Réaction #90512

ord-91e0d8a9e1ae4f0c8f4fbc35dca47205

Solvants

Conditions de réaction

Température
110°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction was degassed
  2. 2
    Autrepurged with nitrogen for 10 min
  3. 3
    Autredegassed
  4. 4
    Autrepurged and with nitrogen for another 10 min
  5. 5
    Autreunder sealed microwave vial
  6. 6
    workup.ADDITIONAfter completion of the starting material, the reaction was diluted with chloroform
  7. 7
    Filtrationfiltered through celite bed
  8. 8
    ConcentrationThe organic layer was concentrated

Mode opératoire

A solution of 5-bromo-6-methoxy-2,3-dihydro-1H-inden-1-one (11) (1 g, 4.149 mmol) and morpholine (0.36 g, 4.149 mmol) in toluene 15 mL was added cesium carbonate (2.69 g, 8.298 mmol). The reaction was degassed and purged with nitrogen for 10 min. Pd2(dba)3 (189.3 mg, 0.207 mmol) and BINAP (64.5 mg, 0.103 mmol) was added, degassed and purged and with nitrogen for another 10 min. The reaction was heated to 110° C. overnight under sealed microwave vial. After completion of the starting material, the reaction was diluted with chloroform and filtered through celite bed. The organic layer was concentrated to get the crude compound 13 and the resulting crude was purified through flash chromatography by using 100-200 mesh silica gel eluting the compound at 25% ethyl acetate in hexane as pale yellow coloured solid 6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 13. 1HNMR (400 MHz, CDCl3) δ ppm 7.70 (s, 1H), 7.20 (s, 1H), 3.93 (s, 3H), 3.06 (m, 2H), 2.72 (m, 2H); MS (ESI) m/z 247.9 (M+H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09446047B2uspto-grants-2016_09