Potassium Phosphate, Tribasic → HCID 90203845, compound

HRID 1480281Notes

Reaction equation

HRID 1480281 reaction equation
Br[C:2]1[C:3]([Cl:9])=[CH:4][C:5]([Cl:8])=[N:6][CH:7]=1.[O-]P([O-])([O-])=O.[K+].[K+].[K+].[CH:18]1(B(O)O)[CH2:20][CH2:19]1.C1(P(C2CCCCC2)C2CCCCC2)CCCCC1>C1(C)C=CC=CC=1.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Cl:8][C:5]1[CH:4]=[C:3]([Cl:9])[C:2]([CH:18]2[CH2:20][CH2:19]2)=[CH:7][N:6]=1

Participants

8

Conditions

Temperature
100 °C

Procedure

A mixture of 5-bromo-2,4-dichloro-pyridine (CAN 849937-4, 4 g, 17.63 mmol), potassium phosphate tribasic (11.21 g, 52.89 mmol), cyclopropylboronic acid (5.2 g, 35.84 mmol) in toluene (45 ml) and water (5 ml) was degassed with argon for 15 minutes. To this reaction mixture was added palladium (II) acetate (80 mg, 0.35 mmol) and tricyclohexylphosphine (0.487 g, 1.74 mmol) at 25° C. and reaction mixture was again purged with argon for 5 minutes. The reaction mixture was then stirred at 100° C. for 12 hours. The reaction mixture was cooled to 25° C. and the catalyst was filtered off through a pad of celite and the filter pad was washed with ethyl acetate (3×50 ml). The filtrate was washed with brine, dried over sodium sulfate and evaporated to dryness. The crude material was purified by flash chromatography on silica eluting with a gradient of heptane and ethyl acetate to yield the title compound (2 g, 61%) as a light yellow oil. MS (ESI, m/z): 188.2 (M+H+).

Workup

  1. customwas degassed with argon for 15 minutes
  2. customreaction mixture
  3. customwas again purged with argon for 5 minutes
  4. temperatureThe reaction mixture was cooled to 25° C.
  5. filtrationthe catalyst was filtered off through a pad of celite
  6. washthe filter pad was washed with ethyl acetate (3×50 ml)
  7. washThe filtrate was washed with brine
  8. dry with materialdried over sodium sulfate
  9. customevaporated to dryness
  10. customThe crude material was purified by flash chromatography on silica eluting with a gradient of heptane and ethyl acetate

Sources & evidence

ORD record
ord-12650cf190874bc2bc12636ee73face3
Source dataset
uspto-grants-2016_08
Patent number
US09409866B2

Reaction notes

Loading…