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Functional Derivatives of 4-Formyl-2-methoxyphenyl Pyridine-4-carboxylate
Acylation of vanillin with isonicotinoyl chloride gave 4-formyl-2-methoxyphenyl pyridine-4-carboxylate which was converted into a number of functional derivatives, including those containing isoxazole and isothiazole heterocycles. In particular, the condensation of the title compound with primary am...
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Published in: | Russian journal of organic chemistry 2019-10, Vol.55 (10), p.1483-1494 |
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container_end_page | 1494 |
container_issue | 10 |
container_start_page | 1483 |
container_title | Russian journal of organic chemistry |
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creator | Potkin, V. I. Bumagin, N. A. Dikusar, E. A. Petkevich, S. K. Kurman, P. V. |
description | Acylation of vanillin with isonicotinoyl chloride gave 4-formyl-2-methoxyphenyl pyridine-4-carboxylate which was converted into a number of functional derivatives, including those containing isoxazole and isothiazole heterocycles. In particular, the condensation of the title compound with primary amines afforded the corresponding Schiff bases. 4-Formyl-2-methoxyphenyl pyridine-4-carboxylate and one of the Schiff bases derived therefrom were reduced with sodium triacetoxohydridoborate to the corresponding alcohol and amine which were acylated with 5-arylisoxazole- and 4,5-dichloroisothiazole-3-carbonyl chlorides to obtain esters and amides having isoxazole and isothiazole fragments. The synthesized compounds readily formed complexes with palladium(II) chloride, which showed a high catalytic activity in the Suzuki reaction of 3-bromobenzoic acid with 4-methoxyphenylboronic acid in water in the absence of an organic solvent. |
doi_str_mv | 10.1134/S1070428019100063 |
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I. ; Bumagin, N. A. ; Dikusar, E. A. ; Petkevich, S. K. ; Kurman, P. V.</creator><creatorcontrib>Potkin, V. I. ; Bumagin, N. A. ; Dikusar, E. A. ; Petkevich, S. K. ; Kurman, P. V.</creatorcontrib><description>Acylation of vanillin with isonicotinoyl chloride gave 4-formyl-2-methoxyphenyl pyridine-4-carboxylate which was converted into a number of functional derivatives, including those containing isoxazole and isothiazole heterocycles. In particular, the condensation of the title compound with primary amines afforded the corresponding Schiff bases. 4-Formyl-2-methoxyphenyl pyridine-4-carboxylate and one of the Schiff bases derived therefrom were reduced with sodium triacetoxohydridoborate to the corresponding alcohol and amine which were acylated with 5-arylisoxazole- and 4,5-dichloroisothiazole-3-carbonyl chlorides to obtain esters and amides having isoxazole and isothiazole fragments. The synthesized compounds readily formed complexes with palladium(II) chloride, which showed a high catalytic activity in the Suzuki reaction of 3-bromobenzoic acid with 4-methoxyphenylboronic acid in water in the absence of an organic solvent.</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S1070428019100063</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Acylation ; Amides ; Amines ; Carbonyls ; Catalytic activity ; Chemical reactions ; Chemistry ; Chemistry and Materials Science ; Chlorides ; Derivatives ; Esters ; Imines ; Organic Chemistry ; Palladium ; Phosgene ; Vanillin</subject><ispartof>Russian journal of organic chemistry, 2019-10, Vol.55 (10), p.1483-1494</ispartof><rights>Pleiades Publishing, Ltd. 2019</rights><rights>Copyright Springer Nature B.V. 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-8cf57aa1edd330a0c0577dcc4841e0717d8aaae048ffed3030c36bd2cd22bfb73</citedby><cites>FETCH-LOGICAL-c316t-8cf57aa1edd330a0c0577dcc4841e0717d8aaae048ffed3030c36bd2cd22bfb73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Potkin, V. 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In particular, the condensation of the title compound with primary amines afforded the corresponding Schiff bases. 4-Formyl-2-methoxyphenyl pyridine-4-carboxylate and one of the Schiff bases derived therefrom were reduced with sodium triacetoxohydridoborate to the corresponding alcohol and amine which were acylated with 5-arylisoxazole- and 4,5-dichloroisothiazole-3-carbonyl chlorides to obtain esters and amides having isoxazole and isothiazole fragments. The synthesized compounds readily formed complexes with palladium(II) chloride, which showed a high catalytic activity in the Suzuki reaction of 3-bromobenzoic acid with 4-methoxyphenylboronic acid in water in the absence of an organic solvent.</description><subject>Acylation</subject><subject>Amides</subject><subject>Amines</subject><subject>Carbonyls</subject><subject>Catalytic activity</subject><subject>Chemical reactions</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chlorides</subject><subject>Derivatives</subject><subject>Esters</subject><subject>Imines</subject><subject>Organic Chemistry</subject><subject>Palladium</subject><subject>Phosgene</subject><subject>Vanillin</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kE9Lw0AQxRdRsFY_gLeA59WZnW02PUq1WhAU1HPY7B-bkiZ1Ny3m27ulggfxNA_e7z2Gx9glwjUiyZtXBAVSFIBTBICcjtgIcyg40ZSOk0423_un7CzGVUIkShqxxXzbmr7uWt1kdy7UO93XOxezzmeSz7uwHhou-Nr1y-5r2CxdOzTZyxBqW7eOS250qJLR6N6dsxOvm-gufu6Yvc_v32aP_On5YTG7feKGMO95YfxEaY3OWiLQYGCilDVGFhIdKFS20Fo7kIX3zhIQGMorK4wVovKVojG7OvRuQve5dbEvV902pP9jKUgQEqbGROGBMqGLMThfbkK91mEoEcr9YuWfxVJGHDIxse2HC7_N_4e-AXIYbR4</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Potkin, V. 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In particular, the condensation of the title compound with primary amines afforded the corresponding Schiff bases. 4-Formyl-2-methoxyphenyl pyridine-4-carboxylate and one of the Schiff bases derived therefrom were reduced with sodium triacetoxohydridoborate to the corresponding alcohol and amine which were acylated with 5-arylisoxazole- and 4,5-dichloroisothiazole-3-carbonyl chlorides to obtain esters and amides having isoxazole and isothiazole fragments. The synthesized compounds readily formed complexes with palladium(II) chloride, which showed a high catalytic activity in the Suzuki reaction of 3-bromobenzoic acid with 4-methoxyphenylboronic acid in water in the absence of an organic solvent.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070428019100063</doi><tpages>12</tpages></addata></record> |
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subjects | Acylation Amides Amines Carbonyls Catalytic activity Chemical reactions Chemistry Chemistry and Materials Science Chlorides Derivatives Esters Imines Organic Chemistry Palladium Phosgene Vanillin |
title | Functional Derivatives of 4-Formyl-2-methoxyphenyl Pyridine-4-carboxylate |
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