2-Oxa-4,8,13-triazatetradecan-14-oic acid, 3-oxo-1-phenyl-, phenylmethyl ester

Base Information

• Chemical Name: 2-Oxa-4,8,13-triazatetradecan-14-oic acid, 3-oxo-1-phenyl-, phenylmethyl ester
• CAS No.: 89965-56-0
• Molecular Formula: C23H31N3O4
• Molecular Weight: 413.51000

Synonyms:benzyl{4-[(3-{[(benzyloxy)carbonyl]amino}propyl)amino]butyl}carbamate;benzyl N-((8-(benzyloxycarbonyl)amino)-4-azaoctyl)carbamate;N1,N8-bis-(phenylmethoxycarbonyl)spermidine;N1,N10-di[(benzyloxy)carbonyl]spermidine;N1,N10-bis(benzyloxycarbonyl)spermidine;benzyl N-(8-{[(benzyloxy)carbonyl]amino}-4-azaoctyl)carbamate;

Chemical Property of 2-Oxa-4,8,13-triazatetradecan-14-oic acid, 3-oxo-1-phenyl-, phenylmethyl ester

Chemical Property:

• Boiling Point: 606.9±55.0 °C(Predicted)
• PSA: 88.69000
• Density: 1.133±0.06 g/cm3(Predicted)
• LogP: 4.77180

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

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Technology Process of 2-Oxa-4,8,13-triazatetradecan-14-oic acid, 3-oxo-1-phenyl-, phenylmethyl ester

There total 10 articles about 2-Oxa-4,8,13-triazatetradecan-14-oic acid, 3-oxo-1-phenyl-, phenylmethyl 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: 99.0%

N-(3-aminopropyl)-1,4-diaminobutane (124-20-9) + benzyl cyanoformate (5532-86-5) → <3-<<4-(carboxyamino)butyl>amino>propyl>carbamic acid, dibenzyl ester (89965-56-0)

Guidance literature:

In dichloromethane; at 20 ℃; for 3h;

DOI:10.1246/cl.1987.879

Reference yield: 76.0%

N-benzyloxycarbonylimidazole (22129-07-3) + N-(3-aminopropyl)-1,4-diaminobutane (124-20-9) → <3-<<4-(carboxyamino)butyl>amino>propyl>carbamic acid, dibenzyl ester (89965-56-0)

Guidance literature:

With dmap; In dichloromethane; for 16h; Ambient temperature;

DOI:10.1021/jm00122a013

Reference yield: 71.0%

N-(3-aminopropyl)-1,4-diaminobutane (124-20-9) + benzyl phenyl carbonate (28170-07-2) → <3-<<4-(carboxyamino)butyl>amino>propyl>carbamic acid, dibenzyl ester (89965-56-0)

Guidance literature:

In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1055/s-2002-34859

upstream raw materials:

N-benzyloxycarbonylimidazole

N-(3-aminopropyl)-1,4-diaminobutane

benzyl cyanoformate

3-benzyloxycarbonyl-1,3-thiazolidine-2-thione

Downstream raw materials:

(4S,5R)-N-<3-(benzyloxycarbonylamino)propyl>-N-<4-(benzyloxycarbonylamino)butyl>-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-oxazole-4-carboxamide

N⁴-(N-Methyl-N-(benzyloxy)succinamoyl)-N¹,N⁸-dicarbobenzoxyspermidine

N⁴-((p-Nitrobenzyl)succinoyl)-N¹,N⁸-dicarbobenzoxyspermidine

N⁴-(Benzylsuccinoyl)-N¹,N⁸-dicarbobenzoxyspermidine

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