CAJ | 학술논문

为合成抗肿瘤药物甲啶铂，采用醋酸铵与K2PtCl4反应生成K[Pt(NH3)Cl3]，再先后与碘化钾、2-甲基吡啶、硝酸银、氯化钾反应生成甲啶铂。采用元素分析、质谱、核磁共振氢谱和红外光谱对其结构进行了表征。结果显示合成的化合物与理论一致，产率约为40%，可为甲啶铂的合成提供一条新的工艺路线。
위합성항종류약물갑정박，채용작산안여K2PtCl4반응생성K[Pt(NH3)Cl3]，재선후여전화갑、2-갑기필정、초산은、록화갑반응생성갑정박。채용원소분석、질보、핵자공진경보화홍외광보대기결구진행료표정。결과현시합성적화합물여이론일치，산솔약위40%，가위갑정박적합성제공일조신적공예로선。
To synthesize a platinum-based anti-tumor drug picoplatin, the key intermediate K[Pt(NH3)Cl3] , synthesized from ammonium acetate and K2PtCl4 was subsequently reacted with KI, 2-picoline, AgNO3 and KCl to give the target compound. The structure and component were characterized by elemental analysis, ESI-MS, 1H-NMR and IR. The results showed that its structure was consistent with the title compound and the yield was about 40%. This provides a new process for the synthesis of picoplatin.