MALЕIN ANGIDRIDNING BЕNZIDIN VA 1,2-ETANDIOL BIS (4-AMINOBENZOAT) BILAN RЕAKSIYALARI

Main Article Content

Turayeva Xurshida Kamalbayevna

Аннотация:

Malein angidridni diaminlardan benzidin va 1,2-etandiol bis (4-aminobenzoat) bilan olib borilgan reaksiyalari asosida malein kislotaning monoamidli, bis-amidli va bis-maleinimidli, izo-maleinimidli birikmalarini olishning qulay usullarini topish ustida ilmiy izlanishlar olib borildi, reaksiya sharoitlarini tahlillari o'rganildi. Aniqlangan va taklif qilingan usullar orqali reaksiyaning borishida erituvchi va haroratning ta'siri ma'lum misollari va qonuniyatlar asosida tahlil qilindi. Olingan birikmalarning tozaligi yupqa qatlam (YuQX) va gaz suyuqlik xromatografiyalari (GSX), shuningdek, tuzilishi IQ-spektroskopiya, xromato-mass-spektrometriya usullar yordamida isbotlangan, shuningdek, spektr tahlillari muhokamasi orqali tasdiqlangan.

Article Details

Библиографические ссылки:

F. Yongxian, Lu. Yuele et al. “Anti-Leishmanial and Cytotoxic Activities of a Series of Maleimides”, (Molecules, MDPI, 2018), p.2878

Курапова М. Ю. Жакина А.Х. и др. Синтез новых сукцинимидных производных на основе этилового эфира п-аминобензойной кислотоы. // Cерия химическая. 2008. –№ 6. –С.43-44

M. A. Ahlam and S. A. Rhahman Mahdi, “Synthesis and Evaluation of Antimicrobial activity of several new Maleimides to Benzothiazole moiety” , (Baghdad Science Journal, Baghdad, 2013), р.658

A. Yu. Simonov, S. A. Lakatosh et al. “Nucleophilic substitution and cyclization reactions involving quaternized 3-dimethylaminomethyl derivatives of 3,4-bis (indol-1-yl) maleimide and 3- (indol-1-yl) -4- (indolin-1yl) maleimide”, (Izvestiya AN. Ser. chem., Russian, 2010), pp.1409-1417

Ahn Hyung Kaok, C.Gasmon Robert et al. “Dentistry adhesive”, U.S. Patent No. 6166102 (2002).

D. Jain, J. Maheshwari et al. “Synthesis and free radical polymerization of n[4-fluoro phenyl] maleimide and study of properties of polymers”, (Rasayan J.Chem, India, 2012), рр.445-449

O. A. Kolyamshin, V. A. Danilov et al. “Synthesis of new bis-maleimides based on alkylaromatic diamines”, (Bulletin of Kazan Technological University, Kazan, 2011), pp.46-48.

J. Chaudhary, S. Purohit et al. “Synthesis and characterization of maleimide-epoxy resins and composites formation”, (Der Pharma Chemica, United States, 2017), pp.1-4

K. F. Lin, J. S. Lin et al. “High temperature resins based on allylamine/bismaleimides”, (Polymer, MDPI, 1996), pp.4729–4737.

"Lockheed Martin F-35B Boasts UFO Technology, Fights For Team USA". International Science Time s. August 21, 2013. Retrieved 28 January 2014.

Hair spray. (Soap and Cosmet. 2001. V. 77. № 11. С. 54. Аngl. 2002), p.56.

J. S. Stetter, Hans-Joachim et al. “N-Arylpyrrolin-2,5-dione ", U.S. Patent No. 3712987 (10 November 1988)

E. B. Donald. “N-(trifluoromethyl- and trifluoromethylhalophenyl)-maleimides”, U.S. Patent No. 3850955 (26 Novomber 1974)

O. Yoshitosi, K. Tohru et al. “New insecticidal esters of cyclopropanedicarboxylic acid”, U.S. Patent No. 938 (12 January 1973)

Васильева С. Ю. Журавлева Н. В. Колямшин О. А. и др. Изучение кинетических закономерностей реакций синтеза и свойств малеинимидов // Вестник Чувашского университета. – 2011. – №. 3. – С. 204-209.

J. K. Weltman, R. P. Szaro et al. “N-(3-pyrene)maleimide: a long lifetime fluorescent sulfhydryl reagent”, (The Journal of Biological Chemistry, United States 1973), pp. 3173-3177.

Колямшин О. А., Данилов В. А., Кольцов Н. И. Эфиры 4-(3-диалкиламино-2, 5-диоксо-2, 3, 4, 5-тетрагидро-1H-пирролил) бензойной кислоты // ЖОрХ. – 2007. – Т. 43. – №. 3. – С. 395-397.

Коляшин О.А., Данилов В.А., Дашкова Г.Ю., Кольцов Н.А. Эфиры 4-(3-диалкиламино-2,5-диоксо-2,3,4,5-тетрагидро-1Н-пирролил) фенил-уксусной кислоты. // ЖОрХ. 2005. –Т. 41. –Вып. 11. –С.1691-1694.

