Potassium Carbonate → HCID 24785929, compound

HRID 1023905Notes

Reaction equation

HRID 1023905 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH3:17])=[CH:11][C:10]=2[O:18][CH3:19])=[N:6][CH:7]=1.[CH2:20]([OH:24])[CH2:21][C:22]#[CH:23].C([O-])([O-])=O.[K+].[K+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>COCCOC.[Pd].[Cu]I>[CH3:19][O:18][C:10]1[CH:11]=[C:12]([CH2:15][CH2:16][CH3:17])[CH:13]=[CH:14][C:9]=1[O:8][C:5]1[N:6]=[CH:7][C:2]([C:23]#[C:22][CH2:21][CH2:20][OH:24])=[CH:3][CH:4]=1

Participants

8

Conditions

Temperature
80 °C

Procedure

To a solution of 5-bromo-2-(2-methoxy-4-propylphenoxy)pyridine (0.19 mmol; 60 mg) under argon, in degased DME (1 mL) were added 3-butyn-1-ol (0.47 mmol; 33 mg), Pd/C (0.02 mmol; 42 mg), CuI (0.04 mmol; 7.6 mg), K2CO3 (0.47 mmol; 64 mg), and triphenylphosphine (0.08 mmol; 21 mg). The reaction mixture was stirred at 80° C. overnight, then filtered on celite, washed with ether (3 mL) then ethyl acetate (3 mL). Combined organic phases were washed with saturated NH4Cl (3 mL), dried over MgSO4, concentrated. The residue was purified by preparative TLC (dichloromethane/ethyl acetate) to yield the desired compound as a clear oil (25 mg; 0.08 mmol; 42%).

Workup

  1. filtrationfiltered on celite
  2. washwashed with ether (3 mL)
  3. washCombined organic phases were washed with saturated NH4Cl (3 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customThe residue was purified by preparative TLC (dichloromethane/ethyl acetate)

Sources & evidence

ORD record
ord-356dc60b044642c9b34bb53a24380c45
Source dataset
uspto-grants-2014_05
Patent number
US08722746B2

Reaction notes

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