Synthesis of aza-aromatic hydroxylamine-O-sulfonates and their application to tandem nucleophilic addition–electrophilic 5-endo-trig cyclization
作者:Jaroslaw Saczewski、Maria Gdaniec、Patrick J. Bednarski、Anna Makowska
DOI:10.1016/j.tet.2011.03.091
日期:2011.5
investigated with use of the long-range corrected hybrid density functional ωB97X-D/6-31+G∗ and SM8 (DMF) solvation model. The structures of the heteroaromatic hydroxylamine-O-sulfonates and N-(5-methoxy-2H-[1,2,4]thiadiazolo[2,3-a]pyrimidin-2-ylidene)benzamide were confirmed by single crystal X-ray analysis. N-(2H-[1,2,4]thiadiazolo[3,2-a]isoquinolin-2-ylidene)benzamide exhibited a pronounced in vitro cytostatic
羟胺-O-磺酸(HOSA)被用作2-氯嘧啶,2-氯喹啉和1-氯异喹啉的有效亲核胺化试剂。新获得的杂芳族羟胺Ò -sulfonates经受与酰基反应异硫氰酸酯后行串联亲核加成亲电5-内切- TRIG环化。使用远程校正的杂化密度泛函ωB97X-D/ 6-31 + G ∗和SM8(DMF)溶剂化模型研究了环化的机理。杂芳族羟胺-O-磺酸盐和N-(5-甲氧基-2 H- [1,2,4]噻二唑[2,3- a ]的结构通过单晶X射线分析确认了[嘧啶-2-亚苄基]苯甲酰胺。N-(2 H- [1,2,4]噻二唑[3,2 - a ]异喹啉-2-亚基)苯甲酰胺对人肿瘤细胞系SISO,LCLC,A-427,DAN- G和RT-4(IC 50范围为1.47-2.97μM)。