[2-(3-fluoro-phenyl)-5-isopropyl-2H-pyrazol-3-yl]-carbamic acid phenyl ester | 937388-17-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: [2-(3-fluoro-phenyl)-5-isopropyl-2H-pyrazol-3-yl]-carbamic acid phenyl ester
• 英文别名: phenyl N-[2-(3-fluorophenyl)-5-propan-2-ylpyrazol-3-yl]carbamate
• CAS: 937388-17-5
• 化学式: C₁₉H₁₈FN₃O₂
• 分子量: 339.369
• InChiKey: KQPDHARUNOVBAE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  25
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  56.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-((1-methyl-1H-pyrazolo[3,4-c]pyridin-4-yl)ethynyl)-phenylamine 、 [2-(3-fluoro-phenyl)-5-isopropyl-2H-pyrazol-3-yl]-carbamic acid phenyl ester 在 吡啶 作用下， 以 四氢呋喃 为溶剂， 反应 0.25h， 生成 1-[2-(3-Fluoro-phenyl)-5-isopropyl-2H-pyrazol-3-yl]-3-[3-(1-methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenyl]-urea
  参考文献：
  名称：

  Alkynylaryl compounds and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same

  摘要：

  该发明涉及通式（I）所示的炔基芳基化合物：其中A、B、D、E、Ra、R1、R3、R4、R5和q如权利要求中所定义，并且其盐、N-氧化物、溶剂合物和前药，包括所述炔基芳基化合物的药物组合物，制备所述炔基芳基化合物的方法，用于所述方法的有用中间化合物，以及用于所述中间化合物在制备所述炔基芳基化合物时的用途，以及用于制备治疗失调血管生长疾病或伴随失调血管生长的疾病的药物组合物的所述炔基芳基化合物的用途。

  公开号：

  EP2070929A1

文献信息

• 3-H-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same.
  申请人：HARTUNG Ingo

  公开号：US20090062273A1

  公开（公告）日：2009-03-05

  The invention relates to 3-H-pyrazolopyridines according to the general formula (I): in which A, B, D, E, R a , R 1 , R 2 , R 3 , R 4 , R 5 and q are as defined in the claims, and salts, N-oxides, solvates and prodrugs thereof, to pharmaceutical compositions comprising said 3-H-pyrazolopyridine compounds, to methods of preparing said 3-H-pyrazolopyridines, to intermediate compounds useful in said methods, to uses of said intermediate compounds in the preparation of said 3-H-pyrazolopyridines, as well as to uses of said 3-H-pyrazolopyridines for manufacturing a pharmaceutical composition for the treatment of diseases of dysregulated vascular growth or of diseases which are accompanied with dysregulated vascular growth, wherein the compounds effectively interfere with Tie2 signalling.

  本发明涉及符合通式(I)的3-H-吡唑吡啶类化合物： 其中A、B、D、E、Ra、R1、R2、R3、R4、R5和q如权利要求中所定义的，并且涉及其盐、N-氧化物、溶剂合物和前药，涉及包含所述3-H-吡唑吡啶类化合物的制药组合物，制备所述3-H-吡唑吡啶类化合物的方法，有用于所述方法的中间化合物，以及有用于制备用于治疗失调血管生长的疾病或伴随失调血管生长的疾病的制药组合物的3-H-吡唑吡啶类化合物的用途，其中所述化合物有效地干扰Tie2信号传导。
• ALKYNYLARYL COMPOUNDS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME
  申请人：Hartung Ingo

  公开号：US20100261730A1

  公开（公告）日：2010-10-14

  The invention relates to alkynylaryl compounds according to the general formula (I) in which A, B, D, E, R a , R 1 , R 3 , R 4 , R 5 and q are as defined in the claims, and salts, N-oxides, solvates and prodrugs thereof, to pharmaceutical compositions comprising said alkynylaryl compounds, to methods of preparing said alkynylaryl compounds, to intermediate compounds useful in said methods, to uses of said intermediate compounds in the preparation of said alkynylaryl compounds, as well as to uses of said alkynylaryl compounds for manufacturing a pharmaceutical composition for the treatment of diseases of dysregulated vascular growth or of diseases which are accompanied with dysregulated vascular growth.

  本发明涉及通式(I)的炔基芳基化合物，其中A、B、D、E、Ra、R1、R3、R4、R5和q如权利要求所定义的，以及其盐、N-氧化物、溶剂合物和前药，包括含有该炔基芳基化合物的制药组合物，制备该炔基芳基化合物的方法，用于该方法的中间体化合物，以及用于制备治疗失调血管生长疾病或伴随失调血管生长的疾病的制药组合物的该炔基芳基化合物的用途。
• N-[4-(1-H-pyrazolo[3,4-c]pyridin-4-yl)phenyl]-N'-[(hetero)aryl]-urea compounds, pharmaceutical compositions comprising them, their preparation and their use as Tie2-kinase inhibitors
  申请人：Bayer Schering Pharma Aktiengesellschaft

  公开号：EP2042500A1

  公开（公告）日：2009-04-01

  The invention relates to 3-H-pyrazolopyridines according to the general formula (I): in which A, B, D, E, Ra, R1, R2, R3, R4, R5 and q are as defined in the claims, and salts, N-oxides, solvates and prodrugs thereof, to pharmaceutical compositions comprising said 3-H-pyrazolopyridine compounds, to methods of preparing said 3-H-pyrazolopyridines, to intermediate compounds useful in said methods, to uses of said intermediate compounds in the preparation of said 3-H-pyrazolopyridines, as well as to uses of said 3-H-pyrazolopyridines for manufacturing a pharmaceutical composition for the treatment of diseases of dysregulated vascular growth or of diseases which are accompanied with dysregulated vascular growth, wherein the compounds effectively interfere with Tie2 signalling.

  本发明涉及通式（I）的 3-H-吡唑并吡啶： 其中 A、B、D、E、Ra、R1、R2、R3、R4、R5 和 q 如权利要求书中所定义，及其盐类、N-氧化物、溶剂和原药，涉及包含所述 3-H-吡唑并吡啶化合物的药物组合物，涉及制备所述 3-H-吡唑并吡啶的方法，涉及在所述方法中有用的中间化合物、所述中间化合物在制备所述 3-H-吡唑并吡啶化合物中的用途，以及所述 3-H-吡唑并吡啶化合物在制造药物组合物中的用途，所述药物组合物用于治疗血管生长失调疾病或伴随血管生长失调的疾病，其中所述化合物可有效干扰 Tie2 信号。
• 3-H-PYRAZOLOPYRIDINES AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME
  申请人：Bayer Schering Pharma Aktiengesellschaft

  公开号：EP2125808A2

  公开（公告）日：2009-12-02
• US8481539B2
  申请人：——

  公开号：US8481539B2

  公开（公告）日：2013-07-09