반응 #835839

ord-78ea6384b3db404a9266c767ef978e2d

반응 방정식

CCOCC
ether
N#Cc1nccc2ccccc12
isoquinoline-1-carbonitrile
[CH3][Mg][Br]
methylmagnesium bromide
CC(=O)c1nccc2ccccc12
1-isoquinolin-1-yl-ethanone
수율 75.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The mixture was quenched with a sat. solution of NH4Cl
  2. 2
    추출extracted with ethyl acetate
  3. 3
    건조The organic layers were dried over MgSO4
  4. 4
    여과filtered
  5. 5
    농축concentrated under reduced pressure
  6. 6
    기타The material was purified by chromatography on silica gel with 10% ethyl acetate

실험 절차

A solution of isoquinoline-1-carbonitrile (Intemediate H1) (commercially available from Aldrich) (4.40 g, 28.5 mmol) in THF at 0° C. was treated with methylmagnesium bromide (20 mL, of a 3M soln in ether) for 3 h. (see procedure found in Vacher, B. et al J. Med. Chem. 1998 41, 5070; incorporated herein by reference). The mixture was quenched with a sat. solution of NH4Cl and stirred for 3 h at rt. The aqueous layer was basified with NaOH and extracted with ethyl acetate. The organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The material was purified by chromatography on silica gel with 10% ethyl acetate: hexane to give 1-isoquinolin-1-yl-ethanone (Intermediate H2) 3.65 g (75%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07399868B2uspto-grants-2008_07