Reaction #680083

ord-3e3d65bb964d481591908c904371fa0b

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherA 50-mL round-bottomed flask equipped with a reflux condenser
  2. 2
    OtherAfter three cycles of vacuum/argon flush
  3. 3
    FiltrationIt was then filtered
  4. 4
    Otherthe filtrate was evaporated in vacuo
  5. 5
    OtherThe residue was purified by silica-gel column chromatography
  6. 6
    Washeluting with 1:20 methanol/dichloromethane

Procedure

A 50-mL round-bottomed flask equipped with a reflux condenser was charged with 218a (130 mg, 0.44 mmol), (3-(acetoxymethyl)-2-(7,7-dimethyl-1-oxo-3,4,7,8-tetrahydro-1H-cyclo-penta[4,5]pyrrolo[1,2-a]pyrazin-2(6H)-yl)pyridin-4-yl)boronic acid 199e (175 mg, 0.44 mmol), PdCl2(dppf) (36 mg, 0.044 mmol), K3PO4 (343 mg, 1.32 mmol), sodium acetate (108 mg, 1.32 mmol), acetonitrile (10 mL), and water (0.5 mL). After three cycles of vacuum/argon flush, the mixture was heated at 100° C. for 3 h. It was then filtered and the filtrate was evaporated in vacuo. The residue was purified by silica-gel column chromatography eluting with 1:20 methanol/dichloromethane to afford 218b as a red solid (103 mg, 42%). MS-ESI: [M+H]+ 570.2

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09238655B2uspto-grants-2016_01