Rhodium-Catalyzed Regioselective Direct C-H Amidation of 2,4-Diarylquinazoline with Sulfonyl Azides: An Example of Steric Hindrance Regulated Mono- and Diamidation Selectivity

被引:38
|
作者
Zhang, Chunyan [1 ]
Zhou, Yirong [1 ]
Deng, Zhihong [1 ]
Chen, Xin [1 ]
Peng, Yiyuan [1 ]
机构
[1] Jiangxi Normal Univ, Coll Chem, Key Lab Green Chem, Key Lab Small Fuct Organ Mol,Minist Educ, Nanchang 330022, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Synthetic methods; C-H activation; Nitrogen heterocycles; Regioselectivity; Rhodium; Sulfonamides; ONE-POT SYNTHESIS; INTERMOLECULAR AMIDATION; CONVENIENT SYNTHESIS; CASCADE SYNTHESIS; DIRECT AMINATION; BOND ACTIVATION; DUAL AMINATION; ARENES; QUINAZOLINE; ACCESS;
D O I
10.1002/ejoc.201403477
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An unprecedented steric hindrance controlled regioselective rhodium-catalyzed direct C-H amidation of 2,4-diarylquinazoline was described. Sulfonyl azides were used as the amine source to provide a variety of amide-functionalized 2,4-diarylquinazolines in high efficiency. The reaction proceeded under mild conditions, had good functional group tolerance with a broad scope of substrates, and afforded moderate to good product yields. Excellent monoamidation selectivity was achieved with the assistance of meta substituents.
引用
收藏
页码:1735 / 1744
页数:10
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