[amino]pyrazolo[1,5-a]pyrimidine | 1159982-76-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡唑并嘧啶类
• 英文名称: [amino]pyrazolo[1,5-a]pyrimidine
• 英文别名: Pyrazolo[1,5-a]pyrimidin-2-amine
• CAS: 1159982-76-9
• 化学式: C₆H₆N₄
• mdl: MFCD11215401
• 分子量: 134.14
• InChiKey: KBFZCYFAUHHOHW-UHFFFAOYSA-N

物化性质

• 密度：
  1.50±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  56.2
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• [EN] MACROCYCLIC COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS MACROCYCLIQUES ET UTILISATIONS DE CES COMPOSÉS
  申请人：TP THERAPEUTICS INC

  公开号：WO2019023417A1

  公开（公告）日：2019-01-31

  The present disclosure relates to certain macrocyclic compounds that inhibit SRC and MET, and/or CSF1R, pharmaceutical compositions containing such compounds, and methods of using such compounds to treat cancer.

  本公开涉及抑制SRC和MET，和/或CSF1R的特定大环化合物，含有这些化合物的药物组合物，以及使用这些化合物治疗癌症的方法。
• [EN] PYRAZOLOPYRIMIDINE COMPOUNDS AND THEIR USE IN MEDICINE<br/>[FR] COMPOSES PYRAZOLOPYRIMIDINES ET LEUR UTILISATION EN MEDECINE
  申请人：VERNALIS CAMBRIDGE LTD

  公开号：WO2004087707A1

  公开（公告）日：2004-10-14

  Compounds of formula (I) or salts, N-oxides, hydrates or solvates thereof are inhibitors of kinase activity, and useful for the treatment of, for example, cancer, psoriasis or restenosis: wherein ring A is an optionally substituted carbocyclic or heterocyclic radical. Alk represents an optionally substituted divalent Cl-C6 alkylene radical. n is 0 or 1. Q represents a radical of formula -(Alk1)P (X)r-(Alk2)S -Z wherein in any compatible combination Z is hydrogen or an optionally substituted carbocyclic or heterocyclic ring; Alk1 and Alk2 are optionally substituted divalent C1-C6 alkylene radicals which may contain a -0-, -S- or -NR A_ link, wherein RA is hydrogen or Cl-C6 alkyl; X represents -0-, -S-, -(C=O)-, -(C=S)-, -SO2-, -SO-, -C(=O)O-, -OC(=O)-, -C(=O)NRA-, -NR AC(=O)-, -C(=S)NRA-, -NR AC(=S)-, - SO2NRA-, -NR ASO2-, -OC(=O)NRA-, -NR AC(=O)O-, or -NRA- wherein RA is hydrogen or C1-C6 alkyl. p, r and s are independently 0 or 1. R1 represents a radical -(Alk3)a-(Y)b-(Alk4)d-B wherein a, b and d are independently 0 or 1; Alk3 and Alk4 are optionally substituted divalent C,-C3 alkylene radicals; Y represents a monocyclic divalent carbocyclic or heterocyclic radical having from 5 to 8 ring atoms, -0-, -S-, or -NRA- wherein RA is hydrogen or C1-C6 alkyl; B represents hydrogen or halo, or an optionally substituted monocyclic carbocyclic or heterocyclic ring having from 5 to 8 ring atoms, or in the case where Y is -NRA- and b is 1, then RA and the radical -(Alk4)d-B taken together with the nitrogen to which they are attached may form an optionally substituted heterocyclic ring. R represents hydrogen, halo, Cl-C6 alkyl, Cl-C6 alkoxy, C1-C6 alkylthio, phenyl, benzyl, cycloalkyl with 3 to 6 ring atoms, or a monocyclic heterocyclic group having 5 or 6 ring atoms.

  式(I)的化合物或其盐、N-氧化物、水合物或溶剂合物是激酶活性的抑制剂，可用于治疗癌症、银屑病或再狭窄等疾病：其中环A是一个可选择取代的碳环或杂环基团。Alk代表一个可选择取代的二价Cl-C6烷基基团。n为0或1。Q代表一个公式-(Alk1)P (X)r-(Alk2)S -Z的基团，其中在任何兼容的组合中，Z为氢或一个可选择取代的碳环或杂环环；Alk1和Alk2为可选择取代的二价C1-C6烷基基团，可能包含一个-0-、-S-或-NR A_链，其中RA为氢或Cl-C6烷基；X代表-0-、-S-、-(C=O)-、-(C=S)-、-SO2-、-SO-、-C(=O)O-、-OC(=O)-、-C(=O)NRA-、-NR AC(=O)-、-C(=S)NRA-、-NR AC(=S)-、-SO2NRA-、-NR ASO2-、-OC(=O)NRA-、-NR AC(=O)O-或-NRA-，其中RA为氢或C1-C6烷基。p、r和s独立地为0或1。R1代表一个基团-(Alk3)a-(Y)b-(Alk4)d-B，其中a、b和d独立地为0或1；Alk3和Alk4为可选择取代的二价C,-C3烷基基团；Y代表具有5至8个环原子的单环二价碳环或杂环基团，-0-、-S-或-NRA-，其中RA为氢或C1-C6烷基；B代表氢或卤素，或具有5至8个环原子的可选择取代的单环碳环或杂环环，或在Y为-NRA-且b为1的情况下，则RA和基团-(Alk4)d-B与它们连接的氮一起可能形成一个可选择取代的杂环环。R代表氢、卤素、Cl-C6烷基、Cl-C6烷氧基、C1-C6烷基硫基、苯基、苄基、具有3至6个环原子的环烷基，或具有5或6个环原子的单环杂环基团。
• Pyrazolopyrimidine compounds and their use in medicine
  申请人：Parratt Martin

