تفاعل #1685102
ord-be2757e016e94b7a9b39b69f0430674d
معادلة التفاعل
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةThe mixture was refluxed for 16 hours under an atmosphere of dry N2(g)
- 2أخرىthe solvent was removed in vacuo
- 3أخرىThe residue was partitioned between CHCl3 and 1M NaOH
- 4غسيلthe organic phase was washed with brine
- 5تجفيفdried over Na2SO4(g)
- 6تركيزconcentrated in vacuo
- 7أخرىThe residue (535 mg) was purified by flash chromatography on silica using 80%EtOAc/CH2 Cl2
الإجراء التجريبي
To 6-fluoroindoline (274 mg, 2.0 mmol) in dry i-PrOH (10mL) was added 4-chloro-6,7-dimethoxy-quinazoline (225 mg, 1.0 mmol). The mixture was refluxed for 16 hours under an atmosphere of dry N2(g) and then the solvent was removed in vacuo. The residue was partitioned between CHCl3 and 1M NaOH, and the organic phase was washed with brine, dried over Na2SO4(g) and concentrated in vacuo. The residue (535 mg) was purified by flash chromatography on silica using 80%EtOAc/CH2 Cl2 to yield 4-(6-fluoro-2,3-dihydro-indol-1-yl)-6,7-dimethoxyquinazoline as its free base (293 mg) (GC/MS: 325 (M+); LC-MS: 326 (MH+); anal. RP18-HPLC RT: 4.37 min.).