Колямшин О. А., Васильева С. Ю., Кольцов Н. И. Синтез N-бутоксифенилмалеимидов //Журнал органической химии. – 2001. – Т. 37. – №. 11. – С. 1687-1688.

E. Philipp and R. Helmut “Microwave-assisted synthesis, transesterification and polymerization of N-(2-acetoxy-ethyl-)maleimide”, (Designed Monomers and Polymers, Netherlands, 2005), pp.601–607

C. Hulubei and S. Morariu “Synthesis and radical polymerization of N-(3-acetyl-4-carboxy-phenyl)-maleimide”, (High Perform. Polym, United Kingdom, 2000), pр.525–533.

K. N. Shivananda and N. M. Kadidal. “Preparation and curing studiesof maleimide bisphenol–а based epoxy resins”, (Bull. Korean Chem.Soc. Weinheim, 2006), pp.1542-1548.

V. A. Danilov (dis. abstract. cand. chem. sciences. Kazan, 2013), Pp.6-7

N. R. Conley, R. J. Hung et al. “A new synthetic route to authentic N-substituted aminomaleimides”, (J. Org. Chem. Russia, 2005), pp. 4553-4555.

C. C. Randell, K. D. Turnbull “Synthesis on N-alkylated maleimides”, (Synth. Commun. United States, 2000), pр.1379-1388.

F. G. Mizori, S. M. Dershem. U.S. Patent No. 5973166A. (26 Octomber 1999)

T. Engel, G. Kickelbick. “Thermoreversible reactions on inorganic nanoparticle surfaces: Diels-Alder reactions on sterically crowded surfaces”, (Chemistry of Materials, 2013), pp.149-157.

R. C. Clevenger, K. D. Turnbull. “Synthesis on N-alkylated maleimides”, (Synth. Commun. United States, 2000), pp.1379-1388.

K. Julia, D. H. Martin et al. “Tuning the self-healing behavior of one-component intrinsic polymers”, (Polymer, MDPI, 2015), pp.321-329.

R. D. Sunita and P. M. Shailaja “A facile syunthesis of N-substituted maleimides”, (Indian Journal of Chemistry, Indian, 2010), pp.487-488

Rubinstein H., Skarbek J. E., Fever H. Reactions of 3-carboxyacryloylhydrazines and the formation of meleimides, isomaleimides, and pyridazinones // J.Org.Chem.– 1971. – V. 36. – №. 22. – P. 3372-3376.

Hiran B. L., Paliwal S. N. et al. Synthesis, Characterization and Copolymerization of N-(phenylamino) maleimide with MMA // Journal of Chemistry. – 2007. – V. 4. – №. 2. – P. 265-271.

Hergenrother P. M., Connell J. W., Havens S. J. N-(3-ethynylphenyl) maleimide: пат. 4937356 США. – 1990.

Шульц Э. Э., Шакиров М. М., Толстиков Г. А. и др. Аддукты тебаина с малеинимидами. Синтез и превращения // ЖОрХ. – 2005. – Т. 41. – №. 8. – С. 1155-1166.

Matuszak N. Muccioli, G. G., Labar, G. et al. Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors // J. Med. Chem. – 2009. – V. 52. – №. 23. – P. 7410-7420.

Walker M. A. A high yielding synthesis of N-alkyl maleimides using a novel modification of the Mitsunobu reaction // J. Org. Chem. – 1995. – V. 60. – №. 16. – P. 5352-5355. https://doi.org/10.1021/jo00121a070

Cotter R. J., Sauers C. K., Whelan J. M. The synthesis of N-substituted isomaleimides // J. Org. Chem.. – 1961. – V. 26. – №. 1. – P. 10-15.

Isobe T., Ishikawa T. 2-Chloro-1, 3-dimethylimidazolinium chloride. 2. Its application to the construction of heterocycles through dehydration reactions // J. Org. Chem. – 1999. – V. 64. – №. 19. –P. 6989-6992.

Haval K. P., Mhaske S. B., Argade N. P. Cyanuric chloride: decent dehydrating agent for an exclusive and efficient synthesis of kinetically controlled isomaleimides //Tetrahedron. – 2006. – V. 62. – №. 5. – P. 937-942.

Klimenkovs I., Bakis E., Priksane A. Propanephosphonic Acid Anhydride–Mediated Cyclodehydration of Maleic Acid Monoamides //Synthetic Communications. – 2013. – V. 43. – №. 19. – P. 2634-2640.

Klimenkovs I. et al. Maleic diamide polymerizable surfactants. Applications in emulsion polymerization //Comptes Rendus Chimie. – 2003. – V. 6. – №. 11-12. – P. 1295-1304. https://doi.org/10.1016/j.crci.2003.07.015

Тураева Х. К., Юлдашева М. Р. Малеин ангидридни бензидин билан реакцияси // “Аналитик кимё фанининг долзарб муаммолари” VI Респ. илмий-амалий анжумани. Термиз. 2020. 206 б.

Kh. К. Turaeva, M. К. Yuldasheva et al. “Synthesis of meta-altered arylmaleinamide and preparation of esters in their presence”, (Chemistry and chemical engineering, Tashkent, 2020), pp. 30-38.