(4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

Base Information

Chemical Name:(4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one
CAS No.:1374134-59-4
Molecular Formula:C₁₉H₁₆ClF₆N₃O₂S
Molecular Weight:499.864
Hs Code.:

Synonyms:(4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

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Chemical Property of (4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

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Technology Process of (4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

There total 7 articles about (4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-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:

: 875444-08-9
(4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one

: 1374134-65-2
5-chloro-4-methyl-2-(methylsulfanyl)-6-[(methylsulfonyl)methyl]pyrimidine

: 1374134-59-4
(4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

Guidance literature:: (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h;

5-chloro-4-methyl-2-(methylsulfanyl)-6-[(methylsulfonyl)methyl]pyrimidine; In tetrahydrofuran; at 0 - 20 ℃; for 4h;

Reference yield:

: 875444-08-9
(4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one

: C₈H₁₁ClN₂O₃S₂

: 1374134-59-4
(4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

Guidance literature:: (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h;

C₈H₁₁ClN₂O₃S₂; In tetrahydrofuran; at 0 - 20 ℃; for 4h;

Reference yield:

: 68087-13-8
6-[(methyloxy)methyl]-2-(methylthio)-4-pyrimidinol

: 1374134-59-4
(4S,5R)5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5-chloro-6-methyl-2-(methylsulfanyl)pyrimidin-4-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-chloro-succinimide / dichloromethane; N,N-dimethyl-formamide / 4 h / 20 °C

2.1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 - 20 °C

3.1: caesium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1 h / 140 °C

4.1: boron tribromide / dichloromethane / 1 h / 0 °C

5.1: triethylamine / dichloromethane / 0.5 h / 0 °C

6.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C

6.2: 4 h / 0 - 20 °C

With 2,6-dimethylpyridine; N-chloro-succinimide; boron tribromide; sodium hydride; caesium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;