Development of C–N coupling processes is fundamentally important and challenging for the synthesis of biologically active molecules and drugs. Herein, we report a highly atom efficient green process for the synthesis of α-ketoamides via visible-light induced copper(I) chloride catalysed direct oxidative Csp–N coupling reactions using commercially available alkynes and anilines at room temperature without
Disclosed are alpha keto amide and alpha hydroxy amide compounds and compositions that inhibit soluble epoxide hydrolase (sEH), methods for preparing the compounds and compositions, and methods for treating patients with such compounds and compositions. The compounds, compositions, and methods are useful for treating a variety of sEH mediated diseases, including hypertensive, cardiovascular, inflammatory, pulmonary, and diabetic-related diseases.
[EN] Disclosed are alpha keto amide and alpha hydroxy amide compounds and compositions that inhibit soluble epoxide hydrolase (sEH), methods for preparing the compounds and compositions, and methods for treating patients with such compounds and compositions. The compounds, compositions, and methods are useful for treating a variety of sEH mediated diseases, including hypertensive, cardiovascular, inflammatory, pulmonary, and diabetic-related diseases. [FR] L'invention concerne des composés alpha-céto amides et alpha-hydroxy amides ainsi que des compositions inhibant l'hydrolase époxyde soluble (sEH), des procédés de préparation de ces composés et compositions, ainsi que des méthodes de traitement de patients mettant en uvre ces composés et compositions. Les composés, compositions et méthodes selon l'invention sont utiles dans le traitement de diverses maladies induites par sEH, notamment les maladies hypertensives, cardiovasculaires, inflammatoires, pulmonaires et les maladies liées au diabète.