tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate
CAS No.:1365998-55-5
Molecular Formula:C₂₁H₂₈F₂N₂O₆S
Molecular Weight:474.526
Hs Code.:

Synonyms:tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

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Chemical Property of tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

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Technology Process of tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

There total 4 articles about tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate 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: 48.0%

: 1365998-54-4
tert-butyl 4-(3-(4-bromo-2,5-difluorophenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

: 20277-69-4
sodium methansulfinate

: 1365998-55-5
tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

Guidance literature:: copper(I) trifluoromethanesulfonate benzene; trans-1,2-cyclohexanediamine; In dimethyl sulfoxide; at 110 ℃; Product distribution / selectivity; Inert atmosphere;

Reference yield:

: 87120-72-7
1-(tert-butoxycarbonyl)-4-aminopiperidine

: 1365998-55-5
tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 0 °C

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 - 20 °C

3: potassium carbonate / acetone / 20 °C

4: trans-1,2-cyclohexanediamine; copper(I) trifluoromethanesulfonate benzene / dimethyl sulfoxide / 110 °C / Inert atmosphere

With sodium hydride; potassium carbonate; triethylamine; copper(I) trifluoromethanesulfonate benzene; trans-1,2-cyclohexanediamine; In dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone; mineral oil;

Reference yield:

: 1351168-97-2
tert-butyl 4-(3-bromo-2-oxo-pyrrolidin-1-yl)piperidine-1-carboxylate

: 1365998-55-5
tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetone / 20 °C

2: trans-1,2-cyclohexanediamine; copper(I) trifluoromethanesulfonate benzene / dimethyl sulfoxide / 110 °C / Inert atmosphere

With potassium carbonate; copper(I) trifluoromethanesulfonate benzene; trans-1,2-cyclohexanediamine; In dimethyl sulfoxide; acetone;