تفاعل #2254229

ord-30c908eabd58484d80342a4089d2aedc

معادلة التفاعل

CCOC(=O)C=CC(OC)OC
4,4-dimethoxy-but-2-enoic acid ethyl ester
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
Nc1ccccn1
2-aminopyridine
CCOC(=O)Cc1cnc2ccccn12
desired compound
المردود 73.4%
CCOC(=O)Cc1cnc2ccccn12
Imidazo[1,2-α]pyridin-3-yl-acetic acid ethyl ester
المردود 73.4%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةHeat
  2. 2
    درجة الحرارةat reflux for 2 hours
  3. 3
    درجة الحرارةHeat the mixture
  4. 4
    درجة الحرارةat reflux for 16 hours
  5. 5
    درجة الحرارةthen cool to room temperature
  6. 6
    غسيلwash sequentially with saturated aqueous sodium bicarbonate (600 mL×3) and saturated aqueous sodium chloride (600 mL×2)
  7. 7
    تجفيفDry the organic phase over sodium sulfate
  8. 8
    تركيزconcentrate under reduced pressure

الإجراء التجريبي

Heat a mixture of 4,4-dimethoxy-but-2-enoic acid ethyl ester (43.5 g, 250 mmol) and p-toluenesulfonic acid (4.75 g, 25 mmol) in acetonitrile (240 mL) and water (15 mL) at reflux for 2 hours. Cool the reaction mixture to room temperature and add 2-aminopyridine (18.8 g, 200 mmol). Heat the mixture at reflux for 16 hours then cool to room temperature. Dilute the reaction mixture with ethyl acetate (1200 mL) and wash sequentially with saturated aqueous sodium bicarbonate (600 mL×3) and saturated aqueous sodium chloride (600 mL×2). Dry the organic phase over sodium sulfate and concentrate under reduced pressure to provide the desired compound as a brown oil (30 g, 73%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09044487B2uspto-grants-2015_06