4-(5-(3,6-Dihydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline → 4-(5-(Tetrahydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline

Participants

Reaction Conditions

Reaction Steps

To a pressure vessel was added palladium hydroxide, palladium on carbon (396 mg, 2.82 mmol), ethanol (18.800 ml), and 4-(5-(3,6-dihydro-2H-pyran-4-yl)pyrimidin-4-yloxy)aniline (760 mg, 2.82 mmol). The vessel was purged of air and backfilled with hydrogen (45 psi) before heating to 50° C. for 60 h. It was cooled to room temperature, filtered through Celite, and concentrated under reduced pressure to afford the product as a dark yellow oil. MS (ESI, pos. ion) m/z: 272.1 (M+1).

Provenance & Evidence