摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-azido-furazan-3-amine | 1379659-25-2

中文名称
——
中文别名
——
英文名称
N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-azido-furazan-3-amine
英文别名
N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-3-yl)-4-azidofurazan-3-amine;N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-azidofurazan-3-amine;4-azido-N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-1,2,5-oxadiazol-3-amine
N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-azido-furazan-3-amine化学式
CAS
1379659-25-2
化学式
C5H2N12O
mdl
——
分子量
246.151
InChiKey
RACTZLAYMPRNQX-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):
    -0.2
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    134
  • 氢给体数:
    1
  • 氢受体数:
    11

反应信息

  • 作为产物:
    描述:
    4-azido-1,2,5-oxadiazol-3-amine6-(3,5-dimethylpyrazol-1-yl)-1,2,4-triazolo[4,3-b][1,2,4,5]tetrazinepotassium carbonate 作用下, 以 乙腈 为溶剂, 反应 4.0h, 以80%的产率得到N-([1,2,4]triazolo[4,3-b][1,2,4,5]tetrazin-6-yl)-4-azido-furazan-3-amine
    参考文献:
    名称:
    A Direct Approach to a 6-Hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazine Library
    摘要:
    The synthesis of 6-hetarylamino[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazines is reported. The functionalized secondary amines were constructed via a K2CO3-mediated SNAr reaction of weakly basic hetarylamines with 3-(3,5-dimethylpyrazol-1-yl)[1,2,4]triazolo[4,3-b][1,2,4,5]tetrazines, which allowed displacement 3,5-dimethylpyrazolyl leaving group. Significantly, the reaction exhibited a broad substrate scope and proceeded in good yields.
    DOI:
    10.1021/ol403308h
点击查看最新优质反应信息

文献信息

  • Copper-Catalyzed C-N Coupling Reactions of Nitrogen-Rich Compounds - Reaction of Iodofurazans with s-Tetrazinylamines
    作者:Aleksei B. Sheremetev、Nadezhda V. Palysaeva、Marina I. Struchkova、Kyrill Yu. Suponitsky、Mikhail Yu. Antipin
    DOI:10.1002/ejoc.201101732
    日期:2012.4
    Access to unsymmetrical secondary dihetarylamines through the Cu(OAc)2/2-acetylcyclohexanone catalyzed cross-coupling of s-tetrazinylamines with iodofurazans has been developed. The reaction displays good functional group tolerance, involving nitro, azido, and azo groups, which are critical for the construction of energetic materials. Both 3,6-disubstituted and annelated s-tetrazines react readily
    已经开发出通过 Cu(OAc)2/2-乙酰环己酮催化的 s-四嗪基胺与呋咱的交叉偶联获得不对称仲二杂芳胺。该反应显示出良好的官能团耐受性,包括硝基、叠氮基和偶基团,这些基团对于构建含能材料至关重要。3,6-二取代和退火的 s-四嗪都容易与呋喃发生反应以提供所需的产品。
查看更多

同类化合物

酸四嗪 甲四嗪-氨基叔丁酯 四嗪-活性脂 四嗪-氨基叔丁酯 嘧啶并[4,5-e]-1,2,3,4-四嗪 二甲基-1,2,4,5-四嗪 二氯均四嗪 METHYLTETRAZINE-ACID,甲基四嗪-羧基 6-苯基-1,2,4,5-四嗪-3-胺 6-乙基-1,2,4,5-四嗪-3-胺 6-丁基氨基-3-(3,5-二甲基吡唑-1-基)四嗪 6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-胺 3-苯基-6-(吡啶-2-基)-1,2,4,5-四嗪 3,6-二苯基-1,2,4,5-四嗪 3,6-二溴-1,2,4,5-四嗪 3,6-二氨基-1,2-二氢-1,2,4,5-四嗪盐酸盐 3,6-二-4-吡啶基-1,2,4,5-四嗪 3,6-二-2-吡啶基-1,2,4,5-四嗪 3,6-二(噻吩-2-基)-1,2,4,5-四嗪 3,6-二(3-吡啶基)-1,2,4,5-四氮杂苯 3,6-二(3,5-二甲基-1H-吡唑-1-基)-1,2,4,5-四嗪 1-[6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-基]-2-(丙-2-亚基)肼 1,2-二氢-1,2,4,5-四嗪-3,6-二酮 1,2,5-噁二唑-3-胺,4-[(5-甲基-2H-四唑-2-基)甲基]- 1,2,4,5]四嗪-3,6-二羧酸 1,2,4,5-四嗪-3-胺 1,2,4,5-四嗪-3,6-二羧酸二甲酯 1,2,4,5-四嗪,3-甲氧基-6-苯基- 1,2,4,5-四嗪 (9CI)-吡咯并[2,1-d]-1,2,3,5-四嗪 (6-肼基-1,2,4,5-四嗪-3-基)肼 3,6-Dicyclopropyl-s-tetrazin 3-Methyl-4-methylaminotriazol-1-oxid 1,2,4,5-Tetrazin-3-amine, 6-cyclohexyl- 7-amino-2-trifluoromethyl-6-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)-4,4a,5,6-tetra-hydroimidazo[1,5-d][1,3,4]thiadiazin-6-ium pentaiodide 3,6-bis(ethylamino)-1,2,4,5-tetrazine Gtersunqcxeonk-uhfffaoysa- aminotetrazine argon 3-amino-s-tetrazine*Ar2 N-(2-chloro-1-methoxyethyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-amine 3,6-di(2-cyclopentylidenehydrazino)-1,2,4,5-tetrazine 4,4'-(butane-2,3-diylidenebis(azaneylylidene))bis(4H-1,2,4-triazole-3-thiol) 6-Isopropyl-s-triazolo<4,3-b>-s-tetrazin-3-thiol 3-amino-6-(3,5-diamino-1,2,4-triazol-1-yl)-1,2,4,5-tetrazine 3,6-bis(4-bromo-3,5-dimethylpyrazol-1-yl)-1,2,4,5-tetrazine 1,4-s-Tetrazin-15N2 N-(sec-butyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-amine 1,2-Di-4-pyridazinylethanone oxime trans-Pt(S[CN4(C2H5)])2(PMe3)2