{"title":"二磷酸伯氨喹抗疟疾药物的批量合成。","authors":"Faith M Akwi, Simthandile Swartbooi, Paul Watts","doi":"10.1002/chem.202502183","DOIUrl":null,"url":null,"abstract":"<p><p>An improved three-step synthesis route toward Primaquine Diphosphate is reported herein. The anti-malarial drug was obtained via n-alkylation of readily available potassium phthalimide, followed by reductive amination and room temperature methylaminolysis-assisted phthalimido deprotection of the key intermediates to furnish Primaquine Diphosphate in 47% overall isolated yield.</p>","PeriodicalId":144,"journal":{"name":"Chemistry - A European Journal","volume":" ","pages":"e02183"},"PeriodicalIF":3.7000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Batch Synthesis of Primaquine Diphosphate Anti-Malarial Drug.\",\"authors\":\"Faith M Akwi, Simthandile Swartbooi, Paul Watts\",\"doi\":\"10.1002/chem.202502183\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>An improved three-step synthesis route toward Primaquine Diphosphate is reported herein. The anti-malarial drug was obtained via n-alkylation of readily available potassium phthalimide, followed by reductive amination and room temperature methylaminolysis-assisted phthalimido deprotection of the key intermediates to furnish Primaquine Diphosphate in 47% overall isolated yield.</p>\",\"PeriodicalId\":144,\"journal\":{\"name\":\"Chemistry - A European Journal\",\"volume\":\" \",\"pages\":\"e02183\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - A European Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/chem.202502183\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - A European Journal","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/chem.202502183","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Batch Synthesis of Primaquine Diphosphate Anti-Malarial Drug.
An improved three-step synthesis route toward Primaquine Diphosphate is reported herein. The anti-malarial drug was obtained via n-alkylation of readily available potassium phthalimide, followed by reductive amination and room temperature methylaminolysis-assisted phthalimido deprotection of the key intermediates to furnish Primaquine Diphosphate in 47% overall isolated yield.
期刊介绍:
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