8-Methoxy-2-(2-methoxyethoxy)-9H-purine-6-amine | 930778-36-2

• 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-Methoxy-2-(2-methoxyethoxy)-9H-purine-6-amine
• 英文别名: 8-Methoxy-2-(2-methoxyethoxy)adenine；8-methoxy-2-(2-methoxyethoxy)-7H-purin-6-amine
• CAS: 930778-36-2
• 化学式: C₉H₁₃N₅O₃
• 分子量: 239.234
• InChiKey: JWTIKNIKDLTZCL-UHFFFAOYSA-N

物化性质

• 沸点：
  487.6±55.0 °C(Predicted)
• 密度：
  1.397±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  17
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  108
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  8-Methoxy-2-(2-methoxyethoxy)-9H-purine-6-amine 、 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 11.0h， 以69%的产率得到1,1-dimethylethyl 4-[(6-amino-2-(2-methoxyethoxy)-8-methoxy-9H-purin-9-yl)methyl]-1-piperidinecarboxylate
  参考文献：
  名称：

  EP1939199

  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。
• 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：Isobe Yoshiaki

  公开号：US20100099870A1

  公开（公告）日：2010-04-22

  A novel adenine compound represented by the formula (1): [wherein R 1 is substituted or unsubstituted alkyl, etc., X is oxygen, etc., A 1 is 4- to 8-membered substituted or unsubstituted saturated nitrogen-containing heterocycle containing 1 to 2 hetero atom(s) selected from 1 to 2 nitrogen(s), 0 to 1 oxygen and 0 to 1 sulfur, etc., A 2 is substituted or unsubstituted 6- to 10-membered aryl, etc., L 1 and L 2 are independently a straight chain or branched chain alkylene, etc.], or a pharmaceutically acceptable salt thereof, which is useful as a medicament.

  一种新型腺嘌呤化合物，其化学式为(1)：[其中R1是取代或未取代的烷基等，X是氧等，A1是4-至8-成员的取代或未取代的饱和含氮杂环，其中含有1至2个来自1至2个氮原子、0至1个氧原子和0至1个硫原子的杂原子等，A2是取代或未取代的6-至10-成员的芳基等，L1和L2是独立的直链或支链烷基等]，或其药学上可接受的盐，其用作药物。
• PURINE DERIVATIVES AS IMMUNOMODULATORS
  申请人：Lazarides Linos

  公开号：US20100120799A1

  公开（公告）日：2010-05-13

  Compounds of formula (I): wherein R 1 is C 1-8 alkylamino, C 1-8 alkoxy, C 3-7 cycloalkylC 1-6 alkylamino, C 3-7 cycloalkylC 1-6 alkoxy, C 1-3 alkoxyC 2-3 alkoxy, or Het b -C 1-3 alkoxy; Het b is a 5- or 6-membered saturated aliphatic heterocycle containing one oxygen atom; R 2 is —(CH 2 ) n -Het; n is an integer having a value of 1 to 4; Het is a 5- or 6-membered saturated aliphatic heterocycle containing one oxygen heteroatom, which heterocycle may be substituted by one or two C 1-4 alkyl groups, and salts and solvates thereof, are inducers of human interferon and may be useful in the treatment of various disorders in particular infectious diseases, cancer, and allergic diseases and other inflammatory conditions for example allergic rhinitis and asthma, and as vaccine adjuvants.

  化合物的式子(I)：其中R1是C1-8烷基氨基，C1-8烷氧基，C3-7环烷基C1-6烷基氨基，C3-7环烷基C1-6烷氧基，C1-3烷氧基C2-3烷氧基或Hetb-C1-3烷氧基；Hetb是含有一个氧原子的5-或6-成员饱和脂肪族杂环；R2是—(CH2)n-Het；n是一个值为1到4的整数；Het是含有一个氧杂原子的5-或6-成员饱和脂肪族杂环，该杂环可能被一个或两个C1-4烷基基团取代，以及其盐和溶剂化物，是人类干扰素的诱导剂，可用于治疗各种疾病，特别是感染性疾病、癌症、过敏性疾病和其他炎症状况，例如过敏性鼻炎和哮喘，并作为疫苗佐剂。
• COMPOUNDS
  申请人：Lazarides Linos

  公开号：US20110269781A1

  公开（公告）日：2011-11-03

  The present invention includes novel compounds useful in the treatment of various disorders in particular infectious diseases, cancer, and allergic diseases and other inflammatory conditions for example allergic rhinitis and asthma, and as vaccine adjuvants.

  本发明涵盖了新型化合物，可用于治疗各种疾病，特别是感染性疾病、癌症、过敏性疾病和其他炎症病症，例如过敏性鼻炎和哮喘，并可用作疫苗佐剂。