N-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(4-methylpiperazin-1-yl)ethoxy]quinazolin-4-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: N-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(4-methylpiperazin-1-yl)ethoxy]quinazolin-4-amine
• 英文别名: 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(4-methylpiperazin-1-yl)ethoxy)quinazoline
• 化学式: C₂₂H₂₅ClFN₅O₂
• 分子量: 445.924
• InChiKey: GSFNVLNOUTVLFC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  31
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  62.8
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  1-(2-羟乙基)-4-甲基哌嗪 、 4-(4-氯-2-氟苯基氨基)-7-羟基-6-甲氧基喹唑啉 在 三丁基膦 、 1,1'-azodicarbonyl-dipiperidine 作用下， 以 二氯甲烷 为溶剂， 以25%的产率得到N-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(4-methylpiperazin-1-yl)ethoxy]quinazolin-4-amine
  参考文献：
  名称：

  Novel 4-Anilinoquinazolines with C-7 Basic Side Chains:  Design and Structure Activity Relationship of a Series of Potent, Orally Active, VEGF Receptor Tyrosine Kinase Inhibitors

  摘要：

  We have previously shown that 4-anilinoquinazolines can be potent inhibitors of vascular endothelial growth factor (VEGF) receptor (Flt-1 and KDR) tyrosine kinase activity. A novel subseries of 4-anilinoquinazolines that possess basic side chains at the C-7 position of the quinazoline nucleus have been synthesized. This subseries contains potent, nanomolar inhibitors of KDR (median IC50 0.02 muM, range 0.001-0.04 muM), which are comparatively less potent vs Flt-1 tyrosine kinase (median IC50 0.55 muM, range 0.02-1.6 muM). The compounds also retain some inhibitory activity against the tyrosine kinase associated to the endothelial growth factor receptor (EGFR) (median IC50 0.2 muM, range 0.075-0.8 muM) but demonstrate selectivity vs that associated to the FGF receptor 1 (median IC50 2.5 muM, range 0.9-19 muM). This selectivity profile is also evident in a growth factor-stimulated human endothelial cell (HUVEC) proliferation assay (i.e., inhibition of VEGF > EGF > FGF), with inhibition of VEGF-induced proliferation being achieved at nanomolar concentrations (median IC50 0.06 muM). Further examination of compound 2 (ZD6474) in recombinant enzyme assays revealed excellent selectivity for the inhibition of KDR tyrosine kinase (IC50 0.04 muM) vs the kinase activity of erbB2, MEK, CDK-2, Tie-2, IGFR-1R, PDK, PDGFRbeta, and AKT (IC50 range: 1.1 to >100 muM). Anilinoquinazolines possessing basic C-7 side chains exhibited markedly improved aqueous solubility over previously described anilinoquinazolines possessing neutral C-7 side chains (up to 500-fold improvement at pH 7.4). In addition, aqueous solubility of the neutral fraction present at pH 7.4 of the basic subseries of anilinoquinazoline proved to be higher than that of the neutral analogue 1 (ZD4190). Oral administration of representative compounds to mice (50 mg/kg) produced plasma levels between 0.2 and 3 muM at 24 h after dosing. Our development candidate 2 demonstrated a very attractive in vitro profile combined with excellent solubility (330 muM at pH 7.4) and good oral bioavailability in rat and dog (>80 and >50%, respectively). This compound demonstrated highly significant, dose-dependent, antitumor activity in athymic mice. Once daily oral administration of 100 mg/kg of compound 2 for 21 days inhibited the growth of established Calu-6 lung carcinoma xenografts by 79% (P < 0.001, Mann Whitney rank sum test), and substantial inhibition (36%, P < 0.02) was evident with 12.5 mg/kg/day.

  DOI：

  10.1021/jm011022e

文献信息

• 4-anilinoquinazoline derivatives
  申请人：Zeneca Limited

  公开号：US06291455B1

  公开（公告）日：2001-09-18

  The invention relates to quinazoline derivatives of formula (I) (wherein: R1 represents hydrogen or methoxy; R2 represents methoxy, ethoxy, 2-methoxyethoxy, 3-methoxypropoxy, 2-ethoxyethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 2-hydroxyethoxy, 3-hydroxypropoxy, 2-(N,N-dimethylamino)ethoxy, 3-(N,N-dimethylamino)propoxy, 2-morpholinoethoxy, 3-morpholinopropoxy, 4-morpholinobutoxy, 2-piperidinoethoxy, 3-piperidinopropoxy, 4-piperidinobutoxy, 2-(piperazin-1-yl)ethoxy, 3-(piperazin-1-yl)propoxy, 4-(piperazin-1-yl)butoxy, 2-(4-methylpiperazin-1-yl)ethoxy, 3-(4methylpiperazin-1-yl)propoxy or 4-(4-methylpiperazin-1-yl)butoxy; the phenyl group bearing (R3)2 is selected from: 2-fluoro-5-hydroxyphenyl, 4-bromo-2-fluorophenyl, 2,4-difluorophenyl, 4-chloro-2-fluorophenyl, 2-fluoro-4-methylphenyl, 2-fluoro-4-methoxyphenyl, 4-bromo-3-hydroxyphenyl, 4-fluoro-3-hydroxyphenyl, 4-chloro-3-hydroxyphenyl, 3-hydroxy-4-methylphenyl, 3-hydroxy-4-methoxyphenyl and 4-cyano-2-fluorophenyl); and salts thereof, processes for their preparation and pharmaceutical compositions containing a compound of formula (I) or a pharmaceutically acceptable salt thereof as active ingredient The compounds of formula (I) and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis

