(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

Base Information

Chemical Name:(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one
CAS No.:1206791-16-3
Molecular Formula:C₂₈H₃₈N₂O₅S
Molecular Weight:514.686
Hs Code.:

Synonyms:(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

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Chemical Property of (S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

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Technology Process of (S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

There total 5 articles about (S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-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: 29.0%

: 1114573-35-1
(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-3-[(S)-1-(4-piperidin-4-yl-phenyl)-ethyl]-[1,3]oxazinan-2-one

: 124-63-0
methanesulfonyl chloride

: 1206791-16-3
(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 375853-82-0,286961-14-6
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-1(2H)-pyridinecarboxylate

: 1206791-16-3
(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

2: hydrogen / palladium 10% on activated carbon / methanol / 4 h / 2585.81 Torr

3: trifluoroacetic acid / dichloromethane / 20 °C

4: triethylamine / dichloromethane / 20 °C

With hydrogen; potassium carbonate; triethylamine; trifluoroacetic acid; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium 10% on activated carbon; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1110641-70-7
(S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one

: 1206791-16-3
(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methanesulfonyl-piperidin-4-yl)-phenyl]-ethyl}-6-phenyl-[1,3]oxazinan-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

2: hydrogen / palladium 10% on activated carbon / methanol / 4 h / 2585.81 Torr

3: trifluoroacetic acid / dichloromethane / 20 °C

4: triethylamine / dichloromethane / 20 °C

With hydrogen; potassium carbonate; triethylamine; trifluoroacetic acid; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium 10% on activated carbon; In methanol; dichloromethane; N,N-dimethyl-formamide;