Pyrrolo[2,3-d]pyrimidine derivatives in the synthesis of a novel heterocyclic system 2a,5a,7-triazaacenaphthylene

被引:1
作者
Muzychka, Lyubov V. [1 ]
Yaremchuk, Iryna O. [1 ]
Verves, Evgenii V. [1 ]
Smolii, Oleg B. [1 ]
机构
[1] Natl Acad Sci Ukraine, VP Kukhar Inst Bioorgan Chem & Petrochem, 1 Murmanska St, UA-02094 Kiev, Ukraine
关键词
pyrimido[5'; 4':4; 5]pyrrolo[2; 1-c][1; 4]oxazine; pyrrolo[2; 3-d]pyrimidine; 2a; 5a; 7-triazaacenaphthylene; cyclization; iodination; INHIBITOR; POTENT;
D O I
10.1007/s10593-019-02471-z
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A convenient method for the synthesis of methyl 8-oxo-3H,8H-2a,5a,7-triazaacenaphthylene-2-carboxylate by iodination of 7-allyl-4-methoxypyrrolo[2,3-d]pyrimidine-6-carboxylic acid methyl ester followed by elimination of hydrogen iodide has been developed. The use of 4-methoxypyrrolo[2,3-d]pyrimidine-6-carboxylic acid as the starting compound led to the formation of iodomethylpyrimido[5',4':4,5]-pyrrolo[2,1-c][1,4]oxazine, a promising precursor for the synthesis of a new tricyclic system based on pyrrolo[2,3-d]pyrimidine.
引用
收藏
页码:397 / 400
页数:4
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