تفاعل #7872

ord-640654338223404497e09faf1387ac75

الكواشف

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المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was concentrated in vacuo
  2. 2
    أخرىthe residue partitioned between EtOAc and H2O
  3. 3
    أخرىthe layers separated
  4. 4
    استخلاصextracted with EtOAc
  5. 5
    غسيلThe combined organic layers were washed with saturated NaHCO3 and brine
  6. 6
    تجفيفdried over MgSO4
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated in vacuo

الإجراء التجريبي

To a stirred solution of 3-aminopyridine (9.41 g, 100 mmol) and triethylamine (16.7 mL, 120 mmol) in CH2Cl2 (300 mL) at 0° C. was added trimethylacetyl chloride (14.8 mL, 120 mmol) dropwise over 15 min. The reaction was warmed to rt and stirred overnight. The mixture was concentrated in vacuo, the residue partitioned between EtOAc and H2O, and the layers separated. The aqueous layer was made basic with saturated NaHCO3 and extracted with EtOAc. The combined organic layers were washed with saturated NaHCO3 and brine, dried over MgSO4, filtered, and concentrated in vacuo to give N-(pyridin-3-yl)-2,2-dimethylpropanamide as a tan solid. 1H NMR (CDCl3, 300 MHz) δ 8.57 (d, 1H), 8.33 (dd, 1H), 8.17 (ddd, 1H), 7.69 (br s, 1H), 7.27 (dd, 1H), 1.33 (s, 9H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087601B2uspto-grants-2006_08