Unexpected Reaction Products of Uracil and Its Methyl Derivatives with Acetic Anhydride and Methylene Chloride

التفاصيل البيبلوغرافية
العنوان: Unexpected Reaction Products of Uracil and Its Methyl Derivatives with Acetic Anhydride and Methylene Chloride
المؤلفون: Slawomir Filipek, Olga Michalak, Przemyslaw Miszta, Kinga Trzcińska, Piotr Krzeczyński, Piotr Cmoch, Marcin Cybulski, Pakhuri Mehta, Andrzej Leś
المصدر: The Journal of Organic Chemistry. 86:14321-14332
بيانات النشر: American Chemical Society (ACS), 2021.
سنة النشر: 2021
مصطلحات موضوعية: Methylene Chloride, Organic Chemistry, Acetic Anhydrides, Substituent, Uracil, Mass spectrometry, Chloride, Medicinal chemistry, Thymine, chemistry.chemical_compound, Acetic anhydride, chemistry, medicine, Moiety, Methylene, medicine.drug
الوصف: New acetyl derivatives of uracil, 6-methyluracil, and thymine were obtained in the course of an unconventional synthesis in methylene chloride. It was shown that products with the acetyloxymethyl fragment are formed according to a mechanism different from that for products with the acetyloxyethyl group. In particular, for uracil it was proven that the reaction with Ac2O, TEA, and CH2Cl2 leads to 1-acetyloxymethyluracil, where the N1 substituent is composed of the -CH2- fragment that originated from CH2Cl2 and the 1-acetyloxy moiety from Ac2O. The reaction of uracil with Ac2O, TEA, CH2Cl2, and DMAP leads to an acetyloxyethyl derivative in which the -CH2-CH2- fragment originates from TEA and the 1-acetyloxy moiety from Ac2O. A possible mechanism for the formation of new compounds was suggested and supported by the density functional theory/B3LYP quantum mechanical calculations. New compounds (39 in total, including seven deuterated) were fully characterized by nuclear magnetic resonance and high-resolution mass spectrometry techniques.
تدمد: 1520-6904
0022-3263
DOI: 10.1021/acs.joc.1c00748
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8979c26496d18df385d9f1e912ce634e
https://doi.org/10.1021/acs.joc.1c00748
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....8979c26496d18df385d9f1e912ce634e
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15206904
00223263
DOI:10.1021/acs.joc.1c00748