4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

Base Information

Chemical Name:4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester
CAS No.:512784-00-8
Molecular Formula:C₃₇H₃₈F₃N₃O₆
Molecular Weight:677.72
Hs Code.:

4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid <i>tert</i>-butyl ester

Synonyms:4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

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Chemical Property of 4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

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Technology Process of 4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

There total 7 articles about 4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric 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:

: 512783-86-7
N-[(benzyloxy)carbonyl]-D-glutamic acid γ-tert-butyl ester α-[3-(trifluoromethyl)benzyl]amide

: 512784-00-8
4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / hydrogen / palladium on carbon / methanol

2: magnesium sulfate / CH₂Cl₂ / 20 °C

3: 1.84 mg / amine / CH₂Cl₂ / 1 h / 0 - 20 °C

With hydrogen; magnesium sulfate; palladium on activated charcoal; In methanol; dichloromethane; 3: Staudinger cycloaddition;
DOI:10.1016/j.bmc.2006.12.031

Reference yield:

: 2740-83-2
3-(TRIFLUOROMETHYL)BENZYLAMINE

: 512784-00-8
4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide*HCl; HOAt / CH₂Cl₂ / 20 °C

2: 94 percent / hydrogen / palladium on carbon / methanol

3: magnesium sulfate / CH₂Cl₂ / 20 °C

4: 1.84 mg / amine / CH₂Cl₂ / 1 h / 0 - 20 °C

With 1-hydroxy-7-aza-benzotriazole; hydrogen; magnesium sulfate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In methanol; dichloromethane; 4: Staudinger cycloaddition;
DOI:10.1016/j.bmc.2006.12.031

Reference yield:

: 51644-83-8
N-(benzyloxy)carbonyl-D-glutamic acid 5-tert-butyl ester

: 512784-00-8
4-[2-oxo-3-(2-oxo-4-phenyl-oxazolidin-3-yl)-4-styryl-azetidin-1-yl]-4-(3-trifluoromethyl-benzylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide*HCl; HOAt / CH₂Cl₂ / 20 °C

2: 94 percent / hydrogen / palladium on carbon / methanol

3: magnesium sulfate / CH₂Cl₂ / 20 °C

4: 1.84 mg / amine / CH₂Cl₂ / 1 h / 0 - 20 °C

With 1-hydroxy-7-aza-benzotriazole; hydrogen; magnesium sulfate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In methanol; dichloromethane; 4: Staudinger cycloaddition;
DOI:10.1016/j.bmc.2006.12.031