(R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
CAS No.:896746-83-1
Molecular Formula:C₂₄H₂₈N₂O₅
Molecular Weight:424.497
Hs Code.:

Synonyms:(R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

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Chemical Property of (R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

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Technology Process of (R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

There total 6 articles about (R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 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: 80.0%

: 660852-86-8,301155-28-2
(4R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-1,3-oxazolidine-4-carboxylic acid

: 2835-77-0
(2-aminophenyl)(phenyl)methanone

: 896746-83-1
(R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: (4R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-1,3-oxazolidine-4-carboxylic acid; With 4-methyl-morpholine; isobutyl chloroformate; In dichloromethane; at 0 - 20 ℃; for 0.5h;

(2-aminophenyl)(phenyl)methanone; In dichloromethane; Further stages.;
DOI:10.1021/jm701141u

Reference yield:

: 108149-60-6,95715-86-9
methyl [(4R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-1,3-oxazolidin-4-yl]carboxylate

: 896746-83-1
(R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: aq. LiOH / methanol / 6 h / 0 - 20 °C

2.1: N-methylmorpholine; isobutyl chloroformate / CH₂Cl₂ / 0.5 h / 0 °C

2.2: 5.07 g / CH₂Cl₂ / 13 h / 20 °C

With 4-methyl-morpholine; lithium hydroxide; isobutyl chloroformate; In methanol; dichloromethane;
DOI:10.1021/jm060405f

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 896746-83-1
(R)-4-(2-benzoyl-phenylcarbamoyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: aq. NaHCO₃ / tetrahydrofuran / 12 h / 20 °C

2.1: 4.56 g / BF₃*Et₂O / acetone / 2 h / 20 °C

3.1: aq. LiOH / methanol / 6 h / 0 - 20 °C

4.1: N-methylmorpholine; isobutyl chloroformate / CH₂Cl₂ / 0.5 h / 0 °C

4.2: 5.07 g / CH₂Cl₂ / 13 h / 20 °C

With 4-methyl-morpholine; lithium hydroxide; boron trifluoride diethyl etherate; sodium hydrogencarbonate; isobutyl chloroformate; In tetrahydrofuran; methanol; dichloromethane; acetone;
DOI:10.1021/jm060405f