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Metal free [4+1] and [5+1] annulation reactions to prepare heterocycles using DMF and its derivatives as one-carbon source
被引:12
|作者:
Xu, Yiwen
[1
]
Shen, Bei
[1
]
Liu, Lingfeng
[1
]
Qiao, Chunhua
[1
]
机构:
[1] Soochow Univ, Coll Pharmaceut Sci, Suzhou 215123, Peoples R China
关键词:
Annulation reaction;
DMF;
1,2,4-triazolo[3,4-a]pyridine;
Triazine;
RECEPTOR ANTAGONISTS;
CATALYZED SYNTHESIS;
POTENT;
TRIAZOLOPYRIDINES;
GUANAMINES;
INHIBITOR;
KINASE;
D O I:
10.1016/j.tetlet.2020.151844
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
1,2,4-Triazolo[3,4-a]pyridines and related heterocycles and substituted triazines were commonly discovered scaffolds in a variety of pharmaceutical and agrochemical agents. Herein, we report a highly efficient and practical method using DMF and its derivative for the [4+1] and [5+1] annulation reactions to prepare these heterocycles. This metal free reaction takes advantages of shelf stable DMF as solvent and carbon donor, imidazole chloride as a catalyst, the mild reaction condition tolerates a broad substrate range and substitutes. The prepared 3-unsubstituted 1,2,4-triazolo[3,4-a]pyridine and derivatives allow further introduction of a variety of functional group1 at 3-position. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:6
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