تفاعل #69645
ord-52d15fc4d6fc4139af8d6f37a462d641
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةThe mixture was refluxed
- 2درجة الحرارةcooled
- 3ترشيحfiltered
- 4أخرىThe filtrate was evaporated
- 5workup.DISSOLUTIONThe residue was dissolved in CH2Cl2
- 6غسيلwashed with 1 N NaOH
- 7ترشيحfiltered
- 8workup.DISSOLUTIONThe solid was dissolved in 2-propanone
- 9أخرىevaporated onto silica gel
- 10أخرىchromatographed
- 11أخرىThe pure fractions were collected
- 12أخرىthe 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).