반응 #1005942

ord-02445459c6a74033bffeb3cffd807533

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITwas continued over night
  2. 2
    기타After removal of the solvent in vacuo the mixture
  3. 3
    기타was purified by chromatography on silica with a heptane/ethyl acetate gradient
  4. 4
    기타90 mg of the desired Z-isomer have been collected

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09271501B2uspto-grants-2016_03