Potassium Carbonate → HCID 24785929, compound
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]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
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
- filtrationfiltered on celite
- washwashed with ether (3 mL)
- washCombined organic phases were washed with saturated NH4Cl (3 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated
- 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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