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(Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide

Base Information
  • Chemical Name:(Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide
  • CAS No.:1367282-60-7
  • Molecular Formula:C26H21Cl2F4N3O3
  • Molecular Weight:570.371
  • Hs Code.:
(Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide

Synonyms:(Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide

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Chemical Property of (Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide
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Technology Process of (Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide

There total 12 articles about (Z)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-(isopropoxyimino)ethyl)-1-naphthamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 9 steps
1.1: sodium hydrogencarbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / ethanol; water; toluene / 3 h / Reflux
2.1: ozone / methanol; dichloromethane / -78 °C
3.1: hydroxylamine hydrochloride / ethanol; water / 18 h / 45 °C
4.1: N-chloro-succinimide / N,N-dimethyl-formamide / 3.17 h / 20 °C
5.1: potassium hydrogencarbonate / ethyl acetate / 18 h / 20 °C
6.1: lithium hydroxide / 1,4-dioxane; water / 3 h / 20 °C
7.1: triethylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 20 °C
7.2: 2 h / 20 °C
8.1: Dess-Martin periodane / ethyl acetate / 2 h / 20 °C
9.1: potassium acetate / ethanol; water / 0.42 h / 130 °C / Microwave irradiation
With N-chloro-succinimide; hydroxylamine hydrochloride; potassium acetate; sodium hydrogencarbonate; potassium hydrogencarbonate; Dess-Martin periodane; ozone; triethylamine; HATU; lithium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 10 steps
1.1: sulfuric acid / 18 h / Reflux
2.1: sodium hydrogencarbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / ethanol; water; toluene / 3 h / Reflux
3.1: ozone / methanol; dichloromethane / -78 °C
4.1: hydroxylamine hydrochloride / ethanol; water / 18 h / 45 °C
5.1: N-chloro-succinimide / N,N-dimethyl-formamide / 3.17 h / 20 °C
6.1: potassium hydrogencarbonate / ethyl acetate / 18 h / 20 °C
7.1: lithium hydroxide / 1,4-dioxane; water / 3 h / 20 °C
8.1: triethylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 20 °C
8.2: 2 h / 20 °C
9.1: Dess-Martin periodane / ethyl acetate / 2 h / 20 °C
10.1: potassium acetate / ethanol; water / 0.42 h / 130 °C / Microwave irradiation
With N-chloro-succinimide; sulfuric acid; hydroxylamine hydrochloride; potassium acetate; sodium hydrogencarbonate; potassium hydrogencarbonate; Dess-Martin periodane; ozone; triethylamine; HATU; lithium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;
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