Reacción #1994304

ord-841e96a94c6740dd945dcd91b575c408

Ecuación de reacción

CCOC(=O)/C(N)=C/C(=O)/C=C/c1ccc(Cl)cc1F
(2Z,5E)-2-amino-6-(4-chloro-2-fluoro-phenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester
CCOC(=O)/C(N)=C/C(=O)/C=C/c1ccc(Cl)cc1F
(2Z,5E)-2-amino-6-(4-chloro-2-fluorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester
CCOC(=O)C1=CC(=O)CC(c2ccc(Cl)cc2F)N1
6-(4-chloro-2-fluorophenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylic acid ethyl ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrogave
  2. 2
    Otropurification by silica gel chromatography
  3. 3
    Lavadoeluting with 40% EtOAc/hexanes, 6-(4-chloro-2-fluorophenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylic acid ethyl ester (11; 43 g, 49%, 96% pure by HPLC) as a tan solid

Procedimiento

Using the procedure of Example 5, (2Z,5E)-2-amino-6-(4-chloro-2-fluoro-phenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester (7; 88 g, 0.296 mol) in 1,4-dioxane (880 mL) in a 2 liter Parr reactor gave, following purification by silica gel chromatography eluting with 40% EtOAc/hexanes, 6-(4-chloro-2-fluorophenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylic acid ethyl ester (11; 43 g, 49%, 96% pure by HPLC) as a tan solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08598086B2uspto-grants-2013_12