反应详情

温度

100 °C

A mixture of 1-chloro-2-ethynylbenzene (0.63 g, 4.6 mmol), 5-bromo-2-methylsulfanylpyrimidine-4-carboxylic acid methyl ester (1.0 g, 3.8 mmol), triethylamine (2.5 ml), triphenylphosphine (0.125 g, 0.48 mmol), copper (I) iodide (0.025 g, 0.13 mmol), bistriphenyphosphinepalladium (II) dichloride (0.10 g, 0.14 mmol) and dimethylformamide (1 ml) was stirred in a heavy-walled Smith process vial and irradiated with microwaves to maintain 100° C. for 20 min. The mixture was diluted with dichloromethane (20 ml) and washed with 5% hydrochloric acid (20 ml), water (20 ml), saturated aqueous sodium hydrogencarbonate solution (20 ml) and water (20 ml) then dried (MgSO4) and evaporated in vacuo. The residual oil was purified by flash column chromatography over silica using a 1:4 mixture of hexane and dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 5-(2-chlorophenylethynyl)-2-methylsulfanylpyrimidine-4-carboxylic acid methyl ester (0.9 g) as a yellow oil. 250 MHz 1H-NMR (CDCl3) δ (ppm): 2.5 (s, 3H) (—SCH3), 3.9 (s, 3H) (—CO2CH3), 7.1-7.5 (m, 4H) (ArH), 8.65 (s, 1H) (ArH); m/z (M+H)+. 319, HPLC purity 91%, HPLC retention time 4.08 min.

1. customirradiated with microwaves
2. washwashed with 5% hydrochloric acid (20 ml), water (20 ml), saturated aqueous sodium hydrogencarbonate solution (20 ml) and water (20 ml)
3. dry with materialthen dried (MgSO4)
4. customevaporated in vacuo
5. customThe residual oil was purified by flash column chromatography over silica using
6. additiona 1:4 mixture of hexane and dichloromethane as eluant
7. customthe solvents removed in vacuo