Reacción #494391

Ecuación de reacción

sodium borohydride

sodium azide

Methyl 4,6-dichloro-3-methoxypicolinate

EtOAc

→

desired product

Rendimiento 33.0%

methyl 4-amino-6-chloro-3-methoxypicolinate

Rendimiento 33.0%

Disolventes

H2O

N,N-dimethylformamide

H2O

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaAfter cooling
2. 2
   LavadoThe organic phase was washed with H2O (2×10 mL)
3. 3
   Secadodried (Na2SO4)
4. 4
   Otroevaporated
5. 5
   workup.DISSOLUTIONThis material was dissolved in methyl alcohol (CH3OH; 15 mL)
6. 6
   Otrothe volatiles were removed under vacuum
7. 7
   Lavadowashed with H2O (10 mL)
8. 8
   Secadodried (Na2SO4)
9. 9
   Otroevaporated

Procedimiento

Methyl 4,6-dichloro-3-methoxypicolinate (320 mg, 1.4 mmol) was dissolved in dry N,N-dimethylformamide (DMF; 5 mL), treated with sodium azide (130 mg, 2.0 mmol) and heated at 50° C. for 5 h. After cooling, the mixture was shaken with EtOAc (20 mL) and H2O (10 mL). The organic phase was washed with H2O (2×10 mL) and satd aq NaCl (1×10 mL), dried (Na2SO4) and evaporated. This material was dissolved in methyl alcohol (CH3OH; 15 mL), treated with sodium borohydride (NaBH4; 55 mg, 1.4 mmol) and stirred at 20° C. for 1 h. The mixture was treated with H2O (10 mL), and the volatiles were removed under vacuum. The residue was taken up in EtOAc (25 mL), washed with H2O (10 mL) and satd aq sodium chloride (NaCl; 10 mL), dried (Na2SO4), and evaporated to give the desired product as a white solid (100 mg, 33%): mp 78-79° C.; 1H NMR (400 MHz, CDCl3) δ 6.76 (s, 1H), 4.84 (s, 2H), 3.95 (s, 3H), 3.87 (s, 3H); EIMS m/z 216.

Fuente