(3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester

Base Information

• Chemical Name: (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester
• CAS No.: 870640-36-1
• Molecular Formula: C₂₀H₃₁N₃O₅
• Molecular Weight: 393.483
• Mol file: 870640-36-1.mol

Synonyms:(3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester

Chemical Property of (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester

There total 4 articles about (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic 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: 78.0%

benzoic acid (65-85-0,8013-63-6) + di-tert-butyl (2-aminopropane-1,3-diyl)dicarbamate (149876-86-8) → (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester (870640-36-1)

Guidance literature:

With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 25 ℃;

DOI:10.1021/jm040208l

Reference yield:

(3-tert-butoxycarbonylamino-2-hydroxy-propyl)-carbamic acid tert-butyl ester (98642-15-0) → (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester (870640-36-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 84 percent / Et₃N / CH₂Cl₂ / 1 h / 20 °C

2: 94 percent / NaN₃ / dimethylformamide / 18 h / 100 °C

3: 82 percent / H₂ / Pd/C / methanol / 18 h / 2327.17 Torr

4: 78 percent / HOBt; DCC / tetrahydrofuran / 25 °C

With sodium azide; hydrogen; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm040208l

Reference yield:

methanesulfonic acid 2-tert-butoxycarbonylamino-1-(tert-butoxycarbonylaminomethyl)ethyl ester (129758-87-8) → (3-tert-butoxycarbonylamino-2-phenylacetylaminopropyl)carbamic acid tert-butyl ester (870640-36-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 94 percent / NaN₃ / dimethylformamide / 18 h / 100 °C

2: 82 percent / H₂ / Pd/C / methanol / 18 h / 2327.17 Torr

3: 78 percent / HOBt; DCC / tetrahydrofuran / 25 °C

With sodium azide; hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

DOI:10.1021/jm040208l

upstream raw materials:

benzoic acid

di-tert-butyl (2-aminopropane-1,3-diyl)dicarbamate

(3-tert-butoxycarbonylamino-2-hydroxy-propyl)-carbamic acid tert-butyl ester

methanesulfonic acid 2-tert-butoxycarbonylamino-1-(tert-butoxycarbonylaminomethyl)ethyl ester

Downstream raw materials:

N-{2-(2-cyanoacetylamino)-1-[1-(2-cyanoacetylamino)methyl]ethyl}benzamide

N-(2-amino-1-aminomethylethyl)benzamide