(2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

Base Information

Chemical Name:(2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde
CAS No.:121534-36-9
Molecular Formula:C₁₉H₁₄N₂O₄
Molecular Weight:334.331
Hs Code.:

Synonyms:(2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

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Chemical Property of (2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

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Technology Process of (2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

There total 6 articles about (2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde 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: 78.0%

: 121534-28-9
2-[(2S,3S)-1-Benzyl-2-((R)-3,3-dimethyl-oxiranyl)-4-oxo-azetidin-3-yl]-isoindole-1,3-dione

: 121534-36-9
(2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

Guidance literature:: With periodic acid; In diethyl ether; dichloromethane; at 25 ℃; for 12h;
DOI:10.1016/S0040-4039(00)80680-2

Reference yield: 78.0%

: 121534-29-0,121571-36-6,126575-09-5,126575-10-8
2-[(3S,4S)-1-Benzyl-2-oxo-4-((2R,3S)-3-phenyl-oxiranyl)-azetidin-3-yl]-isoindole-1,3-dione

: 121534-36-9
(2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

Guidance literature:: With periodic acid; In diethyl ether; dichloromethane; at 25 ℃; for 12h;
DOI:10.1016/S0040-4039(00)80680-2

Reference yield:

: 6780-38-7
N-phthaloylglycine chloride

: 121534-36-9
(2S,3S)-1-Benzyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-oxo-azetidine-2-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / triethylamine / CH₂Cl₂ / addition of triethylamine at -78 deg C, 0 deg C 3-5 h

2: 78 percent / periodic acid / diethyl ether; CH₂Cl₂ / 12 h / 25 °C

With periodic acid; triethylamine; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4039(00)80680-2