3-(aminomethyl)-N,N-dimethylpyridin-2-amine | 354824-09-2

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 3-(aminomethyl)-N,N-dimethylpyridin-2-amine
• CAS: 354824-09-2
• 化学式: C₈H₁₃N₃
• mdl: MFCD09731450
• 分子量: 151.211
• InChiKey: LRMLNAXJNYRHHZ-UHFFFAOYSA-N

物化性质

• 沸点：
  271.2±30.0 °C(Predicted)
• 密度：
  1.075±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.375
• 拓扑面积：
  42.2
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2933399090

反应信息

• 作为反应物：
  描述：

  3-(aminomethyl)-N,N-dimethylpyridin-2-amine 、 ethyl 9-fluoro-7-hydroxy-3-methyl-5-oxo-2,3-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-6-carboxylate 以 N,N-二甲基甲酰胺 为溶剂， 反应 0.5h， 以85%的产率得到N-((2-(dimethylamino)pyridin-3-yl)methyl)-9-fluoro-7-hydroxy-3-methyl-5-oxo-2,3-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-6-carboxamide
  参考文献：
  名称：

  Identification of Human Toll-like Receptor 2-Agonistic Activity in Dihydropyridine–Quinolone Carboxamides

  摘要：

  Using a multiplexed, reporter gene-based, high throughput screen, we identified 9-fluoro-7-hydroxy-3-methyl-5-oxo-N-(pyridin-3-ylmethyl)-2,3-dihydro-1H,SH-pyrido- [3,2,1-ij]quinoline-6-carboxamide as a TLR2 agonist. Preliminary structure-activity relationship studies on the carboxamide moiety led to the identification of analogues that induce chemokines and cytokines in a TLR2-dependent manner. These results represent new leads for the development of vaccine adjuvants.

  DOI：

  10.1021/acsmedchemlett.8b00540
• 作为产物：
  描述：

  2-二甲氨基-3-氰基吡啶 在 aluminum nickel ammonium hydroxide 、 氢气 作用下， 以 乙醇 为溶剂， 生成 3-(aminomethyl)-N,N-dimethylpyridin-2-amine
  参考文献：
  名称：

  Fused imidazolium derivatives

  摘要：

  这项发明涉及药物，特别是用于治疗癌症的新型融合咪唑基衍生物，以及其新型合成中间化合物。这些新型咪唑基衍生物与芳基或杂环芳基环融合，其特征在于1-和/或3-位置被取代为具有从羟基、烷基等取代基中选择的取代基，具有出色的抗肿瘤活性和低毒性，并且作为具有广泛安全边界的抗癌剂而有用。

  公开号：

  US20030114508A1

文献信息

• HETEROCYCLIC COMPOUND HAVING ANTI-HIV ACTIVITY
  申请人：Toyama Chemical Co., Ltd.

  公开号：EP2810944A1

  公开（公告）日：2014-12-10

  A heterocyclic compound represented by the general formula (in the formula, R1, R2 and R3 may be the same or different, and each represents a hydrogen atom, a halogen atom, or this general formula (X1-Y1-R4) (in the formula: X1 represents this general formula (NR5) (in the formula, R5 represents a hydrogen atom, etc.) or the like; Y1 represents an optionally substituted C1-6 alkylene group or the like; and R4 represents an optionally substituted aryl group or the like), and Z represents a nitrogen atom or this general formula (CR6) (in the formula, R6 represents a hydrogen atom, a halogen atom, or an optionally substituted C1-12 alkyl group or the like)), or a salt thereof, exhibits excellent anti-HIV activity and is useful as an anti-HIV agent.

  由一般公式表示的杂环化合物（在公式中，R1、R2和R3可以相同也可以不同，每个表示氢原子、卤原子或这一般式（X1-Y1-R4）（在公式中：X1表示这一般式（NR5）（在公式中，R5表示氢原子等）或类似物；Y1表示可选择地取代的C1-6烷基链或类似物；R4表示可选择地取代的芳基或类似物），Z表示氮原子或这一般式（CR6）（在公式中，R6表示氢原子、卤原子或可选择地取代的C1-12烷基链或类似物）），或其盐，表现出优异的抗HIV活性，并可用作抗HIV剂。
• Fused imidazolium derivatives
  申请人：——

  公开号：US20030114508A1

  公开（公告）日：2003-06-19

  This invention relates to medicaments, particularly novel fused imidazolium derivatives useful for the treatment of cancers and novel synthetic intermediate compounds thereof. The novel imidazolium derivatives fused with an aryl or heteroaryl ring, characterized in that the 1- and/or 3-position is substituted by an alkyl group etc. having a substituent selected from the group consisting of —OR a , —SRa and the like, have excellent anti-tumor activity and low toxicity and are useful as anticancer agents having wide margins of safety. 1

  这项发明涉及药物，特别是用于治疗癌症的新型融合咪唑基衍生物，以及其新型合成中间化合物。这些新型咪唑基衍生物与芳基或杂环芳基环融合，其特征在于1-和/或3-位置被取代为具有从羟基、烷基等取代基中选择的取代基，具有出色的抗肿瘤活性和低毒性，并且作为具有广泛安全边界的抗癌剂而有用。
• FUSED IMIDAZOLIUM DERIVATIVES
  申请人：YAMANOUCHI PHARMACEUTICAL CO. LTD.

  公开号：EP1256576A1

  公开（公告）日：2002-11-13

  This invention relates to medicaments, particularly novel fused imidazolium derivatives useful for the treatment of cancers and novel synthetic intermediate compounds thereof. The novel imidazolium derivatives fused with an aryl or heteroaryl ring, characterized in that the 1- and/or 3-position is substituted by an alkyl group etc. having a substituent selected from the group consisting of -ORa, -SRa and the like, have excellent anti-tumor activity and low toxicity and are useful as anticancer agents having wide margins of safety.

  本发明涉及药物，特别是用于治疗癌症的新型融合咪唑鎓衍生物及其新型合成中间体化合物。 与芳基或杂芳基环融合的新型咪唑鎓衍生物，其特征在于1位和/或3位被烷基等取代，该烷基的取代基选自-ORa、-SRa等组成的组，具有优异的抗肿瘤活性和低毒性，可用作抗癌剂，具有较宽的安全范围。
• Therapeutic compounds and methods of use thereof
  申请人：Regents of the University of Minnesota

  公开号：US11014921B2

  公开（公告）日：2021-05-25

  The invention provides a compound of formula I: or a salt thereof, wherein R1, R2, and R3 have any of the values described in the specification, as well as compositions comprising a compound of formula I. The compounds are useful as immunomodulating agents.

  本发明提供了一种式 I 的化合物： 或其盐，其中 R1、R2 和 R3 具有说明书中描述的任一值，以及包含式 I 化合物的组合物。这些化合物可用作免疫调节剂。
• PYRIDAZINE COMPOUNDS FOR INHIBITING NAV1.8
  申请人：Lieber Institute, Inc.

  公开号：US20210139456A1

  公开（公告）日：2021-05-13

  Pyridazine compounds for inhibiting NaV1.8 and methods for treating a condition, disease, or disorder associated with an increased NaV1.8 activity or expression are disclosed.