تفاعل #433599

معادلة التفاعل

Sodium

3-(4-morpholinyl)-1-propanol

4-[(3,4-dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazoline

→

4-[(3,4-dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline

المردود 72.0%

المذيبات

THF

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةThe reaction mixture was refluxed for 18 hours
2. 2
   أخرىthe solvent was thereafter partially removed under reduced pressure
3. 3
   workup.ADDITIONthe residue was diluted with water
4. 4
   استخلاصextracted with ethyl acetate
5. 5
   أخرىDrying
6. 6
   أخرىthe combined organic extracts, evaporation and silica gel chromatography (
7. 7
   workup.ADDITIONa mixture of 20% MeOH/30% CH2Cl2/50% EtOAc
8. 8
   غسيلas elute)

الإجراء التجريبي

Sodium metal (5 equivalents) was added, under nitrogen atmosphere, to a solution of 3-(4-morpholinyl)-1-propanol (4 equivalents) in THF. The obtained suspension was stirred at 20° C. for two hours and was thereafter cannulated, under nitrogen atmosphere, into a solution of 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazoline. The reaction mixture was refluxed for 18 hours, the solvent was thereafter partially removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate. Drying the combined organic extracts, evaporation and silica gel chromatography (using a mixture of 20% MeOH/30% CH2Cl2/50% EtOAc as elute) gave 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline in 72% yield.

المصدر