Reaktion #51506

Reaktionsgleichung

sodium cyanoborohydride

HOAc

6-methoxy-5-formyl-2-naphthoic acid methyl ester

4-trifluoromethoxy-benzyl amine

→

product

Ausbeute 42.0%

6-Methoxy-5-({[4-(trifluoromethoxy)benzyl]amino}methyl)-2-naphthoic acid methyl ester

Ausbeute 42.0%

Lösungsmittel

EtOH

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigereaction
2. 2
   workup.WAITAfter 1 h at this temperature
3. 3
   Temperaturthe reaction was heated to 45° C. for 2 h
4. 4
   SonstigeThe solution was quenched with sat. aq. NaHCO3 (20 mL)
5. 5
   Extraktionextracted with EtOAc (200 mL)
6. 6
   WaschenThe organic layer was washed with brine (20 mL)
7. 7
   Trocknendried (MgSO4)
8. 8
   EinengenAfter concentration
9. 9
   Sonstigethe residue was purified by flash chromatography (0 to 10% MeOH:CHCl3 gradient)

Vorschrift

To a stirred solution of 6-methoxy-5-formyl-2-naphthoic acid methyl ester (1.09 g, 4.46 mmol) in EtOH (40 mL) at room temperature was added 4-trifluoromethoxy-benzyl amine (0.749 mL, 4.91 mmol) followed by HOAc (0.255 mL, 4.46 mmol). After 10 min. at this temperature, sodium cyanoborohydride (0.420 g, 6.69 mmol) was added, and reaction was continued stirring at rt for 4 h. After 1 h at this temperature, the reaction was heated to 45° C. for 2 h. The solution was quenched with sat. aq. NaHCO3 (20 mL) and then extracted with EtOAc (200 mL). The organic layer was washed with brine (20 mL) and dried (MgSO4). After concentration, the residue was purified by flash chromatography (0 to 10% MeOH:CHCl3 gradient) to afford the product (0.780 g, 42%) as a solid; 1H NMR (DMSO-d6) δ3.77 (s, 2H), 3.86 (s, 3H), 3.88 (s, 3H), 4.07 (s, 2H), 7.26 (d, J =8.0 Hz, 2H), 7.44 (d, J=8.6 Hz, 2H), 7.48 (d, J=9.2 Hz, 1H), 7.88 (dd, J=1.9, 8.9 Hz, 1H), 8.06 (d, J=5.2 Hz, 1H), 8.08 (d, J=5.3 Hz, 1H), 8.52 (d, J=1.7 Hz, 1H); mass spectrum [(+) El], m/z 420 (M+H)+.

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