تفاعل #534217
ord-ed28055f320c40dd85f0b9b9e7039ee6
معادلة التفاعل
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىThe reaction mixture was then degassed for half an hour
- 2أخرىThe reaction mixture was then again degassed
- 3أخرىAfter the completion of the reaction (TLC monitoring), DMF
- 4workup.DISTILLATIONwas distilled off
- 5workup.ADDITIONwater was added to the reaction mixture
- 6استخلاصextracted with ethyl acetate
- 7تجفيفThe combined organic layers were dried over anhydrous Na2SO4
- 8أخرىevaporated to dryness under reduced pressure
- 9أخرىThe crude residue was purified over silica gel (230-400 M)
الإجراء التجريبي
To a solution of 1-(5-bromo-7-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea (0.20 g, 0.53 mmol) in DMF (5 mL) was added 2-tributylstannyl pyridine (0.23 g, 0.53 mmol) under nitrogen atmosphere at room temperature. The reaction mixture was then degassed for half an hour followed by the addition of tetrakis(triphenylphosphine)palladium(0) (0.061 g, 0.053 mmol). The reaction mixture was then again degassed and heated at 120° C. for 8 h under nitrogen atmosphere. After the completion of the reaction (TLC monitoring), DMF was distilled off; water was added to the reaction mixture and extracted with ethyl acetate. The combined organic layers were dried over anhydrous Na2SO4, and evaporated to dryness under reduced pressure. The crude residue was purified over silica gel (230-400 M) using EtOAc-Hexane (80:20) to provide the title compound as off white solid (0.012 g, 6%).