3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

Base Information

Chemical Name:3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one
CAS No.:1365998-56-6
Molecular Formula:C₁₆H₂₀F₂N₂O₄S
Molecular Weight:374.409
Hs Code.:

Synonyms:3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

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Chemical Property of 3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

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Technology Process of 3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

There total 5 articles about 3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one 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%

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

: 1365998-56-6
3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

Guidance literature:: tert-butyl 4-(3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate; With hydrogenchloride; In ethyl acetate; isopropyl alcohol; at 0 - 20 ℃;

With sodium hydroxide; In ethyl acetate; isopropyl alcohol; Product distribution / selectivity;

Reference yield:

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

: 1365998-56-6
3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 5 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

5: hydrogenchloride / ethyl acetate; isopropyl alcohol / 0 - 20 °C

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

Reference yield:

: 1365998-53-3
tert-butyl 4-(2,4-dibromobutanamido)piperidin-1-carboxylate

: 1365998-56-6
3-(2,5-difluoro-4-(methylsulfonyl)phenoxy)-1-(piperidin-4-yl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

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

2: potassium carbonate / acetone / 20 °C

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

4: hydrogenchloride / ethyl acetate; isopropyl alcohol / 0 - 20 °C

With hydrogenchloride; sodium hydride; potassium carbonate; copper(I) trifluoromethanesulfonate benzene; trans-1,2-cyclohexanediamine; In dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; acetone; mineral oil;