(2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

Base Information

Chemical Name:(2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid
CAS No.:1402555-12-7
Molecular Formula:C₂₃H₃₀FNO₅
Molecular Weight:419.493
Hs Code.:

Synonyms:(2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

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Chemical Property of (2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

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Technology Process of (2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

There total 14 articles about (2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)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:

: 68886-07-7
(2-fluoro-4-hydroxylphenyl)acetic acid

: 1402555-12-7
(2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid

2: triphenylphosphine; di-tert-butyl-diazodicarboxylate / dichloromethane / 3 h / 20 °C

3: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C

With di-tert-butyl-diazodicarboxylate; water; triphenylphosphine; lithium hydroxide; sulfuric acid; In tetrahydrofuran; methanol; dichloromethane;

Reference yield:

: 1402555-11-6
1-methylcyclopropyl 4-[(1R,2S)-2-{2-[3-fluoro-4-(2-methoxy-2-oxoethyl)phenoxy]ethyl}cyclopropyl]piperidine-1-carboxylate

: 1402555-12-7
(2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

Guidance literature:: 1-methylcyclopropyl 4-[(1R,2S)-2-{2-[3-fluoro-4-(2-methoxy-2-oxoethyl)phenoxy]ethyl}cyclopropyl]piperidine-1-carboxylate; With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃;

With hydrogenchloride; In water;

Reference yield:

: 287192-97-6
4-ethynyl-piperidine-1-carboxylic acid tert-butyl ester

: 1402555-12-7
(2-fluoro-4-{2-[(1S,2R)-2-( 1-{[(1-methylcyclopropyl)oxy]carbonyl} piperidin-4-yI)cyclopropyl]ethoxy}phenyl)acetic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 0.08 h / -78 °C

1.2: 1 h / -78 °C

2.1: hydrogen; quinoline / Lindlars catalyst / ethyl acetate / 0.67 h

3.1: diethylzinc / dichloromethane; diethyl ether / 0.17 h / -20 °C / Inert atmosphere

3.2: 0.17 h

3.3: 24 h / 0 °C

4.1: hydrogen / palladium(II) hydroxide / ethyl acetate; ethanol / 2585.81 Torr

4.2: 0 °C

4.3: 0.5 h / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

6.1: triethylamine / dichloromethane / 0.5 h / 20 °C

7.1: triphenylphosphine; di-tert-butyl-diazodicarboxylate / dichloromethane / 3 h / 20 °C

8.1: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C

With quinoline; hydrogenchloride; n-butyllithium; di-tert-butyl-diazodicarboxylate; water; hydrogen; diethylzinc; triethylamine; triphenylphosphine; lithium hydroxide; palladium(II) hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; hexane; dichloromethane; ethyl acetate;