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1-(2-噻吩基)-2-丙胺

维基百科,自由的百科全书
(重定向自噻吩丙胺
1-(2-噻吩基)-2-丙胺
臨床資料
其他名稱Thiophenylpropylamine; 1-Methyl-2-thiophen-2-yl-ethylamine; 2-(2-Aminopropyl)thiophene; 1-(2-Thienyl)-2-aminopropane
法律規範狀態
法律規範
识别信息
  • 1-(thiophen-2-yl)-2-aminopropane
CAS号30433-93-3  checkY
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
化学信息
化学式C7H11NS
摩尔质量141.23 g·mol−1
3D模型(JSmol英语JSmol
  • CC(N)Cc1sccc1
  • InChI=1S/C7H11NS/c1-6(8)5-7-3-2-4-9-7/h2-4,6H,5,8H2,1H3 checkY
  • Key:NYVQQTOGYLBBDQ-UHFFFAOYSA-N checkY

1-(2-噻吩基)-2-丙胺,简称噻吩丙胺,是一种有机化合物,化学式为C7H11NS,它是一种兴奋剂。它可由2-(2-硝基-1-丙烯-1-基)噻吩经氢化铝锂还原[3],或1-(2-噻吩基)-2-丙酮和钛酸四异丙酯催化下反应,经硼氢化钠还原得到[4]。它和异硫氰酸甲酯反应,可以得到N-甲基-N'-[1-甲基-2-(2-噻吩基)乙基]硫脲。[3]

参考文献

[编辑]
  1. ^ STATUS DECISION OF CONTROLLED AND NON-CONTROLLED SUBSTANCE(S) (pdf). Health Canada. 2013-07-31. [2025-02-28].
  2. ^ 国家禁毒办决定将尼秦类物质和12种新精神活性物质纳入管制. 人民网. 2025-06-19 [2025-06-19]. 
  3. ^ 3.0 3.1 Foye, William O.; et al. Heterocyclic analogs of amphetamine: thioureas, dithiocarbamates, and negatively substituted amides. Journal of Pharmaceutical Sciences (1979), 68(5), 591-595.
  4. ^ Albarran-Velo, Jesus; et al. Markovnikov Wacker-Tsuji Oxidation of Allyl(hetero)arenes and Application in a One-Pot Photo-Metal-Biocatalytic Approach to Enantioenriched Amines and Alcohols. Advanced Synthesis & Catalysis (2021), 363(16), 4096-4108. doi:10.1002/adsc.202100351.