반응 #799649

ord-ec5cc4237a224950ac30ec8d30f9a10c

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was refluxed for 6 h under N2
  2. 2
    기타quenched with ice-water
  3. 3
    여과filtered
  4. 4
    농축The filtrate was concentrated in vacuo

실험 절차

To a solution of LiAlH4 (1.00 g) in THF was added slowly 2-benzylhexahydro-1H-pyrrolo[3,4-c]pyridine-1,3(2H)-dione (2.00 g) at 0° C. The reaction mixture was refluxed for 6 h under N2, and cooled to rt, quenched with ice-water and filtered. The filtrate was concentrated in vacuo to give the title compound as yellow oil (0.45 g, 25%). The crude product was used for the next step without further purification. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 217.2 (M+1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09181277B2uspto-grants-2015_11