(2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester

Base Information

• Chemical Name: (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester
• CAS No.: 940055-55-0
• Molecular Formula: C₂₇H₂₄FN₃O₆
• Molecular Weight: 505.502
• Mol file: 940055-55-0.mol

Synonyms:(2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester

Chemical Property of (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester

There total 5 articles about (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl 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:

N-(Benzyloxycarbonyloxy)succinimide (13139-17-8) + 3-(2-amino-4-fluorobenzylamino)-pyrrolidine-2,5-dione (940054-58-0) → (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester (940055-55-0)

Guidance literature:

dmap; In tetrahydrofuran; at 20 ℃; for 24h;

Reference yield:

4-fluoroanthranilamide (119023-25-5) → (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester (940055-55-0)

Guidance literature:

Multi-step reaction with 3 steps

1: dimethylsulfide borane complex / tetrahydrofuran / 9 h / Heating / reflux

2: ethyl acetate / 41 h / 20 - 50 °C

3: dmap / tetrahydrofuran / 24 h / 20 °C

With dimethylsulfide borane complex; dmap; In tetrahydrofuran; ethyl acetate;

Reference yield:

4-fluoroanthranilic acid (446-32-2) → (2-{[benzyloxycarbonyl-(2,5-dioxopyrrolidin-3-yl)-amino]-methyl}-5-fluorophenyl)-carbamic acid benzyl ester (940055-55-0)

Guidance literature:

Multi-step reaction with 5 steps

1: triethylamine / acetone / 48 h / 20 °C

2: ammonia / 1,4-dioxane; water / 20 h / 100 °C

3: dimethylsulfide borane complex / tetrahydrofuran / 9 h / Heating / reflux

4: ethyl acetate / 41 h / 20 - 50 °C

5: dmap / tetrahydrofuran / 24 h / 20 °C

With dimethylsulfide borane complex; ammonia; triethylamine; dmap; In tetrahydrofuran; 1,4-dioxane; water; ethyl acetate; acetone;

upstream raw materials:

N-(Benzyloxycarbonyloxy)succinimide

3-(2-amino-4-fluorobenzylamino)-pyrrolidine-2,5-dione

2-aminomethyl-5-fluoro-aniline

2-amino-4-fluorobenzoic acid cyanomethyl ester

Downstream raw materials:

(2-{[benzyloxycarbonyl-(2-oxo-5-thioxopyrrolidin-3-yl)amino]methyl}-5-fluorophenyl)-carbamoyl acid benzyl ester