2-butoxy-9-(6-chloro-3-pyridylmethyl)adenine | 473930-53-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: 2-butoxy-9-(6-chloro-3-pyridylmethyl)adenine
• 英文别名: 2-butoxy-9-(6-chloropyridin-3-ylmethyl)adenine；2-butoxy-9-[(6-chloropyridin-3-yl)methyl]purin-6-amine
• CAS: 473930-53-9
• 化学式: C₁₅H₁₇ClN₆O
• 分子量: 332.793
• InChiKey: UJLVAEAMOZGIEG-UHFFFAOYSA-N

物化性质

• 沸点：
  594.3±60.0 °C(Predicted)
• 密度：
  1.44±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  23
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  91.7
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-butoxy-9-(6-chloro-3-pyridylmethyl)adenine 在 盐酸 、 水 、 溴 作用下， 以 二氯甲烷 为溶剂， 反应 47.17h， 生成 6-amino-9-((6-(4-(2-aminoethyl)piperidin-1-yl)pyridin-3-yl)methyl)-2-butoxy-7H-purin-8(9H)-one
  参考文献：
  名称：

  [EN] ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF
  [FR] CONJUGUÉS ANTICORPS-AGONISTES DE TLR, PROCÉDÉS ET UTILISATIONS DE CEUX-CI

  摘要：

  本文披露了TLR-激动剂化合物、抗体-TLR激动剂结合物、制药组合物以及使用这些化合物或结合物作为治疗癌症等疾病或病症的治疗剂的方法。

  公开号：

  WO2022040596A1
• 作为产物：
  描述：

  2,6-二氯-9-(四氢-2H-吡喃-2-基)-9h-嘌呤 在 氨 、 potassium carbonate 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 47.5h， 生成 2-butoxy-9-(6-chloro-3-pyridylmethyl)adenine
  参考文献：
  名称：

  [EN] ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF
  [FR] CONJUGUÉS ANTICORPS-AGONISTES DE TLR, PROCÉDÉS ET UTILISATIONS DE CEUX-CI

  摘要：

  本文披露了TLR-激动剂化合物、抗体-TLR激动剂结合物、制药组合物以及使用这些化合物或结合物作为治疗癌症等疾病或病症的治疗剂的方法。

  公开号：

  WO2022040596A1

文献信息

• Novel adenne derivatives
  申请人：——

  公开号：US20040132748A1

  公开（公告）日：2004-07-08

  This invention relates to an adenine derivative, a tautomer thereof, or a pharmaceutically acceptable salt thereof represented by general formula (I): 1 wherein X represents NR 3 (wherein R 3 represents a hydrogen atom or C 1-3 alkyl) or the like; R 1 represents substituted or unsubstituted alkyl or the like; R 2 represents hydroxyl or the like; and Y represents a substituted or unsubstituted aromatic hetero ring or the like. Also, the present invention relates to pharmaceuticals such as an interferon inducer, antiviral agent, anticancer agent, type 2 helper T cell selective immune response inhibitor, antiallergic agent, and immune response modulator comprising the above derivative as an active ingredient.

  本发明涉及一种由通式（I）表示的腺嘌呤衍生物、其互变异构体或其药学上可接受的盐，其中X代表NR3（其中R3代表氢原子或C1-3烷基）或类似物；R1代表取代或未取代的烷基或类似物；R2代表羟基或类似物；Y代表取代或未取代的芳香杂环或类似物。此外，本发明还涉及将上述衍生物作为活性成分的药物，例如干扰素诱导剂、抗病毒剂、抗癌剂、2型辅助T细胞选择性免疫反应抑制剂、抗过敏剂和免疫反应调节剂。
• Adenine derivatives
  申请人：Dainippon Simitomo Pharma Co., Ltd.

  公开号：US07157465B2

  公开（公告）日：2007-01-02

  This invention relates to an adenine derivative, a tautomer thereof, or a pharmaceutically acceptable salt thereof represented by general formula (I): wherein X represents NR3 (wherein R3 represents a hydrogen atom or C1-3 alkyl) or the like; R1 represents substituted or unsubstituted alkyl or the like; R2 represents hydroxyl or the like; and Y represents a substituted or unsubstituted aromatic hetero ring or the like. Also, the present invention relates to pharmaceuticals such as an interferon inducer, antiviral agent, anticancer agent, type 2 helper T cell selective immune response inhibitor, antiallergic agent, and immune response modulator comprising the above derivative as an active ingredient.

