Reaktion #165482

Reaktionsgleichung

4-chloro-N-methyl-2-pyridinecarboxamide

K2CO3

4-aminophenol

potassium tert-butoxide

→

4-(2-(N-methylcarbamoyl)-4-pyridyloxy)aniline

Ausbeute 84.0%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe mixture was cooled to room temp.
2. 2
   Sonstigeseparated between EtOAc (500 mL)
3. 3
   ExtraktionThe aqueous phase was back-extracted with EtOAc (300 mL)
4. 4
   WaschenThe combined organic layers were washed with a saturated NaCl solution (4×1000 mL)
5. 5
   Trocknendried (Na2SO4)
6. 6
   Einengenconcentrated under reduced pressure
7. 7
   SonstigeThe resulting solids were dried under reduced pressure at 35° C. for 3 h

Vorschrift

A solution of 4-aminophenol (9.60 g, 88.0 mmol) in anh. DMF (150 mL) was treated with potassium tert-butoxide (10.29 g, 91.7 mmol), and the reddish-brown mixture was stirred at room temp. for 2 h. The contents were treated with 4-chloro-N-methyl-2-pyridinecarboxamide (15.0 g, 87.9 mmol) and K2CO3 (6.50 g, 47.0 mmol) and then heated at 80° C. for 8 h. The mixture was cooled to room temp. and separated between EtOAc (500 mL) and a saturated NaCl solution (500 mL). The aqueous phase was back-extracted with EtOAc (300 mL). The combined organic layers were washed with a saturated NaCl solution (4×1000 mL), dried (Na2SO4) and concentrated under reduced pressure. The resulting solids were dried under reduced pressure at 35° C. for 3 h to afford 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)aniline as a light-brown solid 17.9 g, 84%): 1H-NMR (DMSO-d6) δ 2.77 (d, J=4.8 Hz, 3H), 5.17 (br s, 2H), 6.64, 6.86 (AA′BB′ quartet, J=8.4 Hz, 4H), 7.06 (dd, J=5.5, 2.5 Hz, 1H), 7.33 (d, J=2.5 Hz, 1H), 8.44 (d, J=5.5 Hz, 1H), 8.73 (br d, 1H); HPLC ES-MS m/z 244 ((M+H)+).

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