Alkenyl derivatives of 5-nitro-2-pyridone: Synthesis and halocyclization


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Alkylation of 5-nitro-2-pyridone by alkenyl halides in acetone in the presence of K2СО3 proceeds with generation of a mixture of N- and О-derivatives with N-isomer prevailing. 1-Allyl- and 1-methylallyl-5-nitro-2-pyridone react with halogens with the formation of 2-halomethyl-6-nitro-2,3-dihydrooxazolo[3,2-a]-pyridinium halides. 1-Prenyl-5-nitro-2-pyridone reacts with bromine with the formation of 3-bromine-2,2-dimethyl-7-nitro-3,4-dihydro-2Н-pyrido[2,1-b][1,3]oxazinium bromide, and with iodine giving 2,2-dimethyl-7-nitro-3,4-dihydro-2Н-pyrido[2,1-b][1,3]oxazinium triiodide.

作者简介

E. Kalita

South Ural State University (National Research University)

编辑信件的主要联系方式.
Email: berdnik_lena@mail.ru
俄罗斯联邦, pr. Lenina 76, Chelyabinsk, 454080

D. Kim

South Ural State University (National Research University)

Email: berdnik_lena@mail.ru
俄罗斯联邦, pr. Lenina 76, Chelyabinsk, 454080

O. Yeltsov

Ural Federal University

Email: berdnik_lena@mail.ru
俄罗斯联邦, Yekaterinburg

T. Shtukina

Ural Federal University

Email: berdnik_lena@mail.ru
俄罗斯联邦, Yekaterinburg

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