(3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate

Base Information

• Chemical Name: (3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate
• CAS No.: 215999-75-0
• Molecular Formula: C₃₄H₄₄N₄O₆
• Molecular Weight: 604.747
• Mol file: 215999-75-0.mol

Synonyms:(3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate

Chemical Property of (3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate

There total 1 articles about (3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate 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: 85.0%

Spermine (71-44-3) + benzyl cyanoformate (5532-86-5) → (3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate (215999-75-0)

Guidance literature:

With triethylamine; In chloroform;

DOI:10.1002/hlca.19960790221

Reference yield: 98.0%

(3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate (215999-75-0) + 2-(benzyloxy)benzene-1,3,5-tris[propionic acid] (322638-61-9) → 2-(benzyloxy)-N,N',N-tris(3-{[(benzyloxy)carbonyl]amino}propyl)-N,N',N-tris(4-{[(benzyloxy)carbonyl](3-{[(benzyloxy)carbonyl]amino}propyl)amino}butyl)benzene-1,3,5-tris[propanamide]

Guidance literature:

With 2-chloro-1-methyl-pyridinium iodide; triethylamine; In dichloromethane; at 20 ℃;

DOI:10.1002/1522-2675(20001108)83:11<3021::AID-HLCA3021>3.0.CO;2-E

Reference yield: 95.0%

(3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate (215999-75-0) + 2-(benzyloxy)-5-(tert-butyl)benzene-1,3-bis[propionic acid] (322638-50-6) → 2-(benzyloxy)-N,N'-bis(4-{[(benzyloxy)carbonyl](3-{[(benzyloxy)carbonyl]amino}propyl)amino}butyl)-N,N'-bis(3-{[(benzyloxy)carbonyl]amino}propyl)-5-(tert-butyl)benzene-1,3-bis[propanamide]

Guidance literature:

2-(benzyloxy)-5-(tert-butyl)benzene-1,3-bis[propionic acid]; With 2-chloro-1-methyl-pyridinium iodide; triethylamine; In dichloromethane; at 20 ℃; for 0.5h;

(3-{[(benzyloxy)carbonyl]amino}propyl){4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate; In dichloromethane; at 20 ℃;

DOI:10.1002/1522-2675(20001108)83:11<3021::AID-HLCA3021>3.0.CO;2-E

upstream raw materials:

Spermine

benzyl cyanoformate