9-(2-bromoethyl)-2-(butyloxy)-8-(methyloxy)-9H-purin-6-amine | 866268-56-6

• 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: 9-(2-bromoethyl)-2-(butyloxy)-8-(methyloxy)-9H-purin-6-amine
• 英文别名: 9-(2-bromoethyl)-2-butoxy-8-methoxy-9H-purin-6-amine；9-(2-Bromoethyl)-2-butoxy-8-methoxyadenine；9-(2-bromoethyl)-2-butoxy-8-methoxypurin-6-amine
• CAS: 866268-56-6
• 化学式: C₁₂H₁₈BrN₅O₂
• 分子量: 344.211
• InChiKey: NOFKMZFATJRIQU-UHFFFAOYSA-N

物化性质

• 沸点：
  505.3±60.0 °C(Predicted)
• 密度：
  1.60±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  20
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.58
• 拓扑面积：
  88.1
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  9-(2-bromoethyl)-2-(butyloxy)-8-(methyloxy)-9H-purin-6-amine 、 C.I.酸性橙108 在 乙酸乙酯 、 ammonia methanol 作用下， 以 乙腈 为溶剂， 反应 24.0h， 生成 2-{[2-(6-amino-2-butoxy-8-methoxy-9H-purin-9-yl)ethyl]amino}ethanol
  参考文献：
  名称：

  9-Substituted 8-Oxoadenine Compound

  摘要：

  本发明提供了一种具有免疫调节活性的8-氧腺嘌呤化合物，例如干扰素诱导活性，并可用作抗病毒剂和抗过敏剂，其化学式表示为（1）：[其中环A代表6-10个成员的芳香环烃环等，R代表卤素原子，烷基等，n代表0-2的整数，Z1代表烷基，X2代表氧原子，硫原子，SO2，NR5，CO，CONR5，NR5CO等，Y1，Y2和Y3分别代表单键或烷基，X1代表氧原子，硫原子，NR4（R4为氢原子或烷基）或单键，R2代表取代或未取代的烷基，R1代表氢原子，羟基，烷氧基，烷氧羰基或卤代烷基]或其药学上可接受的盐。

  公开号：

  US20140045837A1
• 作为产物：
  描述：

  2-butoxy-8-methoxy-9H-purine-6-amine trifluoroacetic acid 、 1,2-二溴乙烷 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.0h， 生成 9-(2-bromoethyl)-2-(butyloxy)-8-(methyloxy)-9H-purin-6-amine
  参考文献：
  名称：

  [EN] PURINE DERIVATIVES FOR USE IN THE TREATMENT OF ALLERGIC, INFLAMMATORY AND INFECTIOUS DISEASES
  [FR] DÉRIVÉS PURINES DESTINÉS À ÊTRE UTILISÉS DANS LE TRAITEMENT DE MALADIES ALLERGIQUES, INFLAMMATOIRES ET INFECTIEUSES

  摘要：

  化合物的化学式（I）：其中R1是C1-6烷基氨基，C1-6烷氧基或C3-7环烷氧基；m是一个整数，取值为2到6；R2是氢，C1-6烷基或C3-7环烷基C0-6烷基；以及它们的盐是人类干扰素的诱导剂。诱导人类干扰素的化合物可能在治疗各种疾病方面有用，例如治疗过敏性疾病和其他炎症性疾病，例如过敏性鼻炎和哮喘，治疗传染病和癌症，也可能作为疫苗佐剂有用。

  公开号：

  WO2010018131A1

文献信息

• 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。
• 9-Substituted 8-oxoadenine compound
  申请人：Kurimoto Ayumu

  公开号：US20070190071A1

  公开（公告）日：2007-08-16

  The present invention provides an 8-oxoadenine compound having immunemodulating activities such as an interferon inducing activity and useful as an antiviral agent and antiallergic agent, which is represented by the following formula (1): [wherein the ring A represents a 6-10 membered aromatic carbocyclic ring and the like, R represents a halogen atom, an alkyl group and the like, n represents an integer of 0-2, Z 1 represents alkylene, X 2 represents oxygen atom, sulfur atom, SO 2 , NR 5 , CO, CONR 5 , NR 5 CO and the like, Y 1 , Y 2 and Y 3 represent independently a single bond or an alkylene group, X 1 represents oxygen atom, sulfur atom, NR 4 (R 4 is hydrogen atom or an alkyl group) or a single bond, R 2 represents a substituted or unsubstituted alkyl group, R 1 represents hydrogen atom, hydroxy group, an alkoxy group, an alkoxycarbonyl group or a haloalkyl group] or its pharmaceutically acceptable salt.

