Triethylamine → 4-(3-Hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoic Acid Octadecylamide

Lithocholic acid (81) (9.78 g, 26 mmol) was dissolved in anhydrous tetrahydrofuran (60 mL). Isobutylchloroformate (3.55 g, 3.55 mL, 26 mmol) was added followed by the addition of triethylamine (5.26 g, 7.25 mL, 52 mmol) and dioctadecylamine (7 g, 26 g). The reaction mixture was brought to ambient temperature and allowed to stir over night. The reaction mixture was concentrated under vacuum, and the residue was dissolved in dichloromethane (250 mL). The organic layer was washed with 5% sodium bicarbonate, 3% aqueous HCl and water. After drying over anhydrous sodium sulfate, the solvent was removed under reduced pressure to afford amide 88 (14.5 g) in 89% yield. This was used as such for the next step.

1. customwas brought to ambient temperature
2. concentrationThe reaction mixture was concentrated under vacuum
3. dissolutionthe residue was dissolved in dichloromethane (250 mL)
4. washThe organic layer was washed with 5% sodium bicarbonate, 3% aqueous HCl and water
5. dry with materialAfter drying over anhydrous sodium sulfate
6. customthe solvent was removed under reduced pressure

ORD-Eintrag

ord-739d83eb245047cfa04ceb97f4ffb108

Quelldatensatz

uspto-grants-2016_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09394540B2