反应详情

A solution of 4-(4-bromophenyl)-5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-one (0.256 mmol) in 1,4-dioxane (1.5 mL) was treated with 2-methyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3-thiazole (0.281 mmol), dichloro[1,1′-bis(diphenylphosphino) ferrocene]palladium (II)-dichloromethane adduct (10 mg) and 2M aq potassium carbonate (0.767 mmol). The reaction mixture was purged with nitrogen, sealed, and irradiated in a microwave at 150° C. for 15 min. The reaction mixture was cooled to room temperature and was diluted with water (50 mL). The aqueous layer was acidified to pH˜4 using 1N aq HCl and was extracted with dichloromethane. The organic layer was dried over sodium sulfate, treated with Si-Thiol (Silicycle, 20 mg), filtered, and concentrated in vacuo. The crude residue was purified by reverse phase HPLC (25-55% acetonitrile w/0.1% TFA/water w/0.1% TFA). The product fractions from the HPLC were combined, adjusted to pH˜5 with the addition of saturated aq sodium bicarbonate, and extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting product was then purified by flash chromatography (3-10% methanol/dichloromethane) to afford the title compound as an amorphous white solid (40%). MS(ES)+ m/e 486.2 [M+H]+.

1. customThe reaction mixture was purged with nitrogen
2. customsealed
3. customirradiated in a microwave at 150° C. for 15 min
4. additionwas diluted with water (50 mL)
5. extractionwas extracted with dichloromethane
6. dry with materialThe organic layer was dried over sodium sulfate
7. additiontreated with Si-Thiol (Silicycle, 20 mg)
8. filtrationfiltered
9. concentrationconcentrated in vacuo
10. customThe crude residue was purified by reverse phase HPLC (25-55% acetonitrile w/0.1% TFA/water w/0.1% TFA)
11. additionadjusted to pH˜5 with the addition of saturated aq sodium bicarbonate
12. extractionextracted with dichloromethane
13. dry with materialThe organic layer was dried over magnesium sulfate
14. filtrationfiltered
15. concentrationconcentrated in vacuo
16. customThe resulting product was then purified by flash chromatography (3-10% methanol/dichloromethane)