تفاعل #2045086
ord-d24d5d01e990443182ae3880c38a1d56
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةunder reflux
- 2درجة الحرارةunder reflux over night
- 3تركيزthe mixture was concentrated down to a volume of 25 mL
- 4workup.ADDITIONHydrochloric acid (conc., 55 mL) was then added
- 5workup.WAITkept at this temperature for 30 min
- 6ترشيحThe formed precipitate was then filtered
- 7درجة الحرارةThe filtrate was cooled to 0° C.
- 8workup.ADDITIONsolid NaOH was added until a final pH-value of 10-12
- 9استخلاصThe aqueous solution was extracted by means of CHCl3 (3×50 mL)
- 10تجفيفThe combined organic layers were dried over Na2SO4
- 11ترشيحfiltered
- 12أخرىthe solvent was removed
- 13أخرىThe product was purified by means of flash-chromatography
- 14workup.ADDITIONa CHCl3/MeOH-gradient containing aqueous ammonia (2% v/v)
الإجراء التجريبي
2-(3-(4-Methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione (3.42 mmol, 1 eq., which may be prepared as described in D6) and hydrazine monohydrate (6.84 mmol, 2 eq.) were dissolved in 20 mL of ethanol and the mixture was stirred for 12 h under reflux. The mixture was kept under reflux over night, then the mixture was concentrated down to a volume of 25 mL. Hydrochloric acid (conc., 55 mL) was then added and the mixture was heated to 50° C. and kept at this temperature for 30 min. The formed precipitate was then filtered. The filtrate was cooled to 0° C. and solid NaOH was added until a final pH-value of 10-12 was reached. The aqueous solution was extracted by means of CHCl3 (3×50 mL). The combined organic layers were dried over Na2SO4, filtered and the solvent was removed. The product was purified by means of flash-chromatography using silica gel and a CHCl3/MeOH-gradient containing aqueous ammonia (2% v/v).