Methanol → HCID 67428674, compound

To a stirred solution of N-(1-benzylpiperidin-4-yl)-N-isopropyl 3-(bromopropoxy)propionamide (28.2 g, 66 mmol) in THF (300 mL) was added BH3-THF (100 mL, 2.0 M in THF, 200 mmol) and the reaction mixture was refluxed for 48 h. The reaction mixture was then allowed to cool to room temperature and methanol was added dropwise until evolution of hydrogen gas stopped. The mixture was then concentrated under reduced pressure and dissolved in dichloromethane (500 mL). The reaction mixture was washed with 1 N hydrochloric acid (500 mL) and the organic layer removed. The aqueous layer was then made basic to pH 12 using 1 N sodium hydroxide and extracted with dichloromethane (500 mL). The combined organic layers were washed with water (400 mL), brine (400 mL), dried over anhydrous magnesium sulfate and the solvent removed under reduced pressure. The resulting crude product was purified by silica gel chromatography (dichloromethane/methanol/aqueous ammonia: 9/0.5/0.05) to afford 20.5 g of the title intermediate (76% yield).

1. temperaturethe reaction mixture was refluxed for 48 h
2. concentrationThe mixture was then concentrated under reduced pressure
3. dissolutiondissolved in dichloromethane (500 mL)
4. washThe reaction mixture was washed with 1 N hydrochloric acid (500 mL)
5. customthe organic layer removed
6. extractionextracted with dichloromethane (500 mL)
7. washThe combined organic layers were washed with water (400 mL), brine (400 mL)
8. dry with materialdried over anhydrous magnesium sulfate
9. customthe solvent removed under reduced pressure
10. customThe resulting crude product was purified by silica gel chromatography (dichloromethane/methanol/aqueous ammonia: 9/0.5/0.05)

ORD record

ord-6defe51d7c2c40ae8ef00f73795b447a

Source dataset

uspto-grants-2011_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08080565B2