{"title":"以水为溶剂微波辅助合成一种新型嘧啶核希夫碱同系物的方案:绿色合成方法","authors":"D. Karati, K. Mahadik, Dileep Kumar","doi":"10.2174/2213335609666220414141731","DOIUrl":null,"url":null,"abstract":"\n\nThe research work aims to develop sustainable microwave-assisted scheme for the synthesis of 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile congeners.\n\n\n\n4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds are novel molecules having various pharmacological activities such as neurodegenerative, anti-microbial, anti-cancer. Schiff base congeners are considered as efficient pharmacophores for research. These activities are due to the presence of azomethine (CH=N) group in the Schiff base compounds.\n\n\n\nTo synthesise different novel Schiff base scaffolds of pyrimidine nuclei by green chemistry with good yield.\n\n\n\nThe 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds were prepared by two step reactions. Both steps were microwave assisted. The first step was to synthesize 4-amino-6-phenylpyrimidine-5-carbonitrile as intermediate compound. This compound was synthesized by using benzaldehyde, malononitrile and formamidine hydrochloride. The reaction conditions are as following: \ntemperature- 1010C, pressure- 300W, time- 50min.\nThe final Schiff base congeners were obtained by reacting it with various aromatic aldehydes in the second step. The yield, reaction condition, and time consumption all were very acceptable for the green synthetic methods rather than the conventional schemes.\n\n\n\nMicrowave assisted method was more efficient. The reactions were less time consuming and the overall yield of the all-synthesized compounds was in the range of 72-81%. The synthesized congeners were characterized by different spectroscopic methods. The main functional group [azomethine] was considered by the IR peak at 1611 cm-1 wavelength.\n\n\n\nThis microwave assisted synthetic method thus emerges as more eco-friendly due to a much-reduced usage of organic solvents, leading to less harmful residues. Using this scheme, we synthesized different Schiff base congeners with satisfactory chemical yields.\n","PeriodicalId":43539,"journal":{"name":"Current Microwave Chemistry","volume":" ","pages":""},"PeriodicalIF":0.9000,"publicationDate":"2022-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Microwave assisted synthetic scheme of a novel Schiff base congeners of pyrimidine nuclei by using water as solvent: green approach of synthesis\",\"authors\":\"D. Karati, K. Mahadik, Dileep Kumar\",\"doi\":\"10.2174/2213335609666220414141731\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nThe research work aims to develop sustainable microwave-assisted scheme for the synthesis of 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile congeners.\\n\\n\\n\\n4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds are novel molecules having various pharmacological activities such as neurodegenerative, anti-microbial, anti-cancer. Schiff base congeners are considered as efficient pharmacophores for research. These activities are due to the presence of azomethine (CH=N) group in the Schiff base compounds.\\n\\n\\n\\nTo synthesise different novel Schiff base scaffolds of pyrimidine nuclei by green chemistry with good yield.\\n\\n\\n\\nThe 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds were prepared by two step reactions. Both steps were microwave assisted. The first step was to synthesize 4-amino-6-phenylpyrimidine-5-carbonitrile as intermediate compound. This compound was synthesized by using benzaldehyde, malononitrile and formamidine hydrochloride. The reaction conditions are as following: \\ntemperature- 1010C, pressure- 300W, time- 50min.\\nThe final Schiff base congeners were obtained by reacting it with various aromatic aldehydes in the second step. The yield, reaction condition, and time consumption all were very acceptable for the green synthetic methods rather than the conventional schemes.\\n\\n\\n\\nMicrowave assisted method was more efficient. The reactions were less time consuming and the overall yield of the all-synthesized compounds was in the range of 72-81%. The synthesized congeners were characterized by different spectroscopic methods. The main functional group [azomethine] was considered by the IR peak at 1611 cm-1 wavelength.\\n\\n\\n\\nThis microwave assisted synthetic method thus emerges as more eco-friendly due to a much-reduced usage of organic solvents, leading to less harmful residues. Using this scheme, we synthesized different Schiff base congeners with satisfactory chemical yields.\\n\",\"PeriodicalId\":43539,\"journal\":{\"name\":\"Current Microwave Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2022-04-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Microwave Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2213335609666220414141731\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Microwave Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2213335609666220414141731","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Microwave assisted synthetic scheme of a novel Schiff base congeners of pyrimidine nuclei by using water as solvent: green approach of synthesis
The research work aims to develop sustainable microwave-assisted scheme for the synthesis of 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile congeners.
4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds are novel molecules having various pharmacological activities such as neurodegenerative, anti-microbial, anti-cancer. Schiff base congeners are considered as efficient pharmacophores for research. These activities are due to the presence of azomethine (CH=N) group in the Schiff base compounds.
To synthesise different novel Schiff base scaffolds of pyrimidine nuclei by green chemistry with good yield.
The 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds were prepared by two step reactions. Both steps were microwave assisted. The first step was to synthesize 4-amino-6-phenylpyrimidine-5-carbonitrile as intermediate compound. This compound was synthesized by using benzaldehyde, malononitrile and formamidine hydrochloride. The reaction conditions are as following:
temperature- 1010C, pressure- 300W, time- 50min.
The final Schiff base congeners were obtained by reacting it with various aromatic aldehydes in the second step. The yield, reaction condition, and time consumption all were very acceptable for the green synthetic methods rather than the conventional schemes.
Microwave assisted method was more efficient. The reactions were less time consuming and the overall yield of the all-synthesized compounds was in the range of 72-81%. The synthesized congeners were characterized by different spectroscopic methods. The main functional group [azomethine] was considered by the IR peak at 1611 cm-1 wavelength.
This microwave assisted synthetic method thus emerges as more eco-friendly due to a much-reduced usage of organic solvents, leading to less harmful residues. Using this scheme, we synthesized different Schiff base congeners with satisfactory chemical yields.