交疼痛、排便疼痛和慢性盆腔疼痛症状)、慢性盆腔疼痛综合征。
  • Azetidines
    申请人:Dack Kevin Neil
    公开号:US20080280877A1
    公开(公告)日:2008-11-13
    The invention relates to EP2 antagonist azetidines of formula (I) wherein Ar, R 1 , X, and Z are as defined herein, to their use in medicine, particularly in the treatment of endometriosis and/or uterine fibroids, to intermediates useful in their synthesis, and to compositions containing them.
    这项发明涉及到式(I)的EP2拮抗剂环丁烷,其中Ar、R1、X和Z如本文所定义,其在医学上的应用,特别是在子宫内膜异位症和/或子宫肌瘤的治疗中的应用,以及其合成中有用的中间体,以及含有它们的组合物。
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