📜4-氯羰酰四氢-吡啶羧酸苄酯置于sodium Azide体系中,用 丙酮,甲苯 用作溶剂,化学反应生成4-异硫氰四羟基-1(2H)-吡啶甲酸苄酯
参考文献:Antagonists Of The Human Ccr5 Receptor As Anti-Hiv-1 Agents. Part 4: Synthesis And Structure-activity Relationships For 1-[n-(Methyl)-N-(Phenylsulfonyl)Amino]-2-(Phenyl)-4-(4-(N-(Alkyl)-N-(Benzyloxycarbonyl)Amino)Piperidin-1-yl)Butanes
标题:Antagonists Of The Human Ccr5 Receptor As Anti-Hiv-1 Agents. Part 4: Synthesis And Structure-activity Relationships For 1-[n-(Methyl)-N-(Phenylsulfonyl)Amino]-2-(Phenyl)-4-(4-(N-(Alkyl)-N-(Benzyloxycarbonyl)Amino)Piperidin-1-yl)Butanes
摘要:(2S)-2-(3-氯苯基)-1-[n-(甲基)-N-(苯磺酰基)氨基]-4-[螺环(2,3-二氢苯并噻吩-3,4'-哌啶-1'-基)]丁烷 S-氧化物 (Lb) 已被鉴定为一种强效的 Ccr5 拮抗剂,其 Ic50 = 10 Nm.在此,描述了非螺环哌啶的结构-活性关系研究,这些研究导致了发现 4-(N-(烷基)-N-(苯甲酰氧基)氨基)哌啶衍生物 (3-5) 作为强效的 Ccr5 拮抗剂.(C) 2001 Elsevier Science Ltd. 保留所有权利.
Doi:10.1016/s0960-894X(01)00492-9