3,3-二甲基-6-硝基-2,3-二氢-1H-异吲哚-1-酮 | 1214900-72-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 中文名称: 3,3-二甲基-6-硝基-2,3-二氢-1H-异吲哚-1-酮
• 英文名称: 3,3-dimethyl-6-nitro-2,3-dihydro-1H-isoindol-1-one
• 英文别名: 3,3-dimethyl-6-nitroisoindolin-1-one；3,3-dimethyl-6-nitro-2H-isoindol-1-one
• CAS: 1214900-72-7
• 化学式: C₁₀H₁₀N₂O₃
• 分子量: 206.201
• InChiKey: LQWDYKNVIZRQSN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  74.9
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3,3-二甲基-6-硝基-2,3-二氢-1H-异吲哚-1-酮 在 sodium hydroxide 、 diborane(6) 作用下， 以 四氢呋喃 、 甲醇 、 水 为溶剂， 以83.1 %的产率得到1,1-dimethyl-5-nitro-2,3-dihydro-1H-isoindole
  参考文献：
  名称：

  [EN] TETRAHYDROPYRIDO[3,4-D]PYRIMIDINES COMPOUNDS AS HPK1 INHIBITORS
  [FR] COMPOSÉS DE TÉTRAHYDROPYRIDO[3,4-D]PYRIMIDINES UTILISÉS EN TANT QU'INHIBITEURS DE HPK1

  摘要：

  Tetrahydropyrido[3,4-d]pyrimidine compounds are provided that are potent HPK1 inhibitors. The compounds are useful to treat or prevent cancer and/or inflammatory and/or autoimmune diseases or symptoms thereof in mammals, particularly humans. The compounds have a chemical structure of the general Formula (I), (II), (III), (IV) or (V) or enantiomers or diastereomers or mixtures thereof or pharmaceutically acceptable salts thereof.

  公开号：

  WO2023220541A1
• 作为产物：
  描述：

  2,3-二氢-3,3-二甲基-1H-异吲哚-1-酮 在 硫酸 、 potassium nitrate 作用下， 以92.1 %的产率得到3,3-二甲基-6-硝基-2,3-二氢-1H-异吲哚-1-酮
  参考文献：
  名称：

  [EN] TETRAHYDROPYRIDO[3,4-D]PYRIMIDINES COMPOUNDS AS HPK1 INHIBITORS
  [FR] COMPOSÉS DE TÉTRAHYDROPYRIDO[3,4-D]PYRIMIDINES UTILISÉS EN TANT QU'INHIBITEURS DE HPK1

  摘要：

  Tetrahydropyrido[3,4-d]pyrimidine compounds are provided that are potent HPK1 inhibitors. The compounds are useful to treat or prevent cancer and/or inflammatory and/or autoimmune diseases or symptoms thereof in mammals, particularly humans. The compounds have a chemical structure of the general Formula (I), (II), (III), (IV) or (V) or enantiomers or diastereomers or mixtures thereof or pharmaceutically acceptable salts thereof.

  公开号：

  WO2023220541A1

文献信息

• AMINOTRIAZOLOPYRIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
  申请人：Bahmanyar Sogole

  公开号：US20100093698A1

  公开（公告）日：2010-04-15

  Provided herein are Heteroaryl Compounds of formula (I): wherein R 1 and R 2 are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing inflammatory conditions or cancer, and conditions treatable or preventable by inhibition of a kinase or a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a subject in need thereof.

  本文提供了公式（I）的杂环芳基化合物：其中R1和R2如本文所定义，包含有效量杂环芳基化合物的组合物，以及用于治疗或预防炎症性疾病或癌症的方法，以及通过抑制激酶或激酶途径治疗或预防的疾病，包括向需要的受试者施用有效量杂环芳基化合物。
• AMINOTRIAZOLOPYRIDINES AND THEIR USE AS KINASE INHIBITORS
  申请人：Signal Pharmaceuticals, LLC

  公开号：EP2344494A1

  公开（公告）日：2011-07-20
• US8299056B2
  申请人：——

  公开号：US8299056B2

  公开（公告）日：2012-10-30
• [EN] AMINOTRIAZOLOPYRIDINES AND THEIR USE AS KINASE INHIBITORS<br/>[FR] AMINOTRIAZOLOPYRIDINES ET LEUR UTILISATION COMME INHIBITEURS DE KINASE
  申请人：SIGNAL PHARM LLC

  公开号：WO2010027500A1

  公开（公告）日：2010-03-11

  Provided herein are Heteroaryl Compounds of formula (I): wherein R1 and R2 are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing inflammatory conditions or cancer, and conditions treatable or preventable by inhibition of a kinase or a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a subject in need thereof.
• [EN] TETRAHYDROPYRIDO[3,4-D]PYRIMIDINES COMPOUNDS AS HPK1 INHIBITORS<br/>[FR] COMPOSÉS DE TÉTRAHYDROPYRIDO[3,4-D]PYRIMIDINES UTILISÉS EN TANT QU'INHIBITEURS DE HPK1
  申请人：[en]MERCK PATENT GMBH

  公开号：WO2023220541A1

  公开（公告）日：2023-11-16

  Tetrahydropyrido[3,4-d]pyrimidine compounds are provided that are potent HPK1 inhibitors. The compounds are useful to treat or prevent cancer and/or inflammatory and/or autoimmune diseases or symptoms thereof in mammals, particularly humans. The compounds have a chemical structure of the general Formula (I), (II), (III), (IV) or (V) or enantiomers or diastereomers or mixtures thereof or pharmaceutically acceptable salts thereof.