تفاعل #316550

ord-cda5da00753d473fb6214fba7a966330

معادلة التفاعل

CCNC(=O)Nc1cn2ccc(-c3nc(C)n[nH]3)cc2n1
nitrile
CCNC(=O)Nc1cn2ccc(-c3nc(C)n[nH]3)cc2n1
1-ethyl-3-[7-(5-methyl-2H-[1,2,4]triazol-3-yl)-imidazo[1,2-a]pyridin-2-yl]-urea
NC(=O)C(F)(F)F
trifluoroacetamide
C=CC(=O)N(C)C
dimethylaminoacrolein
CCNC(=O)Nc1cn2ccc(-c3nc(C)n(C)n3)cc2n1
pyrimidine
CCNC(=O)Nc1cn2ccc(-c3nc(C)n(C)n3)cc2n1
1-[7-(1,5-dimethyl-1H-[1,2,4]triazol-3-yl)-imidazo[1,2-a]pyridin-2-yl]-3-ethyl-urea

المذيبات

ظروف التفاعل

درجة الحرارة
125°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction was then evaporated in vacuo
  2. 2
    أخرىthe residue was purified by silica gel chromatography (gradient elution: 0-20% ethyl acetate/dichloromethane)

الإجراء التجريبي

A mixture of nitrile 4 (0.500 g, 1.7 mmol), 0.50 g trifluoroacetamide and 0.25 g dimethylaminoacrolein in 5 mL ethanol was heated to 125° C. for 2 h by microwave irradiation (CEM, 300 watt). The reaction was then evaporated in vacuo and the residue was purified by silica gel chromatography (gradient elution: 0-20% ethyl acetate/dichloromethane) to give pyrimidine 5.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07563788B2uspto-grants-2009_07