3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

Base Information

Chemical Name:3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one
CAS No.:300592-66-9
Molecular Formula:C₂₅H₂₅NO₃S
Molecular Weight:419.544
Hs Code.:

Synonyms:3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

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Chemical Property of 3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

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Technology Process of 3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

There total 1 articles about 3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-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: 81.0%

: 529-36-2
1-Naphthalenethiol

: 113543-35-4
(4S)-3-((2S)-2-bromo-3-methylbutanoyl)-4-benzyl-1,3-oxazolidin-2-one

: 300592-66-9
3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1021/ja992543i

Reference yield:

: 300592-66-9
3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

: [(2R,3R)-3-(1-naphthylthio)-4-methylpent-2-oxy]diphenylphosphine

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / LiBH₄ / tetrahydrofuran; H₂O / 3 h / 0 °C

2.1: oxalyl chloride; DMSO; DIPEA / CH₂Cl₂ / -78 - -50 °C

3.1: 15 percent / diethyl ether; CH₂Cl₂ / 0.5 h / -78 °C

4.1: n-BuLi / tetrahydrofuran; hexane / 1 h / 20 °C

4.2: 8 percent / tetrahydrofuran; hexane / 3 h / 20 °C

With lithium borohydride; n-butyllithium; oxalyl dichloride; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; 2.1: Swern oxidation;
DOI:10.1021/ja992543i

Reference yield:

: 300592-66-9
3-[(2R)-2-(1-naphthylthio)-3-methylbutanoyl]-(4S)-4-benzyl-1,3-oxazolidin-2-one

: [(2S,3R)-3-(1-naphthylthio)-4-methylpent-2-oxy]diphenylphosphine

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / LiBH₄ / tetrahydrofuran; H₂O / 3 h / 0 °C

2.1: oxalyl chloride; DMSO; DIPEA / CH₂Cl₂ / -78 - -50 °C

3.1: 60 percent / diethyl ether; CH₂Cl₂ / 0.5 h / -78 °C

4.1: n-BuLi / tetrahydrofuran; hexane / 1 h / 20 °C

4.2: 44 percent / tetrahydrofuran; hexane / 3 h / 20 °C

With lithium borohydride; n-butyllithium; oxalyl dichloride; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; 2.1: Swern oxidation;
DOI:10.1021/ja992543i