8-bromo-2-butoxyadenine | 866231-28-9

• 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: 8-bromo-2-butoxyadenine
• 英文别名: 8-bromo-2-butoxy-7H-purin-6-amine
• CAS: 866231-28-9
• 化学式: C₉H₁₂BrN₅O
• 分子量: 286.131
• InChiKey: ZVJSYAZFTPTGHC-UHFFFAOYSA-N

物化性质

• 沸点：
  513.3±60.0 °C(Predicted)
• 密度：
  1.648±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  89.7
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  8-bromo-2-butoxyadenine 、 1-BOC-4-甲磺酰基氧甲基哌啶 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 以74%的产率得到8-bromo-2-butoxy-9-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)adenine
  参考文献：
  名称：

  EP1939199

  摘要：

  公开号：
• 作为产物：
  描述：

  8-bromo-2-butoxy-9-(4-acetoxybenzyl)adenine 在 甲醇 、 sodium hydroxide 、 水 、 盐酸 作用下， 以 甲醇 为溶剂， 反应 4.0h， 以81%的产率得到8-bromo-2-butoxyadenine
  参考文献：
  名称：

  EP1728792

  摘要：

  公开号：

文献信息

• MODULATORS OF TOLL-LIKE RECEPTORS
  申请人：Halcomb Randall L.

  公开号：US20110098248A1

  公开（公告）日：2011-04-28

  The present application includes novel modulators of TLRs, compositions containing such compounds, therapeutic methods that include the administration of such compounds.

  本申请涵盖了TLR的新型调节剂，包含这类化合物的组合物，以及包括这类化合物的给药的治疗方法。
• 8-Oxoadenine Compound
  申请人：Ogita Haruhisa

  公开号：US20070225303A1

  公开（公告）日：2007-09-27

  An 8-oxoadenine compound useful as an immuno-modulator having specific activity against Th1/Th2, specifically a prophylactic and therapeutic agent for a topical application for allergic diseases, viral diseases and cancers, which is represented by the following formula (1): wherein A is a group of a formula represented by the formula (2): wherein R 2 is a substituted or unsubstituted alkyl group and so on, R 3 is hydrogen atom or an alkyl group, R is a halogen atom and so on, n is 0˜2, X 1 is oxygen atom, Z is straight or branched chain alkylene, and R 1 is an alkyl group which is optionally substituted by hydroxy group, an alkoxy group, alkoxycarbonyl group and so on, or its pharmaceutically acceptable salt.

  一种8-氧腺嘌呤化合物，可用作免疫调节剂，对Th1 / Th2具有特定活性，特别是用于过敏性疾病，病毒性疾病和癌症的局部应用的预防和治疗剂，其化学式（1）如下：其中A是由式（2）表示的式的基团：其中R2是取代或未取代的烷基基团等，R3是氢原子或烷基基团，R是卤素原子等，n为0〜2，X1为氧原子，Z为直链或支链烷基，R1为烷基基团，可选地由羟基基团，烷氧基基团，烷氧羰基基团等取代，或其药学上可接受的盐。
• Novel Adenine Compound
  申请人：Hashimoto Kazuki

  公开号：US20080269240A1

  公开（公告）日：2008-10-30

  An adenine compound useful as a medicine represented by the following formula (1): [wherein R 1 is halogen atom, optionally substituted alkyl group, optionally substituted aryl group, etc.; X is oxygen atom, sulfur atom, a single bond, etc.; A 1 is optionally substituted and optionally saturated 4 to 8 membered heterocyclic group containing 1 to 2 hetero atoms selected from 1 to 3 nitrogen atoms, 0 to 1 oxygen atom, and 0 to 1 sulfur atom; A 2 is optionally substituted 6 to 10 cyclic aromatic hydrocarbon group or optionally substituted 5 to 10 membered heterocyclic aromatic group; L 1 and L 2 are independently, substituted straight or branched alkylene or a single bond, etc.; L 3 is optionally substituted straight or branched alkylene, etc.; R 2 is hydrogen atom, optionally substituted alkyl group.] or its pharmaceutically acceptable salt.

  以下式子（1）所表示的一种腺嘌呤化合物，可用作药物：[其中，R1是卤素原子、可选取代烷基、可选取代芳基等；X是氧原子、硫原子、单键等；A1是可选取代和可饱和的4至8元杂环基，包含1至2个从1至3个氮原子、0至1个氧原子和0至1个硫原子中选取的杂原子；A2是可选取代的6至10环芳烃基或可选取代的5至10元杂环芳烃基；L1和L2是独立的、取代的直链或支链烷基或单键等；L3是可选取代的直链或支链烷基等；R2是氢原子、可选取代烷基等。]或其药学上可接受的盐。
• NOVEL ADENINE COMPOUND
  申请人：Hashimoto Kazuki

  公开号：US20090192153A1

  公开（公告）日：2009-07-30

  An adenine compound or its pharmaceutically acceptable salt as a medicament as shown following formula (1): wherein R 1 is optionally substituted alkyl group, etc., X is oxygen atom, etc., A is 4 to 8 membered optionally substituted saturated or unsaturated heterocyclic group containing 1 to 2 hetero atoms selected from 1 to 3 nitrogen atoms, 0 to 1 oxygen atom and 0 to 1 sulfur atom, L 1 and L 2 are independently straight or branched chain alkylene, or a single bond, R 2 is optionally substituted alkyl group, etc.

  一种腺嘌呤化合物或其药学上可接受的盐作为药物，如下所示的公式（1）：其中，R1是可选的取代烷基等，X是氧原子等，A是4到8个成员的可选取代饱和或不饱和杂环基团，包含1到2个杂原子，选自1到3个氮原子，0到1个氧原子和0到1个硫原子，L1和L2是独立的直链或支链烷基，或单键，R2是可选的取代烷基等。
• 8-OXOADENINE COMPOUND
  申请人：Dainippon Sumitomo Pharma Co., Ltd.

  公开号：EP1728792A1

  公开（公告）日：2006-12-06

  An 8-oxoadenine compound useful as an immuno-modulator having specific activity against Th1/Th2, specifically a prophylactic and therapeutic agent for a topical application for allergic diseases, viral siseases and cancers, which is represented by the following formula (1): , wherein A is a group of a formula represented by the formula (2): , wherein R2 is a substituted or unsubstituted alkyl group and so on, R3 is hydrogen atom or an alkyl group, R is a halogen atom and so on, n is 0-2, X1 is oxygen atom, Z is straight or branched chain alkylene, and R1 is an alkyl group which is optionally substituted by hydroxy group, an alkoxy group, alkoxycarbonyl group and so on, or its pharmaceutically acceptable salt.

  一种 8-氧代腺嘌呤化合物，可用作对 Th1/Th2 具有特异性活性的免疫调节剂，特别是用于过敏性疾病、病毒性疾病和癌症的局部预防和治疗剂，由下式（1）表示： 其中 A 是由式（2）表示的一个式组： 其中 R2 是取代或未取代的烷基等，R3 是氢原子或烷基，R 是卤素原子等、 n 为 0-2、 X1 是氧原子，Z 是直链或支链亚烷基，R1 是可选被羟基、烷氧基、烷氧羰基等取代的烷基、 或其药学上可接受的盐。