(RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one

Base Information

• Chemical Name: (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one
• CAS No.: 221526-71-2
• Molecular Formula: C₂₃H₂₈N₂O₇S₂
• Molecular Weight: 508.617
• Mol file: 221526-71-2.mol

Synonyms:(RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one

Chemical Property of (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one

There total 6 articles about (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-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: 73.0%

1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one (7744-25-4) + (S)-3-Benzenesulfonyl-2,2-dimethyl-oxazolidine-4-carboxylic acid (637773-08-1) → (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one (221526-71-2)

Guidance literature:

With lithium hexamethyldisilazane; In tetrahydrofuran; at -60 ℃; for 11h;

DOI:10.1016/S0040-4039(98)80033-6

Reference yield: 72.0%

1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one (7744-25-4) + (4S)-3-benzenesulfonyl-4-formyl-2,2-dimethyl-3-oxazolidine (221526-69-8) → (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one (221526-71-2)

Guidance literature:

With lithium hexamethyldisilazane; In tetrahydrofuran; at -60 ℃; for 12h;

Reference yield:

methyl N-benzenesulfonyl-L-serinate (221526-66-5) → (RS)-1-benzenesulfonyl-3-[(RS)-[(4S)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]hydroxymethyl]piperidin-2-one (221526-71-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 90 percent / p-TsOH*H₂O / benzene / 2 h / Heating

2: 92 percent / DIBAH / toluene / 3 h / -78 - 20 °C

3: 72 percent / LiN(TMS)2 / tetrahydrofuran / 12 h / -60 °C

With diisobutylaluminium hydride; toluene-4-sulfonic acid; lithium hexamethyldisilazane; In tetrahydrofuran; toluene; benzene;

upstream raw materials:

1-Benzenesulfonyl-3,4,5,6-tetrahydropyridin-2-one

(S)-3-Benzenesulfonyl-2,2-dimethyl-oxazolidine-4-carboxylic acid

(4S)-3-benzenesulfonyl-4-formyl-2,2-dimethyl-3-oxazolidine

piperidin-2-one

Downstream raw materials:

(RS)-1-benzenesulfonyl-3-[(4R)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-ylmethyl]-piperidin-2-one

1-benzenesulfonyl-3-[(4R)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-ylmethyl]-5,6-dihydro-1H-pyridin-2-one

(RS)-1-benzenesulfonyl-3-[(4R)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-ylmethyl]-3-phenylthiopiperidin-2-one

(4aR,8aR)-2-benzenesulfonyl-8a-[(4R)-3-benzenesulfonyl-2,2-dimethyloxazolidin-4-yl]methyl-1,2,3,4,4a,5,6,8a-octahydroisoquinoline-1,6-dione