Remennikov, G. Ya.’s team published research in Khimiya Geterotsiklicheskikh Soedinenii in 1983 | CAS: 14001-69-5

2-Methoxy-5-nitropyrimidine(cas: 14001-69-5) is a member of ether. When aromatic ethers are exposed to halogen in the presence or absence of a catalyst, they undergo halogenation, such as bromination.Synthetic Route of C5H5N3O3

Synthetic Route of C5H5N3O3On October 31, 1983 ,《Sigma complexes in the pyrimidine series. 6. Reaction of 5-nitro-2-methoxy- and 5-nitro-4,6-dimethoxypyrimidines with acetylacetone carbanion》 appeared in Khimiya Geterotsiklicheskikh Soedinenii. The author of the article were Remennikov, G. Ya.; Kiselenko, A. A.; Cherkasov, V. M.. The article conveys some information:

Methoxynitropyrimidine I reacted with acetylacetone carbanion to form salt II or acetophenone III, depending on the reaction conditions. Dimethoxynitropyrimidine IV (R = MeO) was not converted to salt V by this reaction; V could be obtained from IV [R = (MeCO)2CH]. The conversion of acetonylpyrimidine VI to salt VII was also described. The results came from multiple reactions, including the reaction of 2-Methoxy-5-nitropyrimidine(cas: 14001-69-5Synthetic Route of C5H5N3O3)

2-Methoxy-5-nitropyrimidine(cas: 14001-69-5) is a member of ether. When aromatic ethers are exposed to halogen in the presence or absence of a catalyst, they undergo halogenation, such as bromination.Synthetic Route of C5H5N3O3

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia