반응 #534220

반응 방정식

1-(7-iodo-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea

4-(6-tributylstannanyl-pyridin-2-yl)-morpholine

→

title compound

수율 6.2%

1-Ethyl-3-[7-(6-morpholin-4-yl-pyridin-2-yl)-5-pyridin-3-yl-benzothiazol-2-yl]-urea

수율 6.2%

용매

DMF

반응 조건

후처리

1. 1
   기타The reaction mixture was then degassed for half an hour
2. 2
   기타The reaction mixture was then again degassed for half an hour
3. 3
   기타After the completion of the reaction (TLC monitoring), DMF
4. 4
   workup.DISTILLATIONwas distilled off
5. 5
   workup.ADDITIONwater was added to the reaction mixture
6. 6
   추출extracted with ethyl acetate
7. 7
   건조The combined organic layers were dried over anhydrous Na2SO4
8. 8
   기타evaporated to dryness under reduced pressure
9. 9
   기타The crude residue was purified by prep HPLC

실험 절차

To a solution of 1-(7-iodo-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea (0.15 g, 0.35 mmol) in DMF (5 mL) was added 4-(6-tributylstannanyl-pyridin-2-yl)-morpholine (0.30 g, 0.70 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) (0.020 g, 0.018 mmol). The reaction mixture was then again degassed for half an hour and heated at 120° C. for 15 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 by prep HPLC to get the title compound (0.01 g, 6.0%) as white solid.

출처