反应详情

温度

50 °C

A solution of 2-(4-bromo-2-fluorophenyl)-2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)ethyl acetate (0.345 mmol) in 1,4-dioxane (1.5 mL) was treated with 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline (0.380 mmol), PdCl2(dppf)-CH2Cl2 adduct (0.017 mmol), and 2M aq potassium carbonate (1.035 mmol). The reaction vessel was purged with nitrogen and sealed, and the mixture irradiated in a Biotage Initiator Microwave at 120° C. for 15 min. The mixture was then concentrated to dryness in vacuo. The brown residue was diluted with ethanol (2 mL) and the solution was stirred in an oil bath at 50° C. overnight, after which the reaction was concentrated to dryness under a stream of nitrogen. The crude material was suspended in water (50 mL) and was extracted three times with ethyl acetate. The aqueous layer was further diluted with brine (20 mL) and was extracted once more with tetrahydrofuran. The organic layers (ethyl acetate and tetrahydrofuran) were combined, dried over sodium sulfate, filtered and concentrated in vacuo. Purification of the residue by silica gel chromatography (0-6% methanol/dichloromethane) and chiral HPLC (Chromegachiral CC4, methanol) afforded the title compound as a white solid in >98% ee (21 mg, 12% yield). MS(ES)+ m/e 476.1 [M+H]+. αD=+ 20 deg (c=0.04, methanol).

1. customThe reaction vessel was purged with nitrogen
2. customsealed
3. customthe mixture irradiated in a Biotage Initiator Microwave at 120° C. for 15 min
4. concentrationThe mixture was then concentrated to dryness in vacuo
5. additionThe brown residue was diluted with ethanol (2 mL)
6. concentrationafter which the reaction was concentrated to dryness under a stream of nitrogen
7. extractionwas extracted three times with ethyl acetate
8. additionThe aqueous layer was further diluted with brine (20 mL)
9. extractionwas extracted once more with tetrahydrofuran
10. dry with materialdried over sodium sulfate
11. filtrationfiltered
12. concentrationconcentrated in vacuo
13. customPurification of the residue by silica gel chromatography (0-6% methanol/dichloromethane) and chiral HPLC (Chromegachiral CC4, methanol)