2-(3,3-二苯基丙基)咪唑-5-乙胺
化合物
2-(3,3-二苯基丙基)咪唑-5-乙胺一類強效且具有選擇性的組胺H1受體激動劑的母體化合物[1],化學式為C20H23N3,它可以二苯甲烷為原料,經多步反應製得。[2]
2-(3,3-二苯基丙基)咪唑-5-乙胺 | |
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別名 | 二苯丙基組胺(Histaprodifen) 2-(3,3-二苯基丙基)組胺 |
識別 | |
CAS號 | 222545-59-7 |
SMILES |
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性質 | |
化學式 | C20H23N3 |
摩爾質量 | 305.42 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
它和4-吡啶乙酸鹽酸鹽在吡啶和CDI的存在下於THF中反應,可以得到N-[2-(3,3-二苯基丙基)咪唑-5-基乙基]-4-吡啶乙醯胺。[3]
參考文獻
- ^ Sigurd Elz, Kai Kramer, Christian Leschke, Walter Schunack. Ring-substituted histaprodifen analogues as partial agonists for histamine H1 receptors: synthesis and structure–activity relationships. European Journal of Medicinal Chemistry, 2000. 35 (1): 41-52. doi:10.1016/S0223-5234(00)00105-7.
- ^ Elz S, Kramer K, Pertz HH; et al. Histaprodifens: synthesis, pharmacological in vitro evaluation, and molecular modeling of a new class of highly active and selective histamine H1-receptor agonists. J. Med. Chem. 2000, 43 (6): 1071–1084. PMID 10737740.
- ^ Sonja Menghin, Heinz H. Pertz, Kai Kramer, Roland Seifert, Walter Schunack, and Sigurd Elz. Nα-Imidazolylalkyl and Pyridylalkyl Derivatives of Histaprodifen: Synthesis and in Vitro Evaluation of Highly Potent Histamine H1-Receptor Agonists. J. Med. Chem. 2003, 46, 25, 5458–5470. doi:10.1021/jm0309147.