تفاعل #792213

ord-1298a6f452cc400ca0b63f7166fb57a9

معادلة التفاعل

[Cl-].[Na+]
sodium chloride
Brc1cccc(-c2ncccn2)n1
2-(6-bromopyridin-2-yl)pyrimidine
CC(C)NC(C)C
N-isopropylpropane-2-amine
C#C[Si](C)(C)C
ethynyl(trimethyl)silane
C[Si](C)(C)C#Cc1cccc(-c2ncccn2)n1
2-{6-[(Trimethylsilyl)ethynyl]pyridin-2-yl}pyrimidine

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىdegassed in an ultrasonic bath under argon
  2. 2
    ترشيحthe mixture was filtered through Celite
  3. 3
    استخلاصthe aqueous phase was extracted repeatedly with ethyl acetate
  4. 4
    تجفيفThe combined organic phases were dried over magnesium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated
  7. 7
    أخرىpurified chromatographically

الإجراء التجريبي

1.00 g (3.99 mmol) of 2-(6-bromopyridin-2-yl)pyrimidine, 45.5 mg (239 μmol) of copper(I) iodide and 670 μl (4.78 mmol) of N-isopropylpropane-2-amine were initially charged in 15 ml of tetrahydrofuran and degassed in an ultrasonic bath under argon. The reaction mixture was then heated to 50° C., 168 mg (239 mol) of dichloro[bis(triphenylphosphoranyl)]palladium were added and 1.70 ml (12.0 mmol) of ethynyl(trimethyl)silane were added dropwise over a period of one hour. The mixture was then stirred at 60° C. for a further two hours. For work-up, the mixture was added to semiconcentrated sodium chloride solution, the mixture was filtered through Celite and the aqueous phase was extracted repeatedly with ethyl acetate. The combined organic phases were dried over magnesium sulfate, filtered, concentrated and purified chromatographically. This gave 520 mg (51% of theory) of 2-{6-[(trimethylsilyl)ethynyl]pyridin-2-yl}pyrimidine.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09173396B2uspto-grants-2015_11