反应详情

A first stock solution was prepared consisting of 6-(4-iodo-phenoxymethyl)-pyridine-2-carboxylic acid methyl ester (of intermediate 5; 1.77 g, 4.8 mmol), bis(tri -cyclohexyl-phosphine)palladium (available from Strem Chemicals, Inc., Newburyport, Mass.; 168 mg, 0.25 mmol), and dioxane (approximately 100 mL). A second stock solution was prepared consisting of potassium carbonate (1.99 g, 14.4 mmol) and water (approximately 10 mL). The solutions were sonicated and degassed by bubbling nitrogen gas through them. 4 mL of the first stock solution and 0.4 mL of the second stock solution were added to a reaction tube containing 2-methoxymethyl-phenylboronic acid (available from Apollo Scientific Ltd., Stockport, UK; 100 mg, 0.6 mmol). The mixture was heated in a microwave oven at 170 degrees for 25 min, and then 1 M KOH solution (1 equivalent) was added and the reaction mixture was heated in the microwave for 10 minutes at 120 degrees, for 10 minutes at 130 degrees, and at 170 degrees for one hour. The reaction mixture was then filtered through a silica column (1 g) and washed with dimethylacetamide (2×1 mL). The solvent was evaporated to give 6-(2′-methoxymethyl-biphenyl-4-yloxymethyl)-pyridine-2-carboxylic acid. Mass spectrum MH+=350.

1. customA first stock solution was prepared
2. customA second stock solution was prepared
3. customThe solutions were sonicated
4. customdegassed
5. customby bubbling nitrogen gas through them
6. addition4 mL of the first stock solution and 0.4 mL of the second stock solution were added to a reaction tube
7. temperatureThe mixture was heated in a microwave oven at 170 degrees for 25 min
8. temperaturethe reaction mixture was heated in the microwave for 10 minutes at 120 degrees, for 10 minutes at 130 degrees
9. filtrationThe reaction mixture was then filtered through a silica column (1 g)
10. washwashed with dimethylacetamide (2×1 mL)
11. customThe solvent was evaporated