  公开号：US20070179161A1

  公开（公告）日：2007-08-02

  Compounds of formula (I) or salts, N-oxides, hydrates or solvates thereof are inhibitors of kinase activity, and useful for the treatment of, for example, cancer, psoriasis or restenosis: wherein ring A is an optionally substituted carbocyclic or heterocyclic radical. Alk represents an optionally substituted divalent C1-C 6 alkylene radical. n is 0 or 1. Q represents a radical of formula -(Alk 1 ) p (X) r -(Alk 2 ) s -Z wherein in any compatible combination Z is hydrogen or an optionally substituted carbocyclic or heterocyclic ring; Alk 1 and Alk 2 are optionally substituted divalent C 1 -C 6 alkylene radicals which may contain a —O—, —S— or —NR A — link, wherein R A is hydrogen or C 1 -C 6 alkyl; X represents —O—, —S—, —(C═O)—, —(C═S)—, —SO 2 —, —SO—, —C(═O)O—, —OC(═O)—, —C(═O)NR A—, —NR A C(═O)—, —C(═S)NR A , —NR A C(═S)—, —SO 2 NR A —, —NR A SO 2 —, —OC(═O)NR A—, —NR A C(═O)O—, or —NR A — wherein R A is hydrogen or C 1 -C 6 alkyl. p, r and s are independently 0 or 1. R 1 represents a radical -(Alk 3 ) a -(Y)b-(Alk 4 ) d -B wherein a, b and d are independently 0 or 1; Alk 3 and Alk 4 are optionally substituted divalent C,-C3 alkylene radicals; Y represents a monocyclic divalent carbocyclic or heterocyclic radical having from 5 to 8 ring atoms, —O—, —S—, or —NR A — wherein R A is hydrogen or C 1 -C 6 alkyl; B represents hydrogen or halo, or an optionally substituted monocyclic carbocyclic or heterocyclic ring having from 5 to 8 ring atoms, or in the case where Y is —NR A — and b is 1, then R A and the radical -(Alk 4 ) d -B taken together with the nitrogen to which they are attached may form an optionally substituted heterocyclic ring. R represents hydrogen, halo, C 1 -C 6 alkyl, C1-C 6 alkoxy, C 1 -C 6 alkylthio, phenyl, benzyl, cycloalkyl with 3 to 6 ring atoms, or a monocyclic heterocyclic group having 5 or 6 ring atoms.

  式(I)化合物或其盐、N-氧化物、水合物或溶剂合物是激酶活性的抑制剂，可用于治疗癌症、牛皮癣或再狭窄等疾病：其中环A是可选取代的碳环或杂环基。Alk表示可选取代的二价C1-C6烷基基团。n为0或1。Q表示式-(Alk1)p(X)r-(Alk2)s-Z的基团，其中Z在任何兼容的组合中为氢或可选取代的碳环或杂环环；Alk1和Alk2是可选取代的二价C1-C6烷基基团，可包含—O—、—S—或—NRA—链，其中RA为氢或C1-C6烷基；X表示—O—、—S—、—(C═O)—、—(C═S)—、—SO2—、—SO—、—C(═O)O—、—OC(═O)—、—C(═O)NRA—、—NRAC(═O)—、—C(═S)NRA、—NRAC(═S)—、—SO2NRA—、—NRASO2—、—OC(═O)NRA—、—NRAC(═O)O—或—NRA—，其中RA为氢或C1-C6烷基。p、r和s独立地为0或1。R1表示式-(Alk3)a-(Y)b-(Alk4)d-B的基团，其中a、b和d独立地为0或1；Alk3和Alk4是可选取代的二价C,-C3烷基基团；Y表示具有5至8个环原子的单环二价碳环或杂环基、—O—、—S—或—NRA—，其中RA为氢或C1-C6烷基；B表示氢或卤素，或者具有5至8个环原子的可选取代单环碳环或杂环环，或者在Y为—NRA—且b为1的情况下，RA和式-(Alk4)d-B与它们连接的氮一起可能形成可选取代的杂环环。R表示氢、卤素、C1-C6烷基、C1-C6烷氧基、C1-C6烷硫基、苯基、苄基、具有3至6个环原子的环烷基或具有5或6个环原子的单环杂环基。
• HETEROCYCLIC COMPOUNDS FOR USE IN THE TREATMENT OF PI3K-GAMMA MEDIATED DISORDERS
  申请人：Infinity Pharmaceuticals, Inc.

  公开号：EP4066834A1

  公开（公告）日：2022-10-05

  Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

  本文描述了调节激酶活性（包括 PI3 激酶活性）的化合物和药物组合物，以及治疗与激酶活性（包括 PI3 激酶活性）相关的疾病和病症的化合物、药物组合物和方法。
• Macrocyclic compounds and uses thereof
  申请人：TURNING POINT THERAPEUTICS, INC.

  公开号：US11155563B2

  公开（公告）日：2021-10-26

  The present disclosure relates to certain macrocyclic compounds that inhibit SRC and MET, and/or CSF1R, pharmaceutical compositions containing such compounds, and methods of using such compounds to treat cancer.

  本公开涉及某些抑制 SRC 和 MET 和/或 CSF1R 的大环化合物、含有此类化合物的药物组合物以及使用此类化合物治疗癌症的方法。