(S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

Base Information

Chemical Name:(S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide
CAS No.:160648-63-5
Molecular Formula:C₂₁H₂₀N₂O₄
Molecular Weight:364.401
Hs Code.:

Synonyms:(S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

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Chemical Property of (S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

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Technology Process of (S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

There total 2 articles about (S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide 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: 67.0%

: 160648-48-6
(2S,3R)-3-hydroxy-N-t-butyl-N^α-phthaloylphenylalaninamide

: 160648-63-5
(S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

Guidance literature:: With jones reagent; In acetone; for 0.25h; Ambient temperature;
DOI:10.1016/S0040-4020(01)85256-X

Reference yield:

: 135395-16-3,135395-17-4,135501-57-4,135501-58-5
N-tert-Butyl-N^α-phthaloyl-β-bromophenylalaninamide

: 160648-63-5
(S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / AgNO₃ / acetone; H₂O / 24 h / Ambient temperature; in the dark

2: 67 percent / Jones reagent / acetone / 0.25 h / Ambient temperature

With jones reagent; silver nitrate; In water; acetone;
DOI:10.1016/S0040-4020(01)85256-X

Reference yield:

: 160648-63-5
(S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-3-phenyl-propionamide

: 6254-48-4
(2S,3R)-3-phenylserine

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄ / ethanol / 0.17 h / Ambient temperature

2: 78 percent / 6N aq. HCl / acetic acid / Heating

With hydrogenchloride; sodium tetrahydroborate; In ethanol; acetic acid;
DOI:10.1016/S0040-4020(01)85256-X