反应详情

Into a 50 mL single neck flask, 1 mL oxalyl chloride was added syringe wise to 4-[4-(1-fluoro-1-methyl-2-{[(methylethyl)sulfonyl]amino}ethyl)phenyl]benzoic acid (150 mg, 0.40 mmol, prepared in example 4) in CH2Cl2 (10 mL) while stirring under nitrogen at room temperature. Immediately, 1 drop of DMF was added by pipette initiating a foaming of the mixture. The reaction was stirred one hour at this temperature and then concentrated under reduced vacuum to yield a white semi-solid. This material was placed into THF (10 mL) and added dropwise to a stirring solution of 40% methylamine in water (5 mL) at room temperature and the mixture was stirred overnight. In the morning, the solution was concentrated under reduced vacuum and the resulting oil was taken into CH2Cl2 and the organic layer was washed once with H2O, dried over K2CO3, and concentrated under reduced vacuum to yield 159 mg as a semi-solid. This material was purified via silica gel chromatography employing the Chromatotron and using a 2000 micron rotor while eluting with a solvent of methylene chloride/ethyl acetate 1:1 to yield the title compound (51 mg, 32%) as a white solid. Ion spray M.S. 393.1 (M*+1).

1. stirringThe reaction was stirred one hour at this temperature
2. concentrationconcentrated under reduced vacuum
3. customto yield a white semi-solid
4. stirringthe mixture was stirred overnight
5. concentrationIn the morning, the solution was concentrated under reduced vacuum
6. washthe organic layer was washed once with H2O
7. dry with materialdried over K2CO3
8. concentrationconcentrated under reduced vacuum
9. customto yield 159 mg as a semi-solid
10. customThis material was purified via silica gel chromatography
11. washwhile eluting with a solvent of methylene chloride/ethyl acetate 1:1