تفاعل #2146694
ord-b5a44cd795b54272b4de73317c71bf2c
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةThen, the mixture was refluxed for 23 hours
- 2درجة الحرارةAfter the reaction solution was cooled
- 3استخلاصextracted twice by a salting-out extraction procedure
- 4workup.ADDITIONwith addition of sodium chloride
- 5تجفيفThe combined chloroform layer was dried over anhydrous magnesium sulfate
- 6أخرىThe resulting crude product was purified by silica gel column chromatography (elution solvent: chloroform/methanol=10/1)
الإجراء التجريبي
1.18 g (corresponding to 3.57 mmol) of 2-[4′-(3″-fluoropropoxy)phenyl]-6-methoxymethoxyimidazo[1,2-a]pyridine was dissolved in 29 mL of isopropyl alcohol, and 0.59 mL of conc. hydrochloric acid was added thereto. Then, the mixture was refluxed for 23 hours. After the reaction solution was cooled, the solution was poured into water, and extracted twice by a salting-out extraction procedure using chloroform with addition of sodium chloride. The combined chloroform layer was dried over anhydrous magnesium sulfate. The resulting crude product was purified by silica gel column chromatography (elution solvent: chloroform/methanol=10/1), to obtain 481 mg (corresponding to 1.68 mmol) of 2-[4′-(3″-fluoropropoxy)phenyl]-6-hydroxyimidazo[1,2-a]pyridine (hereinafter referred to as Compound 2) (FIG. 3, Step 10).