4-(3-{2-[4-(4-fluorobenzyl)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl]-2-oxoethyl}-2-oxoimidazolidin-1-yl)benzonitrile | 1430101-37-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: 4-(3-{2-[4-(4-fluorobenzyl)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl]-2-oxoethyl}-2-oxoimidazolidin-1-yl)benzonitrile
• 英文别名: 4-[3-[2-[4-[(4-fluorophenyl)methyl]-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl]-2-oxoethyl]-2-oxoimidazolidin-1-yl]benzonitrile
• CAS: 1430101-37-3
• 化学式: C₂₆H₂₃FN₆O₂
• 分子量: 470.506
• InChiKey: BFCSWPWBXFZMAA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  35
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  93.4
• 氢给体数：
  0
• 氢受体数：
  6

文献信息

• [EN] PYRIMIDINE AND PYRIDINE DERIVATIVES USEFUL IN THERAPY<br/>[FR] DÉRIVÉS DE PYRIMIDINE ET DE PYRIDINE UTILES EN THÉRAPIE
  申请人：PFIZER

  公开号：WO2013054185A1

  公开（公告）日：2013-04-18

  The invention provides compounds of formula (I), wherein one of X, Y and Z represents N and the other two represent CH, or X=Y-Z represents N=CH-N; W represents a CI-6 alkylene group which may be straight or branched; R1 represents H, phenyl, naphthyl, heteroaryl1, heterocyclyl1 or C3-6 cycloalkyl; wherein each phenyl, naphthyl, heteroaryl', heterocyclyl1 and C3-6 cycloalkyl group is optionally substituted, and wherein each phenyl, naphthyl, heteroaryl1, heterocyclyl1 and C3-6 cycloalkyl group is optionally fused to a 5- or 6-membered heteroaromatic or heterocyclic ring containing from 1 to 3 heteroatoms (selected from N, O and S); and each heteroaryl1, heterocyclyl1 and C3-6 cycloalkyl group is optionally fused to a benzene ring; m is 1 or 2; n is 0, 1 or 2; A is C=O or SO2; V represents a bond or C1-8 alkylene which may be straight or branched; R2 represents H, -S-(C1-6 alkyl), -SO2N(C1-6 alkyl)2, -CO2-(C1-6 alkyl), - NHCOCH2-phenyl, -OCH2- phenyl, -S02-phenyl, -NR3R4, phenyl, naphthyl, heteroaryl2, heterocyclyl2, -CO-heterocyclyl2 or C3-6 cycloalkyl; wherein each phenyl, naphthyl, heteroaryl2, heterocyclyl2 and C3-6 cycloalkyl group is optionally substituted, and wherein each phenyl, naphthyl, heteroaryl2, heterocyclyl2 and C3-6 cycloalkyl group is optionally fused to a 5- or 6-membered heteroaromatic or heterocyclic ring containing from 1 to 3 heteroatoms (selected from N, O and S); and wherein each heteroaryl2, heterocyclyl2 and C3-6 cycloalkyl group is optionally fused to a benzene ring; and pharmaceutically acceptable salts and solvates thereof. The compounds are useful as pharmaceuticals, particularly in the treatment of fibrotic diseases, cancer and pain.

  该发明提供了化合物的结构式（I），其中X、Y和Z中的一个代表N，另外两个代表CH，或者X=Y-Z代表N=CH-N；W代表可以是直链或支链的CI-6烷基基团；R1代表H、苯基、萘基、杂环芳基1、杂环基1或C3-6环烷基；其中每个苯基、萘基、杂环芳基1、杂环基1和C3-6环烷基基团可选择性地被取代，并且每个苯基、萘基、杂环芳基1、杂环基1和C3-6环烷基基团可选择性地与含有1至3个杂原子（选自N、O和S）的5-或6-成员杂芳香或杂环状环融合；每个杂环芳基1、杂环基1和C3-6环烷基基团可选择性地与苯环融合；m为1或2；n为0、1或2；A为C=O或SO2；V代表可以是直链或支链的键或C1-8烷基基团；R2代表H、-S-(C1-6烷基)、-SO2N(C1-6烷基)2、-CO2-(C1-6烷基)、-NHCOCH2-苯基、-OCH2-苯基、-S02-苯基、-NR3R4、苯基、萘基、杂环芳基2、杂环基2、-CO-杂环基2或C3-6环烷基；其中每个苯基、萘基、杂环芳基2、杂环基2和C3-6环烷基基团可选择性地被取代，并且每个苯基、萘基、杂环芳基2、杂环基2和C3-6环烷基基团可选择性地与含有1至3个杂原子（选自N、O和S）的5-或6-成员杂芳香或杂环状环融合；每个杂环芳基2、杂环基2和C3-6环烷基基团可选择性地与苯环融合；以及其在药学上可接受的盐和溶剂化合物。这些化合物在药物学上具有用途，特别是在治疗纤维化疾病、癌症和疼痛方面。