  本发明提供了一种具有免疫调节活性的8-氧腺嘌呤化合物，例如干扰素诱导活性，并且可用作抗病毒剂和抗过敏剂，其化学式如下（1）所示：[其中，环A代表6-10个成员的芳香环烷基环等，R代表卤素原子，烷基等，n代表0-2的整数，Z1代表烷基，X2代表氧原子，硫原子，SO2，NR5，CO，CONR5，NR5CO等，Y1，Y2和Y3独立地代表单键或烷基，X1代表氧原子，硫原子，NR4（R4为氢原子或烷基）或单键，R2代表取代或未取代的烷基，R1代表氢原子，羟基，烷氧基，烷氧羰基或卤代烷基]或其药学上可接受的盐。
• NOVEL ADENINE COMPOUND
  申请人：Millichip Ian

  公开号：US20090099216A1

  公开（公告）日：2009-04-16

  A novel adenine compound represented by the formula (1): wherein Z represents (un)substituted alkylene, a single bond, etc.; R 1 represents an (un)substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl group; R 2 represents hydrogen or (un)substituted alkyl; R 3 , R 4 and R 5 each independently represents an (un)substituted alkyl, alkenyl, alkynyl, aryl, or heteroaryl group, provided that R 3 and R 5 may be bonded to each other to form a 3- to 7-membered, saturated carbocycle or heterocycle in cooperation with the adjacent carbon atom; and X represents oxygen, sulfur, SO 2 , NR 6 (R 6 represents hydrogen or alkyl), or a single bond, or a pharmaceutically acceptable salt of the compound. The compound and salt are useful as a medicine.

  一种新型腺嘌呤化合物，由公式（1）表示：其中Z代表（未）取代的烷基，单键等；R1代表（未）取代的烷基，烯基，炔基，环烷基，芳基或杂环芳基；R2代表氢或（未）取代的烷基；R3、R4和R5各自独立地表示（未）取代的烷基，烯基，炔基，芳基或杂环芳基，但R3和R5可以与相邻的碳原子合作形成3-至7-环的饱和碳环或杂环；X代表氧，硫，SO2，NR6（R6代表氢或烷基）或单键，或化合物的药学上可接受的盐。该化合物和盐可用作药物。
• 9-substituted 8-oxoadenine compound
  申请人：Dainippon Sumitomo Pharma Co., Ltd.

  公开号：US08012964B2

  公开（公告）日：2011-09-06

  The present invention provides an 8-oxoadenine compound having immunemodulating activities such as an interferon inducing activity and useful as an antiviral agent and antiallergic agent, which is represented by the following formula (1): [wherein the ring A represents a 6-10 membered aromatic carbocyclic ring and the like, R represents a halogen atom, an alkyl group and the like, n represents an integer of 0-2, Z1 represents alkylene, X2 represents oxygen atom, sulfur atom, SO2, NR5, CO, CONR5, NR5CO and the like, Y1, Y2 and Y3 represent independently a single bond or an alkylene group, X1 represents oxygen atom, sulfur atom, NR4 (R4 is hydrogen atom or an alkyl group) or a single bond, R2 represents a substituted or unsubstituted alkyl group, R1 represents hydrogen atom, hydroxy group, an alkoxy group, an alkoxycarbonyl group or a haloalkyl group] or its pharmaceutically acceptable salt.

  本发明提供了一种具有免疫调节活性的8-氧腺嘌呤化合物，例如具有干扰素诱导活性，可用作抗病毒剂和抗过敏剂，其化学式如下所示（1）：[其中环A代表6-10成员的芳香环烃环等，R代表卤素原子，烷基等，n代表0-2的整数，Z1代表烷基，X2代表氧原子，硫原子，SO2，NR5，CO，CONR5，NR5CO等，Y1，Y2和Y3分别代表单键或烷基，X1代表氧原子，硫原子，NR4（R4为氢原子或烷基）或单键，R2代表取代或未取代的烷基，R1代表氢原子，羟基，烷氧基，烷氧羰基或卤代烷基]或其药学上可接受的盐。
• PURINE DERIVATIVES FOR USE IN THE TREATMENT OF ALLERGIC, INFLAMMATORY AND INFECTIOUS DISEASES
  申请人：Bazin-Lee Helene

  公开号：US20110135671A1

  公开（公告）日：2011-06-09

  The present invention relates to compounds of formula (I): wherein R 1 is C 1-6 alkylamino, C 1-6 alkoxy, or C 3-7 cycloalkyloxy; m is an integer having a value of 2 to 6; R 2 is hydrogen, C 1-6 alkyl, or C 3-7 cycloalkylC 0-6 alkyl; and salts thereof are inducers of human interferon. Compounds which induce human interferon may be useful in the treatment of various disorders, for example the treatment of allergic diseases and other inflammatory conditions for example allergic rhinitis and asthma, the treatment of infectious diseases and cancer, and may also be useful as vaccine adjuvants.

  本发明涉及式(I)的化合物：其中R1是C1-6烷基氨基，C1-6烷氧基或C3-7环烷氧基；m是一个整数，其值为2到6；R2是氢，C1-6烷基或C3-7环烷基C0-6烷基；以及它们的盐是人干扰素的诱导剂。诱导人干扰素的化合物可能在治疗各种疾病方面有用，例如治疗过敏性疾病和其他炎症性疾病，例如过敏性鼻炎和哮喘，治疗传染病和癌症，也可能作为疫苗佐剂有用。