{4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

Base Information

Chemical Name:{4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid
CAS No.:1402555-17-2
Molecular Formula:C₂₆H₂₉F₂NO₅
Molecular Weight:473.517
Hs Code.:

Synonyms:{4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

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Chemical Property of {4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

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Technology Process of {4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

There total 20 articles about {4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}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:

: 1402555-16-1
benzyl 4-[(1R,2S)-2-(2-{4-[2-(tert-butoxy)-2-oxoethyl]-2,5-difluorophenoxy}ethyl)cyclopropyl]piperidine-1-carboxylate

: 1402555-17-2
{4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 3.5h;

Reference yield:

: benzyl 4-{(1R,2S)-2-[2-(2-tert-butoxy-2-oxoethyl-2,5-difluorophenoxy)ethyl]cyclopropyl}piperidine-1-carboxylate

: 1402555-17-2
{4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 3.5h;

Reference yield:

: cis-tert-butyl 4-{2-[(2R)-3-(benzyloxy)-2-hydroxypropyl]cyclopropyl}piperidine-1-carboxylate

: 1402555-17-2
{4-[2-((1S,2R)-2-{1-[(benzyloxy)carbonyl]piperidin-4-yl}cyclopropyl)ethoxy]-2,5-difluorophenyl}acetic acid

Guidance literature:: Multi-step reaction with 8 steps

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

1.2: 0 °C

1.3: 0.5 h / 20 °C

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

3.1: triethylamine / dichloromethane / 20 °C

4.1: triethylamine / ethyl acetate / 4 h / Reflux

5.1: sodium hydrogencarbonate; dipotassium hydrogenphosphate / water; dimethyl sulfoxide; methanol / 7 h / 0 - 25 °C / pH 7 - 8

6.1: di-tert-butyl-diazodicarboxylate / dichloromethane / 4 h / 20 °C

7.1: XPhos / tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / diethyl ether; tetrahydrofuran / 65 °C / Inert atmosphere

8.1: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C

With hydrogenchloride; dipotassium hydrogenphosphate; di-tert-butyl-diazodicarboxylate; hydrogen; sodium hydrogencarbonate; triethylamine; trifluoroacetic acid; XPhos; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; palladium(II) hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; dichloromethane; water; dimethyl sulfoxide; ethyl acetate;