(R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

Base Information

Chemical Name:(R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate
CAS No.:1353255-06-7
Molecular Formula:C₁₉H₂₆F₂N₂O₄
Molecular Weight:384.423
Hs Code.:

Synonyms:(R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

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Chemical Property of (R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

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Technology Process of (R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

There total 3 articles about (R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate 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:

: 309956-78-3,172603-05-3
(R)-piperidin-3-ylcarbamic acid tert-butyl ester

: 1353255-02-3
methyl bromo(2,6-difluorophenyl)acetate

: 1353255-06-7
(R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

: 1353255-04-5
(S)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 90 ℃; for 18h; Microwave irradiation;

Reference yield:

: 85068-28-6
2,6-difluorophenylacetic acid

: 1353255-06-7
(R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

: 1353255-04-5
(S)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / diethyl ether; tetrahydrofuran / 2 h / 20 °C

2: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / 42 h / Reflux

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 90 °C / Microwave irradiation

With methanol; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; tetrachloromethane; diethyl ether; acetonitrile;

Reference yield:

: 872046-08-7
(2,6-difluorophenyl)acetic acid methyl ester

: 1353255-06-7
(R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

: 1353255-04-5
(S)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / 42 h / Reflux

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 90 °C / Microwave irradiation

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); N-ethyl-N,N-diisopropylamine; In tetrachloromethane; acetonitrile;