Reaktion #216787

ord-3032fccfcfdf489bb623754cf0a71015

Reaktionsgleichung

CCOCC
Ether
CCO
ethanol
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
O=C(O)c1ccc(I)nc1
6-iodo-nicotinic acid
CCOC(=O)c1ccc(I)nc1
title compound
CCOC(=O)c1ccc(I)nc1
Ethyl 6-Iodo-nicotinoate

Reaktionsbedingungen

Temperatur
55°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred at room temperature for 12 hours
  2. 2
    Sonstigethe layers separated
  3. 3
    ExtraktionThe aqueous layer was extracted with 2×40 ml of ether
  4. 4
    Waschenwashed with saturated NaCl
  5. 5
    Trocknendried over Na2SO4
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigeyielding a white solid which
  8. 8
    Sonstigewas purified by flash chromatography (SiO2, 10% ethyl acetate in hexanes)

Vorschrift

A mixture of 16.230 g (84.5 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride in 90 ml of methylene chloride was cannulated into a mixture of 17.80 g (71.2 mmol) of 6-iodo-nicotinic acid in 30 ml of methylene chloride. The resulting mixture was stirred and 7.85 g (0.171 mmol) of ethanol, and then 0.826 g (6.8 mmol) of 4-dimethylaminopyridine was added and the resulting mixture refluxed at 55° C. for 20 hours and then stirred at room temperature for 12 hours. Ether and water were added and the layers separated. The aqueous layer was extracted with 2×40 ml of ether and the organic portions combined, washed with saturated NaCl, dried over Na2SO4, and concentrated yielding a white solid which was purified by flash chromatography (SiO2, 10% ethyl acetate in hexanes) to give the title compound as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05468879uspto-grants-1995_11