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【结 构 式】

【药物名称】

【化学名称】N,N',N'',N'''-(1,4,8,11-Tetraazacyclotetradecan-1,4,8,11-tetrayl)tetrakis(pentane-1,5-diyl)tetrakis(N-benzylcarbamic acid tert-butyl ester)

【CA登记号】192518-27-7

【 分 子 式 】C78H124N8O8

【 分 子 量 】1301.90678

【开发单位】INSERM (Originator)

【药理作用】AIDS Medicines, Anti-HIV Agents, ANTIINFECTIVE THERAPY

合成路线1

The title compound was obtained by alkylation of tetraazacyclo tetradecane (I) with an excess of tosylate (II) in the presence of K2CO3 in refluxing acetonitrile.

1 Trabaud, C.; Dessolin, J.; Camplo, M.; Hantz, O.; Zoulim, F.; Borel, C.; Meyer, M.; Pepe, G.; Chermann, J.-C.; Kraus, J.-L.; Design, synthesis and structure relationships of new N,N',N'',N'''-tetrakis (omega-amino alkyl) tetraazamacrocycles. Antivir Chem Chemother 1998, 9, 1, 73-84.
2 Chermann, J.C.; Dessolin, J.; Bouygues, M.; Trabaud, C.; Kraus, J.L.; Vieghe, P.; Camplo, M.; Modelisation, synthesis and anti-HIV activities of N,N,N',N'',N'''-pentakistetraazamacrocycles salts derivatives. Bioorg Med Chem Lett 1997, 7, 10, 1353.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 25362 1,4,8,11-Tetraazacyclotetradecane 295-37-4 C10H24N4 详情 详情
(II) 28072 5-[benzyl(tert-butoxycarbonyl)amino]pentyl 4-methylbenzenesulfonate C24H33NO5S 详情 详情
Extended Information