4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

Base Information

Chemical Name:4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester
CAS No.:1343455-54-8
Molecular Formula:C₁₆H₁₃BrFNO₂
Molecular Weight:350.187
Hs Code.:

Synonyms:4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

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Chemical Property of 4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

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Technology Process of 4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

There total 1 articles about 4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester 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:

Reference yield: 64.0%

: 188813-02-7
3-bromo-5-fluorobenzaldehyde

: 94-09-7
p-aminoethylbenzoate

: 1343455-54-8
4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

Guidance literature:: In ethanol; for 2h; Reflux;

Reference yield: 86.0%

: 1343455-54-8
4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

: 78-84-2
isobutyraldehyde

: 1343455-56-0
2-(3-bromo-5-fluoro-phenyl)-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester

Guidance literature:: With water; ytterbium(III) trifluoromethanesulfonate hydrate; In tetrahydrofuran; at 25 ℃; for 5h;

Reference yield:

: 1343455-54-8
4-{[1-(3-bromo-5-fluoro-phenyl)-methylidene]-amino}-benzoic acid ethyl ester

: 1343455-52-6
N-[2-(4'-tert-butyl-5-fluoro-biphenyl-3-yl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonyl]-methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: water / ytterbium(III) trifluoromethanesulfonate hydrate / tetrahydrofuran / 5 h / 25 °C

2: trifluoroacetic acid; triethylsilane / 1 h / 25 °C

3: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / 3 h / 120 °C

4: sodium hydroxide; water / ethanol; tetrahydrofuran / 12 h / 60 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dmap / dichloromethane / 12 h / Reflux

With triethylsilane; water; sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; sodium hydroxide; dmap; bis-triphenylphosphine-palladium(II) chloride; ytterbium(III) trifluoromethanesulfonate hydrate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; 1: Diels-Alder Reaction / 3: Suzuki Coupling;