Cesium carbonate → HCID 66721782, compound

HRID 1526156Notes

Reaction equation

HRID 1526156 reaction equation
[CH:1]1([B-](F)(F)F)[CH2:3][CH2:2]1.[K+].C12(C(C34CC5CC(CC(C5)C3)C4)CCCP)CC3CC(CC(C3)C1)C2.C([O-])([O-])=O.[Cs+].[Cs+].Cl[C:41]1[CH:46]=[C:45]([N+:47]([O-:49])=[O:48])[CH:44]=[CH:43][N:42]=1>C1(C)C=CC=CC=1.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:1]1([C:41]2[CH:46]=[C:45]([N+:47]([O-:49])=[O:48])[CH:44]=[CH:43][N:42]=2)[CH2:3][CH2:2]1

Participants

8

Conditions

Temperature
98 °C

Procedure

To a mixture of potassium cyclopropyltrifluoroborate (0.943 g, 6.37 mmol), palladium (II) acetate (0.0285 g, 0.126 mmol), di-1-adamantylbutylphosphine [CAS 321921-71-5] (0.0678 g, 0.189 mmol) and Cs2CO3 (6.165 g, 18.922 mmol) in toluene (20 ml) and water (4 ml) under a nitrogen atmosphere was added 2-chloro-4-nitropyridine (1 g, 6.307 mmo). The reaction mixture was heated at 98° C. for 2 days. After cooling, the mixture was washed with water. The organic phase was separated and dried (Na2SO4). The filtrate was concentrated in vacuo and the residue was purified by column chromatography (silica gel; Heptane/DCM from 100/0 to 50/50 as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate compound D52 (0.800 g, 77%) as yellow oil which crystallized upon standing

Workup

  1. temperatureAfter cooling
  2. washthe mixture was washed with water
  3. customThe organic phase was separated
  4. dry with materialdried (Na2SO4)
  5. concentrationThe filtrate was concentrated in vacuo
  6. customthe residue was purified by column chromatography (silica gel; Heptane/DCM from 100/0 to 50/50 as eluent)
  7. customThe desired fractions were collected
  8. concentrationconcentrated in vacuo
  9. customto yield intermediate compound D52 (0.800 g, 77%) as yellow oil which
  10. customcrystallized

Sources & evidence

ORD record
ord-5b305712a51643708b26a638872f78e5
Source dataset
uspto-grants-2015_07
Patent number
US09085577B2

Reaction notes

Loading…