An unprecedented tandem synthesis of fluorescent coumarin-fused pyrimidines via copper-catalyzed cross-dehydrogenative C(sp3)-N bond coupling

被引:14
作者
Kumari, Santosh [1 ]
Shakoor, S. M. Abdul [1 ]
Khullar, Sadhika [2 ]
Mandal, Sanjay K. [3 ]
Sakhuja, Rajeev [1 ]
机构
[1] Birla Inst Technol & Sci, Dept Chem, Pilani 333031, Rajasthan, India
[2] DAV Univ, Dept Chem, Jalandhar 144012, Punjab, India
[3] Indian Inst Sci Educ & Res Mohali, Dept Chem Sci, Sect 81,Manuali PO, Sas Nagar 140306, Punjab, India
关键词
C-H ACTIVATION; TERTIARY-AMINES; FLEMINGIA-CHAPPAR; ACCESS; FUNCTIONALIZATION; HETEROCYCLES; STRATEGY; DERIVATIVES; CYCLIZATION; AMIDATION;
D O I
10.1039/c8ob00586a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient, one-pot Cu-catalyzed tandem synthesis of fluorescent 1-benzyl-2-phenyl-1,2-dihydro-5H-chromeno[4,3-d]pyrimidin-5-ones from 4-chloro-3-formylcoumarin and benzylamines was developed by in situ intramolecular cross-dehydrogenative C(sp(3))-N bond formation in moderate-to-good yields under ligand-free ambient conditions. This synthesis was easily scalable, and the generality of the substrates was established. These coumarin-fused pyrimidines exhibited interesting photo-physical properties and high quantum yields, and would be potential candidates for facilitating suitable studies in medicinal chemistry and materials science.
引用
收藏
页码:3220 / 3228
页数:9
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