Cyclization of ethyl [cyano(4,6-dimethylpyrimidin-2-yl)amino]-acetate

封面

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Imidazolin-4-one derivatives have been prepared by a reaction of ethyl [cyano(4,6-dimethylpyrimidin-2-yl)amino]acetate (2) with morpholine, piperidine and hydrazides. In the presence of sulfuric acid, cyanoester 2 gives 2-iminooxazolin-5-one which is acylated on the nitrogen atom of imino group and is rearranged to imidzolidin-2,4-dione in the presence of KCNO.

全文:

受限制的访问

作者简介

A. Shiryaev

Samara State Technical University

编辑信件的主要联系方式.
Email: shiryaev.ak@samgtu.ru
ORCID iD: 0000-0001-9165-869X
俄罗斯联邦, ul. Molodogvardeiskaya, 244, Samara, 443100

M. Krasavina

Samara State Technical University

Email: shiryaev.ak@samgtu.ru
ORCID iD: 0009-0003-7753-7500
俄罗斯联邦, ul. Molodogvardeiskaya, 244, Samara, 443100

V. Shiryaev

Samara State Technical University

Email: shiryaev.ak@samgtu.ru
俄罗斯联邦, ul. Molodogvardeiskaya, 244, Samara, 443100

参考

  1. Thakur A., Verma M., Bharti R., Sharma R. Tetrahedron. 2022, 119, 132813. doi: 10.1016/j.tet.2022.132813
  2. Joshi S., Mehra M., Singh R., Kakar S. Egypt. J. Basic Appl. Sci. 2023, 10, 1, 218–239. doi: 10.1080/2314808X.2023.2171578
  3. Kushwaha N., Kushwaha S. Biointerface Res. Appl. Chem. 2022, 12, 5, 6460–6486. doi: 10.33263/BRIAC125.64606486
  4. Rulhania S., Kumar S., Nehra B., Gupta G.D., Monga V. J. Mol. Struct. 2021, 1232, 129982. doi: 10.1016/j.molstruc.2021.129982
  5. Alghamdi S.S., Suliman R.S., Almutairi K., Kahtani K., Aljatli D. Drug Design Develop. Ther. 2021, 15, 3289–3312. doi: 10.2147/DDDT.S307113
  6. Siwach A., Verma P.K. BMC Chem. 2021, 15, 12, 1–69. doi: 10.1186/s13065-020-00730-1
  7. Gujjarappa R., Kabi A.K., Sravani S., Garg A., Vodnala N., Tyagi U., Kaldhi D., Velayutham R., Singh V., Gupta S. Overview on Biological Activities of Imidazole Derivatives. Ed. B.P. Swain. Singapore: Springer. Publ. 2022, 135–227. doi: 10.1007/978-981-16-8399-2_6
  8. Gujjarappa R., Sravani S., Kabi A.K., Garg A., Vodnala N., Tyagi U., Kaldhi D., Singh V., Gupta S., Malakar C.C. An Overview on Biological Activities of Oxazole, Isoxazoles and 1,2,4-Oxadiazoles Derivatives. Ed. B.P. Swain. Singapore: Springer. Publ. 2022, 379–400. doi: 10.1007/978-981-16-8399-2_10
  9. Tolomeu H.V., Fraga C.A.M. Molecules 2023, 28, 838. doi: 10.3390/molecules28020838
  10. Sharma P., LaRosa C., Antwi J., Govindarajan R., Werbovetz K.A. Molecules 2021, 26, 4213. doi: 10.3390/molecules26144213
  11. Guerrero-Pepinosa N.Y., Cardona-Trujillo M.C., Garzґon-Casta˜no S.C., Veloza L.A., Sepúlveda-Arias J.C. Biomed. Pharmacother. 2021, 138, 111495. doi: 10.1016/j.biopha.2021.111495
  12. Albayatia M.R., Mohamed M.F.A., Moustafa A.H. Synth. Commun. 2020, 50, 8, 1217–1231. doi: 10.1080/00397911.2020.1735443
  13. Moustafa A.H., Ahmed W.W., Awad M.F., Aboelez M.O., Khodairy A., Amer A.A. Mol. Div. 2022, 26, 2813–2823. doi: 10.1007/s11030-022-10401-z
  14. Dovlatyan V.V., Eliazyan K.A., Pivazyan V.A. Chem. Heterocycl. Compd. 1994, 30 (9), 1074–1076. doi: 10.1007/BF01171168
  15. Shestakov A.S., Moustafa A.H., Bushmarinov I.S., Goloveshkin A.S., Shapovalov A.V., Shikhaliev K.S., Prezent M.A., Sidorenko O.E. J. Heterocycl. Chem. 2017, 54, 551–560. doi: 10.1002/jhet.2621
  16. Fodor G., Koczka K. J. Chem. Soc. 1952, 850-854. doi: 10.1039/JR9520000850
  17. Dutta S., Higginson C.J., Ho B.T., Rynearson K.D., Dibrov S.M., Hermann T. Org. Lett. 2010, 12 (2), 360–363. doi: 10.1021/ol9026914
  18. Dutta S., Dibrov S.M., Ho B.T., Higginson C.J., Hermann T. J. Chem. Crystallogr. 2012, 42, 119–129. doi: 10.1007/s10870-011-0212-6
  19. Basavaprabhu H., Sureshbabu V.V. Org. Biomol. Chem. 2012, 10 (13), 2528–2533. doi: 10.1039/c2ob06916d
  20. Wildermuth R.E., Steinborn C., Barber D.M., Muhlfenzl K.S., Kendlbacher M., Mayer P., Wurst K., Magauer T. Chem. Eur. J. 2021, 27, 12181–12189. doi: 10.1002/chem.202101849
  21. Steinborn C., Wildermuth R.E., Barber D.M., Magauer T. Angew. Chem. Int. Ed. 2020, 59, 17282–17285. doi: 10.1002/anie.202008158
  22. Masumoto E., Maruoka H., Okabe F., Fujioka T., Yamagata K. J. Heterocycl. Chem. 2015, 52, 48–53. doi: 10.1002/jhet.1946
  23. Birtwell S. J. Chem. Soc. 1953, 1725–1730. doi: 10.1039/JR9530001725

补充文件

附件文件
动作
1. JATS XML
2. Scheme 1. Alkylation of (4,6-dimethylpyrimidin-2-yl)cyanamide (1) with ethyl chloroacetate

下载 (199KB)
3. Scheme 2. Reaction of cyanoester 2 with amines and hydrazides

下载 (524KB)
4. Scheme 3. Cyclization of cyanoester 2 to imidate 6 and reactions of imidate 6

下载 (553KB)
5. Scheme 4. Synthesis of ureas 8a, b from cyanamide 1

下载 (247KB)
6. Scheme 5. Cyclizations of cyanoesters into imidates (TBS – tert-butyldimethylsilyl, PMB – para-methoxybenzyl)

下载 (605KB)
7. Content

下载 (26KB)

版权所有 © Russian Academy of Sciences, 2025