(3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

Base Information

Chemical Name:(3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one
CAS No.:867171-65-1
Molecular Formula:C₂₄H₃₆N₂O₄
Molecular Weight:416.561
Hs Code.:

Synonyms:(3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

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Chemical Property of (3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

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Technology Process of (3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

There total 3 articles about (3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-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: 76.0%

: 867171-59-3
(3R,4S)-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-isopropyl-3-methylazetidin-2-one

: 100-39-0
benzyl bromide

: 867171-65-1
(3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

Guidance literature:: With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; water; at 20 ℃; for 2h;
DOI:10.1016/j.tetasy.2005.07.023

Reference yield:

: 867171-51-5
(3S,4R)-2-benzyl-3-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-4-isopropyl-4-methylisoxazolidin-5-one

: 867171-65-1
(3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen / Pd/C / methanol / 2 h / 20 °C / 3040 Torr

2: 58 percent / MsCl; Bu₄NHSO₄; KHCO₃ / H₂O; CHCl₃ / 0.5 h / 20 °C

3: 76 percent / sodium hydroxide; Bu₄NHSO₄ / H₂O; CH₂Cl₂ / 2 h / 20 °C

With sodium hydroxide; hydrogen; tetra(n-butyl)ammonium hydrogensulfate; potassium hydrogencarbonate; methanesulfonyl chloride; palladium on activated charcoal; In methanol; dichloromethane; chloroform; water;
DOI:10.1016/j.tetasy.2005.07.023

Reference yield:

: 867171-76-4
(R)-4-((1S,2R)-1-Amino-2-carboxy-2,3-dimethyl-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 867171-65-1
(3R,4S)-1-benzyl-4-((R)-3-tert-butoxycarbonyl-2,2-dimethyloxazolidin-4-yl)-3-butyl-3-isopropylazetidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / MsCl; Bu₄NHSO₄; KHCO₃ / H₂O; CHCl₃ / 0.5 h / 20 °C

2: 76 percent / sodium hydroxide; Bu₄NHSO₄ / H₂O; CH₂Cl₂ / 2 h / 20 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; potassium hydrogencarbonate; methanesulfonyl chloride; In dichloromethane; chloroform; water;
DOI:10.1016/j.tetasy.2005.07.023