Reacción #52073

Ecuación de reacción

2-(4-{[(3-carboxymethoxy-benzyl)-(pyridine-3-sulfonyl)-amino]-methyl}-phenyl)-2-methyl-propionic acid ethyl ester

LiOH.H2O

LiOH.H2O

→

title compound

Rendimiento 94.5%

2-(4-{[(3-Carboxymethoxy-benzyl)-(pyridine-3-sulfonyl)-amino]-methyl}-phenyl)-2-methyl-propionic acid

Rendimiento 94.5%

Disolventes

THF

water

water

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaThe reaction was heated
2. 2
   Temperaturaat reflux for 24 h
3. 3
   Temperaturathe reaction was heated
4. 4
   Temperaturaat reflux for 30 h
5. 5
   ConcentraciónThe mixture was concentrated in vacuo and to the residue
6. 6
   workup.ADDITIONwas added THF (3 mL) and water (1.5 mL)
7. 7
   TemperaturaThe reaction was heated
8. 8
   Temperaturaat reflux for 24 h
9. 9
   workup.ADDITIONThe solution was diluted with water
10. 10
    workup.ADDITIONthe pH was adjusted to about 5 by addition of 1N HCl
11. 11
    workup.ADDITIONSodium chloride was added
12. 12
    Lavadothe aqueous solution was washed with EtOAc (3×)
13. 13
    SecadoThe combined organic solutions were dried (MgSO4)
14. 14
    Filtraciónfiltered
15. 15
    Concentraciónconcentrated

Procedimiento

To a solution of 2-(4-{[(3-carboxymethoxy-benzyl)-(pyridine-3-sulfonyl)-amino]-methyl}-phenyl)-2-methyl-propionic acid ethyl ester (83 mg, 0.157 mmol) in THF (10 mL) was added water (1 mL) and LiOH.H2O (66 mg, 1.58 mmol). The reaction was heated at reflux for 24 h. Additional LiOH.H2O (66 mg, 1.58 mmol) in water (2 mL) was added and the reaction was heated at reflux for 30 h. The mixture was concentrated in vacuo and to the residue was added THF (3 mL) and water (1.5 mL). The reaction was heated at reflux for 24 h and was cooled to room temperature. The solution was diluted with water and the pH was adjusted to about 5 by addition of 1N HCl. Sodium chloride was added and the aqueous solution was washed with EtOAc (3×). The combined organic solutions were dried (MgSO4), filtered, and concentrated to provide the title compound (74 mg). 1H NMR (400 MHz, CDCl3) δ 8.94 (s, 1H), 8.73 (s, 1H), 8.13 (d, 1H), 7.55 (m, 1H), 7.23 (d, 2H), 7.11 (m, 3H), 6.78 (d, 1H), 6.73 (d, 1H), 6.68 (s, 1H), 4.90 (s, 2H), 4.39 (s, 2H), 3.30 (s, 2H), 1.50 (s, 6H); MS 497 (M−1).

Fuente