تفاعل #2045085

ord-5f0e2d8db72e4e1cb105153ed5036e95

معادلة التفاعل

Cc1cncn1CCCN1C(=O)c2ccccc2C1=O
2-(3-(5-Methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione
Cc1cncn1CCCN
3-(5-Methyl-1H-imidazol-1-yl)propan-1-amine

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةunder reflux over night
  2. 2
    تركيزmixture was concentrated down to a volume of 25 mL
  3. 3
    workup.ADDITIONHydrochloric acid (conc., 55 mL) was then added
  4. 4
    ترشيحThe formed precipitate was then filtered
  5. 5
    درجة الحرارةThe filtrate was cooled to 0° C.
  6. 6
    workup.ADDITIONsolid NaOH was added until a final pH-value of 10-12
  7. 7
    استخلاصThe aqueous solution was extracted by means of CHCl3 (3×50 mL)
  8. 8
    تجفيفThe combined organic layers were dried over Na2SO4
  9. 9
    ترشيحfiltered
  10. 10
    أخرىthe solvent was removed
  11. 11
    أخرىThe product was purified by means of flash-chromatography

الإجراء التجريبي

2-(3-(5-Methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione (i.e. 8.92 mmol, 1 eq., which may be prepared as described in D3) and hydzine monohydrate (17.84 mmol, 2 eq.) were dissolved in dry EtOH (50 mL). The mixture was kept under reflux over night, then 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08409837B2uspto-grants-2013_04