反应详情

A 20 mL vial containing 3-((1-((benzyloxy)carbonyl)piperidin-4-yl)oxy)-5-chloro -2-methylbenzoic acid (35.0 mg, 0.087 mmol) was charged with 3-(aminomethyl)-2,6-dimethylpyridin-4(1H)-one hydrochloride (17.98 mg, 0.095 mmol), EDC (24.92 mg, 0.130 mmol), HOAt (20.04 mg, 0.130 mmol), N,N-dimethylformamide (1 mL), N-methylmorpholine (0.143 mL, 1.300 mmol) and a magnetic stir bar. The vial was capped and the reaction was stirred at room temperature for 3 days, at which time it was dripped into a stirred solution of saturated NaHCO3 (20 mL) and water (5 mL). The suspension was stirred at room temperature for 20 min and the solid was collected via vacuum filtration and dried under high vacuum. Purification of the solid by reverse phase HPLC (Column: Phenomenex Gemini-NX axia, 30×100, 5μ, C18. Eluent:10-80% acetonitrile/0.1% formic acid in water, 7 min gradient) gave benzyl 4-(5-chloro-3-(((2,6-dimethyl-4-oxo-1,4-dihydropyridin-3-yl)methyl)carbamoyl)-2-methylphenoxy)piperidine-1-carboxylate (30 mg, 0.056 mmol, 64.3% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 8.21 (t, J=5.05 Hz, 1H), 7.26-7.44 (m, 5H), 7.15 (d, J=2.02 Hz, 1H), 6.81 (d, J=2.02 Hz, 1H), 5.87 (s, 1H), 5.09 (s, 2H), 4.70 (br. s., 1H), 4.19 (d, J=5.05 Hz, 2H), 3.63 (br. s., 2H), 3.36-3.45 (m, 2H), 2.31 (s, 3H), 2.15 (s, 3H), 2.06 (s, 3H), 1.90 (d, J=12.88 Hz, 2H), 1.49-1.67 (m, 2H). MS(ES) [M+H]+ 538.3.

1. customThe vial was capped
2. stirringThe suspension was stirred at room temperature for 20 min
3. filtrationthe solid was collected via vacuum filtration
4. customdried under high vacuum
5. customPurification of the solid by reverse phase HPLC (Column: Phenomenex Gemini-NX axia, 30×100, 5μ, C18. Eluent:10-80% acetonitrile/0.1% formic acid in water, 7 min gradient)