  本发明涉及公式（I）的喹唑啉衍生物（其中：R1代表氢或甲氧基；R2代表甲氧基、乙氧基、2-甲氧基乙氧基、3-甲氧基丙氧基、2-乙氧基乙氧基、三氟甲氧基、2,2,2-三氟乙氧基、2-羟基乙氧基、3-羟基丙氧基、2-(N,N-二甲基氨基)乙氧基、3-(N,N-二甲基氨基)丙氧基、2-吗啉基乙氧基、3-吗啉基丙氧基、4-吗啉基丁氧基、2-哌啶基乙氧基、3-哌啶基丙氧基、4-哌啶基丁氧基、2-(哌嗪-1-基)乙氧基、3-(哌嗪-1-基)丙氧基、4-(哌嗪-1-基)丁氧基、2-(4-甲基哌嗪-1-基)乙氧基、3-(4-甲基哌嗪-1-基)丙氧基或4-(4-甲基哌嗪-1-基)丁氧基；带有（R3）2的苯基被选择自：2-氟-5-羟基苯基、4-溴-2-氟苯基、2,4-二氟苯基、4-氯-2-氟苯基、2-氟-4-甲基苯基、2-氟-4-甲氧基苯基、4-溴-3-羟基苯基、4-氟-3-羟基苯基、4-氯-3-羟基苯基、3-羟基-4-甲基苯基、3-羟基-4-甲氧基苯基和4-氰基-2-氟苯基）及其盐，以及制备它们的方法和含有公式（I）的化合物或其药学上可接受的盐作为活性成分的制药组合物。公式（I）的化合物及其药学上可接受的盐抑制VEGF的作用，这是治疗包括癌症和类风湿性关节炎在内的多种疾病状态的有价值特性。
• 4-ANILINOQUINAZOLINE DERIVATIVES
  申请人：AstraZeneca AB

