반응 #1280520

ord-7c42841d50d44e3d9072a2a62eb7f34e

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타degassed for 30 min with nitrogen
  2. 2
    workup.ADDITION20% Pd—(OH)2 (200 mg) was added
  3. 3
    여과the reaction mixture was filtered off over Celite
  4. 4
    세척washed with MeOH (3×25 ml)
  5. 5
    농축the filtrate was concentrated under reduced pressure

실험 절차

N-Benzyl-N-methyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamine (1.4 g, 3.63 mmol, 1 eq) was dissolved in MeOH (20 ml) and degassed for 30 min with nitrogen. 20% Pd—(OH)2 (200 mg) was added and hydrogenation was carried out for 2 h at RT under balloon pressure (H2). After monitoring by thin-layer chromatography, the reaction mixture was filtered off over Celite and washed with MeOH (3×25 ml), and the filtrate was concentrated under reduced pressure. Yield: 30% (240 mg, 1.09 mmol).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08680159B2uspto-grants-2014_03