反应详情

1-methylethyl[(cis)-1-acetyl-2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydro-4-quinolinyl]carbamate (for a preparation see Intermediate 12) (50 mg, 0.120 mmol) was mixed with 4-bromo-1,3-thiazole-2-carbaldehyde (34.6 mg, 0.180 mmol, available from Frontier), potassium carbonate (33.2 mg, 0.240 mmol), tetrakis(triphenylphosphine)palladium(0) (6.94 mg, 6.01 μmol) and dissolved in ethanol (0.5 mL) and toluene (0.5 mL). The mixture was heated in a nitrogen-flushed microwave vial at 90° C. for 1 hour in a Biotage initiator and the mixture was left to cool to room temperature overnight. The residue was partitioned between distilled water (20 mL) and EtOAc (60 mL). The aqueous layer was extracted with EtOAc (60 mL) and the organic fractions were combined, washed (brine (50 mL)), dried (sodium sulfate), filtered and evaporated to dryness to give a yellow solid. This was purified on a 12+M Biotage silica column eluting with a 0-60% gradient of ethyl acetate in cyclohexane. Product-containing fractions were evaporated to dryness to give a clear, colourless solid (23 mg). LCMS (Method C): Rt=0.96, MH+=402

1. temperatureThe mixture was heated in a nitrogen-
2. customflushed microwave vial at 90° C. for 1 hour in a Biotage initiator
3. waitthe mixture was left
4. customThe residue was partitioned
5. distillationbetween distilled water (20 mL) and EtOAc (60 mL)
6. extractionThe aqueous layer was extracted with EtOAc (60 mL)
7. washwashed (brine (50 mL))
8. dry with materialdried (sodium sulfate)
9. filtrationfiltered
10. customevaporated to dryness
11. customto give a yellow solid
12. customThis was purified on a 12+M Biotage silica column
13. washeluting with a 0-60% gradient of ethyl acetate in cyclohexane
14. customProduct-containing fractions were evaporated to dryness