Two Approaches to a Trifluoromethyl Triazole: A Fit-for-Purpose Trifluoromethylation in Flow-Mode and a Long-Term Decarboxylative Click Approach

被引:9
作者
Ayothiraman, Rajaram [1 ]
Gangu, Aravind S. [1 ]
Bandaru, Durgarao [1 ]
Guturi, Siva Krishna [1 ]
Lakshminarasimhan, Thirumalai [1 ]
Jaleel, Mohamed [1 ]
Kanagavel, Kishorekumar [1 ]
Rangaswamy, Sundaramurthy [1 ]
Cuniere, Nicolas L. [1 ]
Zaretsky, Serge [1 ]
Camacho, Kathryn [1 ]
Eastgate, Martin D. [1 ]
Vaidyanathan, Rajappa [1 ]
机构
[1] Biocon Bristol Myers Squibb Res & Dev Ctr, Chem Dev & API Supply, Bengaluru 560099, India
关键词
trifluoromethylation; iodotriazole; decarboxylative Click; CuAAC; MDFA; scale-up in flow; CSTR; ARYL IODIDES; COPPER; REAGENT; CASCADE; ACIDS;
D O I
10.1021/acs.oprd.9b00492
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two approaches to a 1-aryl-4-trifluoromethyltriazole are described. Initially, a late-stage trifluoromethylation of the corresponding 1-aryl-4-iodotriazole using methyl fluorosulfonyldifluoroacetate (MDFA) was employed. However, the reaction was fraught with several safety and operational challenges, primarily due to the evolution of similar to 33 equiv of gas per equiv of substrate. While some of these challenges were either addressed or mitigated through operations in plug flow, the process remained low yielding and suboptimal. Subsequently, a more convergent, longer-term route involving a Cu-mediated decarboxylative Click reaction was developed.
引用
收藏
页码:207 / 215
页数:9
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