Triethylamine → (S)-1-(3-chloro-5-fluoropyridin-4-yl)-4-(tetrahydrofuran-3-yl)piperazine

MsCl (393.3 mg, 265.7 μL, 3.433 mmol) was added to a solution of (3R)-tetrahydrofuran-3-ol (275 mg, 3.121 mmol) and Et3N (379.0 mg, 522.0 μL, 3.745 mmol) in DCM (5 mL) at 0° C. and the resulting solution stirred at RT overnight. The reaction mixture was diluted with water (5 mL) and DCM (5 mL) and the layers separated. The aqueous layer was extracted further with DCM (2×5 mL) and the combined organic extracts washed with saturated aqueous sodium hydrogen carbonate solution (1×5 mL), dried over MgSO4 and concentrated in vacuo. The residue was taken up in n-BuOH (5 mL) and 1-(3-chloro-5-fluoro-4-pyridyl)piperazine (1.010 g, 4.682 mmol) was added and the reaction mixture heated at 118° C. overnight. The reaction mixture was cooled to RT and concentrated in vacuo. The residue was purified by column chromatography on silica (24 g column, 0-100% EtOAc/petroleum ether). Product fractions were combined and concentrated in vacuo to leave (S)-1-(3-chloro-5-fluoropyridin-4-yl)-4-(tetrahydrofuran-3-yl)piperazine as an off white solid. MS (ES+) 288.1.

1. customthe layers separated
2. extractionThe aqueous layer was extracted further with DCM (2×5 mL)
3. washthe combined organic extracts washed with saturated aqueous sodium hydrogen carbonate solution (1×5 mL)
4. dry with materialdried over MgSO4
5. concentrationconcentrated in vacuo
6. temperaturethe reaction mixture heated at 118° C. overnight
7. temperatureThe reaction mixture was cooled to RT
8. concentrationconcentrated in vacuo
9. customThe residue was purified by column chromatography on silica (24 g column, 0-100% EtOAc/petroleum ether)
10. concentrationconcentrated in vacuo

ORD record

ord-01125090ff754576a44bccd5281d698d

Source dataset

uspto-grants-2016_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09340546B2