(R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide

Base Information

• Chemical Name: (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide
• CAS No.: 178421-56-2
• Molecular Formula: C₂₁H₂₁N₃O₅
• Molecular Weight: 395.415
• Mol file: 178421-56-2.mol

Synonyms:(R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide

Chemical Property of (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide

There total 4 articles about (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-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:

phthalic anhydride (85-44-9) → (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide (178421-56-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 97 percent / triethylamine / toluene / 3 h / Heating

2: triethylamine / CH₂Cl₂ / 0.17 h / 0 °C

3: CH₂Cl₂ / 0.5 h / Ambient temperature

With triethylamine; In dichloromethane; toluene;

DOI:10.1016/0040-4020(96)00307-9

Reference yield:

(R)-4-nitro-phenylalanine (56613-61-7) → (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide (178421-56-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 97 percent / triethylamine / toluene / 3 h / Heating

2: triethylamine / CH₂Cl₂ / 0.17 h / 0 °C

3: CH₂Cl₂ / 0.5 h / Ambient temperature

With triethylamine; In dichloromethane; toluene;

DOI:10.1016/0040-4020(96)00307-9

Reference yield:

(R)-N-phthaloyl-p-nitrophenylalanine (131175-70-7,5467-31-2) → (R)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-nitro-phenyl)-propionamide (178421-56-2)

Guidance literature:

Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / 0.17 h / 0 °C

2: CH₂Cl₂ / 0.5 h / Ambient temperature

With triethylamine; In dichloromethane;

DOI:10.1016/0040-4020(96)00307-9

upstream raw materials:

tert-butylamine

phthalic anhydride

(R)-4-nitro-phenylalanine

(R)-N-phthaloyl-p-nitrophenylalanine

Downstream raw materials:

(2R,3S)-N-tert-Butyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-3-(4-nitro-phenyl)-propionamide

(2R,3S)-2-amino-3-hydroxy-3-(4-nitrophenyl)propionic acid