(4-bromo-2-methylphenyl)-morpholin-4-ylmethanone

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Prepared analogously to Example 1g from N-(4-bromo-2-methyl-benzoyl)-morpholine, propargyl alcohol, tetrakis(triphenylphosphine)palladium(0), copper(I)iodide and triethylamine in acetonitrile.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Prepared analogously to Example 1g from N-(4-bromo-2-methyl-benzoyl)-morpholine, propargyl alcohol, tetrakis(triphenylphosphine)palladium(0), copper(I)iodide and triethylamine in acetonitrile.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A solution of 10.6 ml (47 mmol) oxalyl chloride in 30 ml dichloromethane is added dropwise to a iced-cooled solution of 5.21 g (23.5 mmol) 4-bromo-2-methyl-benzoic acid and 0.0087 ml DMF in 100 ml CH2Cl2. After complete addition, the cooling bath is removed and stirring maintained for 2 h at RT. The solvent is evaporated to dryness and the residue is dried in vacuo and dissolved in 100 ml dichloromethane and 8.21 ml N-ethyl-diisopropylamine is added. To this solution 2.5 ml (28 mmol) morpholine is added slowly. Stirring is continued for 0.5 h, then the reaction mixture is poured on water and extracted 3× with EtOAc. The combined organic layers are washed with water and saturated NaCl solution, dried over MgSO4, filtered and the filtrate is concentrated in vacuo to afford the title compound which is used in the next step without further purification. After complete addition the cooling bath is removed The solvent is evaporated to dryness the residue is dried in vacuo dissolved in 100 ml dichloromethane 8.21 ml N-ethyl-diisopropylamine is added Stirring the reaction mixture is poured on water extracted 3× with EtOAc The combined organic layers are washed with water and saturated NaCl solution dried over MgSO4 filtered the filtrate is concentrated in vacuo

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Prepared analogously to Example 1g from N-(4-bromo-2-methyl-benzoyl)-morpholine, propargyl alcohol, tetrakis(triphenylphosphine)palladium(0), copper(I)iodide and triethylamine in acetonitrile.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A solution of 10.6 ml (47 mmol) oxalyl chloride in 30 ml dichloromethane is added dropwise to a iced-cooled solution of 5.21 g (23.5 mmol) 4-bromo-2-methyl-benzoic acid and 0.0087 ml DMF in 100 ml CH2Cl2. After complete addition, the cooling bath is removed and stirring maintained for 2 h at RT. The solvent is evaporated to dryness and the residue is dried in vacuo and dissolved in 100 ml dichloromethane and 8.21 ml N-ethyl-diisopropylamine is added. To this solution 2.5 ml (28 mmol) morpholine is added slowly. Stirring is continued for 0.5 h, then the reaction mixture is poured on water and extracted 3× with EtOAc. The combined organic layers are washed with water and saturated NaCl solution, dried over MgSO4, filtered and the filtrate is concentrated in vacuo to afford the title compound which is used in the next step without further purification. After complete addition the cooling bath is removed The solvent is evaporated to dryness the residue is dried in vacuo dissolved in 100 ml dichloromethane 8.21 ml N-ethyl-diisopropylamine is added Stirring the reaction mixture is poured on water extracted 3× with EtOAc The combined organic layers are washed with water and saturated NaCl solution dried over MgSO4 filtered the filtrate is concentrated in vacuo