  本发明涉及一种腺嘌呤衍生物、其互变异构体或其药学上可接受的盐，其通式表示为（I）：其中X代表NR3（其中R3代表氢原子或C1-3烷基）或类似物；R1代表取代或未取代的烷基或类似物；R2代表羟基或类似物；Y代表取代或未取代的芳香杂环或类似物。此外，本发明还涉及一种以上述衍生物为活性成分的药物，例如干扰素诱导剂、抗病毒剂、抗癌剂、第二型辅助T细胞选择性免疫反应抑制剂、抗过敏剂和免疫反应调节剂。
• Novel adenine derivatives
  申请人：Isobe Yoshiaki

  公开号：US20070037832A1

  公开（公告）日：2007-02-15

  This invention relates to an adenine derivative, a tautomer thereof, or a pharmaceutically acceptable salt thereof represented by general formula (I): wherein X represents NR 3 (wherein R 3 represents a hydrogen atom or C 1-3 alkyl) or the like; R 1 represents substituted or unsubstituted alkyl or the like; R 2 represents hydroxyl or the like; and Y represents a substituted or unsubstituted aromatic hetero ring or the like. Also, the present invention relates to pharmaceuticals such as an interferon inducer, antiviral agent, anticancer agent, type 2 helper T cell selective immune response inhibitor, antiallergic agent, and immune response modulator comprising the above derivative as an active ingredient.

  本发明涉及一种腺嘌呤衍生物，其互变异构体或药学上可接受的盐，由下式表示：其中X代表NR3（其中R3代表氢原子或C1-3烷基）或类似物；R1代表取代或未取代的烷基或类似物；R2代表羟基或类似物；Y代表取代或未取代的芳香杂环或类似物。此外，本发明涉及上述衍生物作为活性成分的制备干扰素诱导剂、抗病毒剂、抗癌剂、选择性抑制2型辅助T细胞免疫反应抑制剂、抗过敏剂和免疫反应调节剂等药物。
• NOVEL ADENINE COMPOUND
  申请人：Isobe Yoshiaki

  公开号：US20090105212A1

  公开（公告）日：2009-04-23

  A novel adenine compound represented by the formula (1): wherein A represents an (un)substituted aromatic carbocycle or (un)substituted aromatic heterocycle; L 1 , L 2 , and L 3 each independently represents linear or branched alkylene, etc.; R 1 represents (un)substituted alkyl, (un)substituted aryl, etc.; R 2 represents hydrogen or (un) substituted alkyl; R 3 represents (un)substituted alkyl, etc., provided that R 3 may be bonded to L 2 or L 3 to form a nitrogenous saturated heterocycle; and X represents oxygen, etc.; or a pharmaceutically acceptable salt of the compound. The compound and salt are useful as a medicine.

  一种新型腺嘌呤类化合物，其化学式为（1）：其中A代表（未）取代芳香族碳环或（未）取代芳香族杂环；L1，L2和L3分别独立地代表线性或支链烷基等；R1代表（未）取代烷基，（未）取代芳基等；R2代表氢或（未）取代烷基；R3代表（未）取代烷基等，但R3可与L2或L3结合形成含氮饱和杂环；X代表氧等；或该化合物的药学上可接受的盐。该化合物和盐作为药物有用。
• Novel Adenine Compound
  申请人：Hashimoto Kazuki

  公开号：US20090118263A1

  公开（公告）日：2009-05-07

  An adenine compound represented by the formula (1): (1) [wherein A 1 and A 2 each independently represents an (un)substituted aromatic carbocycle or (un)substituted aromatic heterocycle; L 1 , L 2 , and L 3 each independently represents alkylene or a single bond, provided that any methylene or methine group in L 2 or L 3 may be bonded to the nitrogen atom adjacent to L 2 and L 3 to form a 4- to 7-membered saturated nitrogenous heterocycle; L 4 represents alkylene or a single bond; R 1 represents (un)substituted alkyl, (un)substituted aryl, etc.; R 2 represents hydrogen or (un)substituted alkyl; R 3 represents (un)substituted alkyl, etc.; and X represents oxygen, etc.] or a pharmaceutically acceptable salt of the compound. The compound and salt are useful as a medicine.

  一种腺嘌呤化合物，由式（1）表示：（1）[其中A1和A2分别独立地表示（非）取代芳香族碳环或（非）取代芳香族杂环；L1、L2和L3分别独立地表示烷基或单键，但L2或L3中的任何亚甲基或亚胺基可能与L2和L3相邻的氮原子结合形成4-至7元饱和的氮杂环；L4表示烷基或单键；R1表示（非）取代烷基、（非）取代芳基等；R2表示氢或（非）取代烷基；R3表示（非）取代烷基等；X表示氧等]或该化合物的药物可接受的盐。该化合物和盐可用作药物。