(2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

Base Information

Chemical Name:(2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid
CAS No.:1141473-38-2
Molecular Formula:C₂₅H₂₁FN₂O₅
Molecular Weight:448.451
Hs Code.:

Synonyms:(2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

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Chemical Property of (2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

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Technology Process of (2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

There total 10 articles about (2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid 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: 95.0%

: 1141475-76-4
tert-butyl (2-fluoro-4-{5-[2-(methoxymethyl)-2'-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetate

: 1141473-38-2
(2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 16h;
DOI:10.1002/cmdc.201402557

Reference yield:

: 148547-19-7
4-Bromo-3-methylbenzoic acid methyl ester

: 1141473-38-2
(2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 7 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / chloroform / 48 h / 70 °C / Inert atmosphere

2: 96 h / Reflux

3: potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; toluene / 1 h / 110 °C / Inert atmosphere

4: sodium hydroxide / ethanol / 1 h / 60 °C

5: N-ethyl-N,N-diisopropylamine / 0 - 20 °C / Inert atmosphere

6: acetonitrile / 0.5 h / 150 °C / Microwave irradiation

7: hydrogenchloride / 1,4-dioxane / 16 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; 2,2'-azobis(isobutyronitrile); potassium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; ethanol; chloroform; water; toluene; acetonitrile;
DOI:10.1002/cmdc.201402557

Reference yield:

: 142031-67-2
methyl 4-bromo-3-(bromomethyl)benzoate

: 1141473-38-2
(2-fluoro-4-{5-[2-(methoxymethyl)-2’-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 96 h / Reflux

2: potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; toluene / 1 h / 110 °C / Inert atmosphere

3: sodium hydroxide / ethanol / 1 h / 60 °C

4: N-ethyl-N,N-diisopropylamine / 0 - 20 °C / Inert atmosphere

5: acetonitrile / 0.5 h / 150 °C / Microwave irradiation

6: hydrogenchloride / 1,4-dioxane / 16 h / 20 °C

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; ethanol; water; toluene; acetonitrile;
DOI:10.1002/cmdc.201402557