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9-tert-butyl-9H-purine | 18202-63-6

中文名称
——
中文别名
——
英文名称
9-tert-butyl-9H-purine
英文别名
9-tert-butyl-9H-purine;9-Tertiaerbutylpurin (1c);9-t-Butyl-purin;9-Tert-butylpurine
9-tert-butyl-9H-purine化学式
CAS
18202-63-6
化学式
C9H12N4
mdl
——
分子量
176.221
InChiKey
QBDFVPIORWMKGT-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    43.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    1,3,5-三嗪methyl N-(cyanomethyl)methanimidate叔丁胺二氯甲烷 为溶剂, 反应 2.0h, 以37%的产率得到9-tert-butyl-9H-purine
    参考文献:
    名称:
    1-取代-1 H-咪唑-5-胺与1,3,5-三嗪的电子逆需求Diels-Alder反应,可有效合成嘌呤
    摘要:
    1,3,5-三嗪和2,4,6-三(三氟甲基)-1,3,5-三嗪与原位生成的1-取代的5-氨基-1 H-咪唑的反应导致一组官能化嘌呤。所开发的实用途径可作为制备相关ADA抑制剂的基础。
    DOI:
    10.1016/j.tet.2011.08.082
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文献信息

  • LOCKED NUCLEIC ACID CYCLIC DINUCLEOTIDE COMPOUNDS AND USES THEREOF
    申请人:ADURO BIOTECH, INC.
    公开号:US20190185511A1
    公开(公告)日:2019-06-20
    The present invention provides highly active locked nucleic acid cyclic-dinucleotide (LNA-CDN) immune stimulators that activate DCs via the cytoplasmic receptor known as STING (Stimulator of Interferon Genes). In particular, the LNA-CDNs of the present invention are provided in the form of a composition comprising one or more cyclic dinucleotides that induce human STING-dependent type I interferon production, wherein the cyclic dinucleotides present in the composition have at least one 2′, 4′ locked nucleic acids within the cyclic dinucleotide.
    本发明提供了高活性的锁定核酸环二核苷酸(LNA-CDN)免疫刺激剂,通过细胞质受体STING(干扰素基因刺激剂)激活DCs。具体而言,本发明的LNA-CDNs以一种组合物的形式提供,该组合物包括一种或多种诱导人类STING依赖型I型干扰素产生的环二核苷酸,其中组合物中的环二核苷酸至少有一个2′, 4′锁定核酸。
  • CATALYSTS AND METHODS FOR POLYMER SYNTHESIS
    申请人:NOVOMER, INC.
    公开号:US20130144032A1
    公开(公告)日:2013-06-06
    The present invention provides unimolecular metal complexes having increased activity in the copolymerization of carbon dioxide and epoxides. Also provided are methods of using such metal complexes in the synthesis of polymers. According to one aspect, the present invention provides metal complexes comprising an activating species with co-catalytic activity tethered to a multidentate ligand that is coordinated to the active metal center of the complex.
    本发明提供了在二氧化碳和环氧化物的共聚合中具有增强活性的单分子金属配合物。还提供了使用这种金属配合物在合成聚合物中的方法。根据一个方面,本发明提供了包括与具有共催化活性的活化物种相耦合的多齿配体的金属配合物,该多齿配体与复合物的活性金属中心配位。
  • Catalysts for polycarbonate production
    申请人:Saudi Aramco Technologies Company
    公开号:US11185853B2
    公开(公告)日:2021-11-30
    The present invention provides unimolecular metal complexes having increased activity in the copolymerization of carbon dioxide and epoxides. Also provided are methods of using such metal complexes in the synthesis of polymers. According to one aspect, the present invention provides metal complexes comprising an activating species with catalytic activity tethered to a ligand that is coordinated to the active metal center of the complex.
    本发明提供了在二氧化碳和环氧化物的共聚合中具有增强活性的单分子金属配合物。还提供了使用这种金属配合物在聚合物合成中的方法。根据一个方面,本发明提供了包含一个具有催化活性的活化物种,该活化物种被系到与复合物的活性金属中心配位的配体的金属配合物。
  • PROCESS FOR PREPARING [(3-HYDROXYPYRIDINE-2-CARBONYL)AMINO]ALKANOIC ACIDS, ESTERS AND AMIDES
    申请人:Lanthier Christopher M.
    公开号:US20120309977A1
    公开(公告)日:2012-12-06
    Disclosed are processes for preparing [(3-hydroxypyridine-2-carbonyl)amino]-alkanoic acids, derivatives, inter alia, 5-aryl substituted and 5-heteroaryl substituted [(3-hydroxypyridine-2-carbonyl]aminolacetic acids. Further disclosed are methods for making prodrugs of [(3-hydroxypyridine-2-carbonyl)-amino]acetic acids, for example, [(3-hydroxypyridine-2-carbonyl]amino}acetic acid esters and [3-hydroxypyridine-2-carbonyl]amino}acetic acid amides. The disclosed compounds are useful as prolyl hydroxylase inhibitors or for treating conditions wherein prolyl hydroxylase inhibition is desired.
    本发明揭示了制备[(3-羟基吡啶-2-羰基)氨基]-烷基酸的方法,其中包括5-芳基取代和5-杂环取代的[(3-羟基吡啶-2-羰基)氨基]乙酸衍生物。此外,还揭示了制备[(3-羟基吡啶-2-羰基)-氨基]乙酸的前药的方法,例如[(3-羟基吡啶-2-羰基)氨基]乙酸酯和[(3-羟基吡啶-2-羰基)氨基]乙酸酰胺。这些揭示的化合物可用作脯氨酸羟化酶抑制剂,或用于治疗需要脯氨酸羟化酶抑制的疾病。
  • Shape memory polymers
    申请人:Anthamatten Mitchell L.
    公开号:US20080177303A1
    公开(公告)日:2008-07-24
    The present disclosure relates to Shape Memory Polymers (SMP's) comprising function groups that allow the polymers to be elastically deformed, utilized in the elastically deformed state, and subsequently returned to the original polymorphic shape.
    本公开涉及形状记忆聚合物(SMP),其中包含允许聚合物弹性变形的功能基团,可在弹性变形状态下使用,并随后返回到原始的多态形状。
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