Synthesis of 4-aryl-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d]pyrimidines by a combination of the Suzuki cross-coupling and N-arylation reactions

被引:32
作者
Dodonova, Jelena [1 ]
Skardziute, Lina [2 ]
Kazlauskas, Karolis [2 ]
Jursenas, Saulius [2 ]
Tumkevicius, Sigitas [1 ]
机构
[1] Vilnius Univ, Dept Organ Chem, LT-03225 Vilnius, Lithuania
[2] Vilnius Univ, Inst Appl Res, LT-10222 Vilnius, Lithuania
关键词
Pyrrolo[2,3-d]pyrimidines; Suzuki reaction; N-Arylation; Oligoarylenes; Fluorescence; HALOGENATED NITROGEN; KINASE INHIBITORS; POTENT INHIBITORS; SUBSTITUENTS; PYRIMIDINES; DERIVATIVES; OLIGOMERS; MOLECULE; CATALYST; DEVICES;
D O I
10.1016/j.tet.2011.10.040
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A simple and facile synthesis of novel 4-aryl-2-chloro-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d]pyrimidines with various aryl and heteroaryl assemblies in the heterocyclic framework by a combination of Suzuki cross-coupling and N-arylation reactions of 2,4-dichloropyrrolo[2,3-d]pyrimidine with arylboronic acids and haloarenes are described. A majority of the synthesized compounds were found to emit in a near UV-blue spectral range with fluorescence quantum yields up to 67%. The impact of aryl groups attached to the pyrrole ring of pyrrolopyrimidine derivatives on optical properties is discussed. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:329 / 339
页数:11
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