Synthesis of pyrimidines from dinitrogen and carbon

Author:

Shi Xianghui1,Wang Qianru2,Qin Chao2,Wu Li-Jun1,Chen Yuanjin1,Wang Gao-Xiang1,Cai Yongli23,Gao Wenbo23,He Teng23,Wei Junnian1,Guo Jianping23,Chen Ping234,Xi Zhenfeng1ORCID

Affiliation:

1. Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University , Beijing 100871 , China

2. Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023 , China

3. University of Chinese Academy of Sciences , Beijing 100049 , China

4. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023 , China

Abstract

Abstract The element nitrogen and nitrogenous compounds are vital to life. The synthesis of nitrogen-containing compounds using dinitrogen as the nitrogen source, not through ammonia, is of great interest and great value but remains a grand challenge. Herein, we describe a strategy to realize this transformation by combining the heterogeneous approach with the homogeneous methodology. The N2 molecule was first fixed with carbon and LiH through a one-pot heterogeneous process, forming Li2CN2 as an ‘activated’ nitrogen source with high efficiency. Then subsequent homogeneous treatments of Li2CN2 to construct the organic synthon carbodiimide and the RNA/DNA building block pyrimidines were fulfilled. By using 15N2 as the feedstock, their corresponding 15N-labeled carbodiimide and pyrimidines were readily obtained. This homogeneous–heterogeneous synergy strategy will open a new chapter for N2 transformation.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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