تفاعل #1685102

ord-be2757e016e94b7a9b39b69f0430674d

الكواشف

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المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was refluxed for 16 hours under an atmosphere of dry N2(g)
  2. 2
    أخرىthe solvent was removed in vacuo
  3. 3
    أخرىThe residue was partitioned between CHCl3 and 1M NaOH
  4. 4
    غسيلthe organic phase was washed with brine
  5. 5
    تجفيفdried over Na2SO4(g)
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe 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.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05736534uspto-grants-1998_04