Sodium hydride → N-[4-fluoro-3-(trifluoromethyl)phenyl]-2,4-dioxobicyclo[3.2.1]octane-3-carboxamide

Sodium hydride (60% dispersion in mineral oil, 0.064 g, 1.59 mmol) was washed with dry hexane under a nitrogen atmosphere to remove mineral oil. It was then suspended in dry tetrahydrofuran (3 mL). To the suspension was added a solution of 2,4-dioxobicyclo[3.2.1]octane (0.20 g, 1.45 mmol) in dry tetrahydrofuran (10 mL). The resulting mixture was stirred at room temperature under a nitrogen atmosphere overnight. It was then treated with 4-fluoro-3-(trifluoromethyl)phenyl isocynate (0.31 mL, 2.17 mmol) via syringe. The resulting mixture was stirred at room temperature under a nitrogen atmosphere overnight. The reaction mixture was then concentrated on a rotary evaporator and the residue was partitioned between dichloromethane (150 mL) and 1N aqueous HCl (100 mL). The aqueous layer was extracted twice with additional portions of dichloromethane ((25 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated on a rotary evaporator. The desired product was isolated by chromatrography on silica gel (2% methanol/dichloromethane) to yield the title compound as a light yellow solid (0.36 g, 73% yield), mp=97–100° C.; MS (−) ESI m/z=342 (M−H)−.

1. customto remove mineral oil
2. stirringThe resulting mixture was stirred at room temperature under a nitrogen atmosphere overnight
3. concentrationThe reaction mixture was then concentrated on a rotary evaporator
4. customthe residue was partitioned between dichloromethane (150 mL) and 1N aqueous HCl (100 mL)
5. extractionThe aqueous layer was extracted twice with additional portions of dichloromethane ((25 mL)
6. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
7. concentrationconcentrated on a rotary evaporator

ORD record

ord-a7b0de248b9d4a50b8bf6c95c1f44ba0

Source dataset

uspto-grants-2007_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07179943B2