反応 #1005942

ord-02445459c6a74033bffeb3cffd807533

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITwas continued over night
  2. 2
    その他After removal of the solvent in vacuo the mixture
  3. 3
    その他was purified by chromatography on silica with a heptane/ethyl acetate gradient
  4. 4
    その他90 mg of the desired Z-isomer have been collected

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09271501B2uspto-grants-2016_03