{"title":"JAK抑制剂培非替尼的合成及合成工艺优化研究","authors":"珊 刘","doi":"10.12677/hjmce.2022.102016","DOIUrl":null,"url":null,"abstract":"Peficitinib is a novel Janus kinase 1 and Janus kinase 3 inhibitor developed by Astellas, a Japa-nese company. Peficitinib mainly treats the moderate or severe rheumatoid arthritis with in-刘珊 adequate response to methotrexate. At present, there are very few papers on the synthesis route of Peficitinib. In this paper, a complete synthesis route is designed, and then each step of the reaction is studied and optimized. Starting from 7-azindole, the target compound was obtained through seven steps including halogenation, substitution (upper protection), esterification, de-protection, ester hydrolysis, amidation and then substitution. By providing catalyst or changing other reaction conditions such as solvent, temperature and molar ratio of reactants, a reasona-ble route, high yield, short time and simple operation of Peficitinib synthesis process was suc-cessfully obtained, and the synthesis of Peficitinib can reach industrial production. The struc-tures of the target compounds and intermediates were confirmed by 1 H NMR, and the total yield of the route was 32.8%.","PeriodicalId":64647,"journal":{"name":"药物化学","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Study on Synthesis and Optimization of Syn-thesis Technology of JAK Inhibitor Peficitinib\",\"authors\":\"珊 刘\",\"doi\":\"10.12677/hjmce.2022.102016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Peficitinib is a novel Janus kinase 1 and Janus kinase 3 inhibitor developed by Astellas, a Japa-nese company. Peficitinib mainly treats the moderate or severe rheumatoid arthritis with in-刘珊 adequate response to methotrexate. At present, there are very few papers on the synthesis route of Peficitinib. In this paper, a complete synthesis route is designed, and then each step of the reaction is studied and optimized. Starting from 7-azindole, the target compound was obtained through seven steps including halogenation, substitution (upper protection), esterification, de-protection, ester hydrolysis, amidation and then substitution. By providing catalyst or changing other reaction conditions such as solvent, temperature and molar ratio of reactants, a reasona-ble route, high yield, short time and simple operation of Peficitinib synthesis process was suc-cessfully obtained, and the synthesis of Peficitinib can reach industrial production. The struc-tures of the target compounds and intermediates were confirmed by 1 H NMR, and the total yield of the route was 32.8%.\",\"PeriodicalId\":64647,\"journal\":{\"name\":\"药物化学\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"药物化学\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.12677/hjmce.2022.102016\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"药物化学","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.12677/hjmce.2022.102016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Study on Synthesis and Optimization of Syn-thesis Technology of JAK Inhibitor Peficitinib
Peficitinib is a novel Janus kinase 1 and Janus kinase 3 inhibitor developed by Astellas, a Japa-nese company. Peficitinib mainly treats the moderate or severe rheumatoid arthritis with in-刘珊 adequate response to methotrexate. At present, there are very few papers on the synthesis route of Peficitinib. In this paper, a complete synthesis route is designed, and then each step of the reaction is studied and optimized. Starting from 7-azindole, the target compound was obtained through seven steps including halogenation, substitution (upper protection), esterification, de-protection, ester hydrolysis, amidation and then substitution. By providing catalyst or changing other reaction conditions such as solvent, temperature and molar ratio of reactants, a reasona-ble route, high yield, short time and simple operation of Peficitinib synthesis process was suc-cessfully obtained, and the synthesis of Peficitinib can reach industrial production. The struc-tures of the target compounds and intermediates were confirmed by 1 H NMR, and the total yield of the route was 32.8%.