  公开号：EP0885198B1

  公开（公告）日：2001-12-19
• US6291455B1
  申请人：——

  公开号：US6291455B1

  公开（公告）日：2001-09-18
• [EN] 4-ANILINOQUINAZOLINE DERIVATIVES<br/>[FR] DERIVES DE 4-ANILINOQUINAZOLINE
  申请人：ZENECA LIMITED

  公开号：WO1997032856A1

  公开（公告）日：1997-09-12

  (EN) The invention relates to quinazoline derivatives of formula (I) (wherein: R1 represents hydrogen or methoxy; R2 represents methoxy, ethoxy, 2-methoxyethoxy, 3-methoxypropoxy, 2-ethoxyethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 2-hydroxyethoxy, 3-hydroxypropoxy, 2-(N,N-dimethylamino)ethoxy, 3-(N,N-dimethylamino)propoxy, 2-morpholinoethoxy, 3-morpholinopropoxy, 4-morpholinobutoxy, 2-piperidinoethoxy, 3-piperidinopropoxy, 4-piperidinobutoxy, 2-(piperazin-1-yl)ethoxy, 3-(piperazin-1-yl)propoxy, 4-(piperazin-1-yl)butoxy, 2-(4-methylpiperazin-1-yl)ethoxy, 3-(4-methylpiperazin-1-yl)propoxy or 4-(4-methylpiperazin-1-yl)butoxy; the phenyl group bearing (R3)2 is selected from: 2-fluoro-5-hydroxyphenyl, 4-bromo-2-fluorophenyl, 2,4-difluorophenyl, 4-chloro-2-fluorophenyl, 2-fluoro-4-methylphenyl, 2-fluoro-4-methoxyphenyl, 4-bromo-3-hydroxyphenyl, 4-fluoro-3-hydroxyphenyl, 4-chloro-3-hydroxyphenyl, 3-hydroxy-4-methylphenyl, 3-hydroxy-4-methoxyphenyl and 4-cyano-2-fluorophenyl); and salts thereof, processes for their preparation and pharmaceutical compositions containing a compound of formula (I) or a pharmaceutically acceptable salt thereof as active ingredient. The compounds of formula (I) and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.(FR) La présente invention, qui concerne des dérivés de quinazoline représentés par la formule générale (I) et certains de leurs sels, concerne également des procédés de préparations correspondant et des compositions pharmaceutiques contenant le composé représenté par la formule générale (I) ou certains de leurs sels galéniques servant de principe actif. Dans cette formule générale (I), R1 représente l'hydrogène ou un groupe méthoxy. R2 représente un groupe méthoxy, éthoxy, 2-méthoxyéthoxy, 3-méthoxypropoxy, 2-éthoxyéthoxy, trifluorométhoxy, 2,2,2-trifluoroéthoxy, 2-hydroxyéthoxy, 3-hydroxypropoxy, 2-(N,N-diméthylamino)éthoxy, 3-(N,N-diméthylamino)propoxy, 2-morpholinoéthoxy, 3-morpholinopropoxy, 4-morpholinobutoxy, 2-pipéridinoéthoxy, 3-pipéridinopropoxy, 4-pipéridinobutoxy, 2-(pipérazin-1-yl)éthoxy, 3-(pipérazine-1-yl)propoxy, 4-(pipérazin-1-yl)butoxy, 2-(4-méthylpipérazin-1-yl)éthoxy, 3-(4-méthylpipérazin-1-yl)propoxy ou 4-(4-méthylpipérazin-1-yl)butoxy. Le groupe phényl portant le radical (R3)2 appartient à l'ensemble des 2-fluoro-5-hydroxyphényl, 4-bromo-2-fluorophényl, 2,4-difluorophényl, 4-chloro-2-fluorophényl, 2-fluoro-4-méthylphényl, 2-fluoro-4-méthoxyphényl, 4-bromo-3-hydroxyphényl, 4-fluoro-3-hydroxyphényl, 4-chloro-3-hydroxyphényl, 3-hydroxy-4-méthylphényl, 3-hydroxy-4-méthoxyphényl et 4-cyano-2-fluorophényl. Les composés représentés par la formule générale (I) et leurs sels galéniques sont des inhibiteurs des effets du facteur VEVF (facteur de croissance de l'endothélium vasculaire), propriété intéressante pour des thérapies concernant un certain nombre de pathologies et notamment le cancer et la polyarthrite rhumatoïde.
• Novel 4-Anilinoquinazolines with C-7 Basic Side Chains:  Design and Structure Activity Relationship of a Series of Potent, Orally Active, VEGF Receptor Tyrosine Kinase Inhibitors
  作者：Laurent F. Hennequin、Elaine S. E. Stokes、Andrew P. Thomas、Craig Johnstone、Patrick A. Plé、Donald J. Ogilvie、Michael Dukes、Stephen R. Wedge、Jane Kendrew、Jon O. Curwen

  DOI：10.1021/jm011022e

  日期：2002.3.1

  We have previously shown that 4-anilinoquinazolines can be potent inhibitors of vascular endothelial growth factor (VEGF) receptor (Flt-1 and KDR) tyrosine kinase activity. A novel subseries of 4-anilinoquinazolines that possess basic side chains at the C-7 position of the quinazoline nucleus have been synthesized. This subseries contains potent, nanomolar inhibitors of KDR (median IC50 0.02 muM, range 0.001-0.04 muM), which are comparatively less potent vs Flt-1 tyrosine kinase (median IC50 0.55 muM, range 0.02-1.6 muM). The compounds also retain some inhibitory activity against the tyrosine kinase associated to the endothelial growth factor receptor (EGFR) (median IC50 0.2 muM, range 0.075-0.8 muM) but demonstrate selectivity vs that associated to the FGF receptor 1 (median IC50 2.5 muM, range 0.9-19 muM). This selectivity profile is also evident in a growth factor-stimulated human endothelial cell (HUVEC) proliferation assay (i.e., inhibition of VEGF > EGF > FGF), with inhibition of VEGF-induced proliferation being achieved at nanomolar concentrations (median IC50 0.06 muM). Further examination of compound 2 (ZD6474) in recombinant enzyme assays revealed excellent selectivity for the inhibition of KDR tyrosine kinase (IC50 0.04 muM) vs the kinase activity of erbB2, MEK, CDK-2, Tie-2, IGFR-1R, PDK, PDGFRbeta, and AKT (IC50 range: 1.1 to >100 muM). Anilinoquinazolines possessing basic C-7 side chains exhibited markedly improved aqueous solubility over previously described anilinoquinazolines possessing neutral C-7 side chains (up to 500-fold improvement at pH 7.4). In addition, aqueous solubility of the neutral fraction present at pH 7.4 of the basic subseries of anilinoquinazoline proved to be higher than that of the neutral analogue 1 (ZD4190). Oral administration of representative compounds to mice (50 mg/kg) produced plasma levels between 0.2 and 3 muM at 24 h after dosing. Our development candidate 2 demonstrated a very attractive in vitro profile combined with excellent solubility (330 muM at pH 7.4) and good oral bioavailability in rat and dog (>80 and >50%, respectively). This compound demonstrated highly significant, dose-dependent, antitumor activity in athymic mice. Once daily oral administration of 100 mg/kg of compound 2 for 21 days inhibited the growth of established Calu-6 lung carcinoma xenografts by 79% (P < 0.001, Mann Whitney rank sum test), and substantial inhibition (36%, P < 0.02) was evident with 12.5 mg/kg/day.