Reacción #1005942

ord-02445459c6a74033bffeb3cffd807533

Ecuación de reacción

CO/N=C(\C=C(\C)COc1ccn(-c2ccc(Cl)cc2)n1)C(=O)OC
methyl(Z,2E)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-4-methyl-pent-3-enoate
CN
methylamine
CNC(=O)C(C=C(C)COc1ccn(-c2ccc(Cl)cc2)n1)=NOC
5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-N,4-dimethyl-pent-3-enamide

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITwas continued over night
  2. 2
    OtroAfter removal of the solvent in vacuo the mixture
  3. 3
    Otrowas purified by chromatography on silica with a heptane/ethyl acetate gradient
  4. 4
    Otro90 mg of the desired Z-isomer have been collected

Procedimiento

0.68 g (1.87 mmol) methyl(Z,2E)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-4-methyl-pent-3-enoate and E-isomer from the previous reaction have been dissolved in 3.0 ml THF. 2.0 ml 40% aqueous methylamine have been added at ambient temperature with stirring which was continued over night. After removal of the solvent in vacuo the mixture was purified by chromatography on silica with a heptane/ethyl acetate gradient. 90 mg of the desired Z-isomer have been collected. 1H-NMR (CDCl3): δ=2.03 (s); 2.85 (d); 3.97 (s); 4.64 (s); 5.87 (s); 6.02 (d); 6.65 (br); 7.35 (d); 7.50 (d); 7.67 (d).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09271501B2uspto-grants-2016_03