(4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

Base Information

Chemical Name:(4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one
CAS No.:868669-87-8
Molecular Formula:C₂₆H₃₁F₂N₃O₄S
Molecular Weight:519.613
Hs Code.:

Synonyms:(4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

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Chemical Property of (4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

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Technology Process of (4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

There total 4 articles about (4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-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:

: 833491-23-9
(4R,5S)-1,5-dimethyl-3-{(2E)-3-[1-(methylsulfonyl)piperidin-4-yl]prop-2-enoyl}-4-phenylimidazolidin-2-one

: 868669-87-8
(4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

Guidance literature:: 3,5-difluorophenylmagnesium bromide; With copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; In tetrahydrofuran; at -70 ℃; for 0.666667h;

(4R,5S)-1,5-dimethyl-3-{(2E)-3-[1-(methylsulfonyl)piperidin-4-yl]prop-2-enoyl}-4-phenylimidazolidin-2-one; With di-n-butylboron trifluoromethanesulphonate; In tetrahydrofuran; dichloromethane; at -70 - 20 ℃; for 1h;

With water; ammonium chloride; In tetrahydrofuran; dichloromethane;

Reference yield:

: 833491-23-9
(4R,5S)-1,5-dimethyl-3-{(2E)-3-[1-(methylsulfonyl)piperidin-4-yl]prop-2-enoyl}-4-phenylimidazolidin-2-one

: 62351-47-7
3,5-difluorophenylmagnesium bromide

: 868669-87-8
(4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

Guidance literature:: 3,5-difluorophenylmagnesium bromide; With copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; In tetrahydrofuran; at -70 ℃; for 1.41667h;

(4R,5S)-1,5-dimethyl-3-{(2E)-3-[1-(methylsulfonyl)piperidin-4-yl]prop-2-enoyl}-4-phenylimidazolidin-2-one; With di-n-butylboryl trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane; at -70 - 20 ℃; for 1.16667h;

With water; ammonium chloride; In tetrahydrofuran; dichloromethane; at 20 ℃;

Reference yield:

: 833491-33-1
3-(N-methanesulphonylpiperidin-4-yl)propenoic acid

: 868669-87-8
(4S,5R)-1-{(3R)-3-(3,5-difluorophenyl)-3-[1-(methylsulfonyl)piperidin-4-yl]propanoyl}-3,4-dimethyl-5-phenylimidazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / dichloromethane / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / 20 °C

3.1: copper(l) iodide; N,N,N,N,-tetramethylethylenediamine / tetrahydrofuran / -78 °C

3.2: -78 - 20 °C

With copper(l) iodide; thionyl chloride; N,N,N,N,-tetramethylethylenediamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2011.12.117