تفاعل #69645

ord-52d15fc4d6fc4139af8d6f37a462d641

ظروف التفاعل

درجة الحرارة
145°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was refluxed
  2. 2
    درجة الحرارةcooled
  3. 3
    ترشيحfiltered
  4. 4
    أخرىThe filtrate was evaporated
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in CH2Cl2
  6. 6
    غسيلwashed with 1 N NaOH
  7. 7
    ترشيحfiltered
  8. 8
    workup.DISSOLUTIONThe solid was dissolved in 2-propanone
  9. 9
    أخرىevaporated onto silica gel
  10. 10
    أخرىchromatographed
  11. 11
    أخرىThe pure fractions were collected
  12. 12
    أخرىthe solvent was evaporated

الإجراء التجريبي

To a flask under Argon was added 4-amino-2,5,6-trichloropyrimidine (0.08564 mol), 4-amino-benzonitrile (0.1071 mol), 1-methyl-2-pyrrolidinone (17 ml) and HCl in diethylether (1M; 85.6 ml). The mixture was placed in an oil bath at 130° C. under a stream of nitrogen until the ether was gone. An additional 10 ml of 1-methyl-2-pyrrolidinone was added. The mixture was heated at 145° C. for 16 hours under argon. 1,4-Dioxane was added. The mixture was refluxed, cooled, then filtered. The filtrate was evaporated. The residue was dissolved in CH2Cl2, washed with 1 N NaOH, then filtered. The solid was dissolved in 2-propanone, evaporated onto silica gel, and chromatographed using 1-3% 2-propanone in hexane as eluent. The pure fractions were collected and the solvent was evaporated, yielding 1.63 g (6.8%) of 4-[(4-amino-5,6-dichloro-2-pyrimidinyl)amino]benzonitrile (interm. 12).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530655B2uspto-grants-2013_09