تفاعل #168863

ord-3d901db4a2d94b1cb0b910ff3494ed07

المذيبات

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction liquid
  2. 2
    ترشيحwas filtered
  3. 3
    استخلاصextracted with chloroform
  4. 4
    غسيلthe combined organic layers were washed with water
  5. 5
    تجفيفa saturated saline solution and dried over anhydrous sodium sulfate
  6. 6
    تركيزby being concentrated under reduced pressure
  7. 7
    workup.DISSOLUTIONThe resultant residue was dissolved in ammonia water (1 ml)
  8. 8
    workup.STIRRINGmethanol (4 ml), and the solution was stirred at 50° C. for 2 hours
  9. 9
    درجة الحرارةThe reaction solution was cooled to room temperature
  10. 10
    تركيزconcentrated under reduced pressure
  11. 11
    أخرىthe precipitate was obtained through filtration
  12. 12
    غسيلwashed with ether
  13. 13
    أخرىdried

الإجراء التجريبي

To a solution of pyridin-2-amine (101 mg, 1.08 mmol) and 4-chloroquinazolin-6-ylacetate (200 mg, 0.90 mmol) in toluene (4 ml), tris(dibenzylideneacetone)dipalladium (0) (82.0 mg, 0.090 mmol), (±)BINAP (112.0 mg, 0.180 mmol) and cesium carbonate (585 mg, 1.80 mmol) were added, and the mixture was stirred under nitrogen atmosphere at 120° C. for 2 hours. The reaction liquid was filtered, followed by vacuum concentration of the filtrate. The residue was suspended in water and then extracted with chloroform, and thereafter the combined organic layers were washed with water and a saturated saline solution and dried over anhydrous sodium sulfate, followed by being concentrated under reduced pressure. The resultant residue was dissolved in ammonia water (1 ml) and methanol (4 ml), and the solution was stirred at 50° C. for 2 hours. The reaction solution was cooled to room temperature and then concentrated under reduced pressure, the resultant residue was suspended in ether, and the precipitate was obtained through filtration, washed with ether and then dried to give 4-(pyridin-2-ylamino)quinazolin-6-ol (138 mg, yield: 64%) as a brown solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846700B2uspto-grants-2014_09