Reacción #2146687
ord-9479d13a8d1746ebbe026f8062d709fe
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroto remove moisture
- 2workup.DISSOLUTIONwas dissolved in 10 L of N,N-dimethylformamide
- 3OtroAfter the completion of the reaction
- 4Extracciónextracted three times with chloroform
- 5LavadoThe combined chloroform layer was washed once with water and once with a saturated sodium chloride solution
- 6Secadodried over anhydrous sodium sulfate
- 7Filtraciónfiltered
- 8Concentraciónconcentrated
- 9OtroThe resulting crude product was purified by recycle preparative HPLC (HPLC apparatus
Procedimiento
242 mg (corresponding to 1.0 mmol) of 2-(4′-hydroxyphenyl)-6-methoxyimidazo[1,2-a]pyridine that was sufficiently dried to remove moisture was dissolved in 10 L of N,N-dimethylformamide, and 418 mg (corresponding to 3.0 mmol) of potassium carbonate was added thereto. The mixture was supplemented with 140 μL (corresponding to 1.5 mmol) of 1-bromo-3-fluoropropane, and then was stirred at room temperature for 18 hours. After the completion of the reaction, the reaction solution was poured into water and extracted three times with chloroform. The combined chloroform layer was washed once with water and once with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated. The resulting crude product was purified by recycle preparative HPLC (HPLC apparatus: LC-908 (under trade name: manufactured by Japan Analytical Industry Co., Ltd.); column: two JAIGEL 2H (under trade name; manufactured by Japan Analytical Industry Co., Ltd.) connected together; mobile phase: chloroform), to obtain 189 mg (corresponding to 0.63 mmol) of 2-[4′-(3″-fluoropropoxy)phenyl]-6-methoxyimidazo[1,2-a]pyridine (hereinafter referred to as Compound 1) (FIG. 2, Step 6).