تفاعل #47392
ord-56eb754100494575bda9ce0e9605ac1c
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGThe mixture was stirred at room temperature for 4 h
- 2أخرىthe solvents were evaporated
- 3workup.ADDITIONThe residue was treated with ethyl acetate and ammonium chloride solution
- 4أخرىthe organic layer separated
- 5غسيلThe organic layer was washed with brine
- 6تجفيفdried over sodium sulfate
- 7أخرىThe solvents were evaporated
- 8أخرىthe residue was purified by ISCO flash chromatography (Teledyne Isco RediSep Flash Column 40 g, 10% to 80% ethyl acetate/hexanes) which
الإجراء التجريبي
To a solution of (S)-2-[4-(3-ethoxy-2-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid (prepared as in Example 114, 570 mg, 1.62 mmol) in N,N-dimethylformamide (10 mL) was added 1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl-methyl)-1H-pyrazol-3-ylamine (prepared as in Example 49, 382 mg, 1.94 mmol) and benzotriazol-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate (1.43 g, 3.23 mmol). The mixture was stirred at 0° C. and N,N-diisopropylethylamine (0.417 g, 3.23 mmol) was added. The mixture was stirred at room temperature for 4 h and the solvents were evaporated. The residue was treated with ethyl acetate and ammonium chloride solution, and the organic layer separated. The organic layer was washed with brine and dried over sodium sulfate. The solvents were evaporated and the residue was purified by ISCO flash chromatography (Teledyne Isco RediSep Flash Column 40 g, 10% to 80% ethyl acetate/hexanes) which afforded (S)-2-[4-(3-ethoxy-2-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid [1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl-methyl)-1H-pyrazol-3-yl]-amide (0.750 g, 87%) as a white solid.