1-(Thiomorpholin-4-ylcarbonyl)-5-[4-(trifluoromethoxy)phenyl]piperidine-3-carboxylic acid → {3-[3-(2-Methoxyethoxy)-1,2,4-oxadiazol-5-yl]-5-[4-(trifluoromethoxy)phenyl]piperidin-1-yl}-(thiomorpholin-4-yl)methanone

Participants

Reaction Steps

According to General Method 1, 300 mg (0.717 mmol) of the compound from Example 9A and 480 mg (2.15 mmol, purity 60%) of 2-methoxyethyl N′-hydroxyimidocarbamate from Example 44A were reacted. Yield: 65 mg (17% of theory).

Provenance & Evidence