L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide

Base Information

• Chemical Name: L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide
• CAS No.: 161219-94-9
• Molecular Formula: C₆₀H₆₀N₄O₉
• Molecular Weight: 981.158
• Mol file: 161219-94-9.mol

Synonyms:L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide

Chemical Property of L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide

There total 3 articles about L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide 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: 90.0%

2-hydroxybenzimino ethyl ether (20857-12-9) + L-N4-threonyl-N1,N8-bis-(2,3-dibenzyloxy-benzoyl)spermidine (161219-93-8) → L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide (161219-94-9)

Guidance literature:

In methanol; for 24h; Heating;

DOI:10.1016/S0040-4020(01)85669-6

Reference yield:

2,3-bis(benzyloxy)-N-(3-(4-(2,3-bis(benzyloxy)benzamido)butylamino)propyl)benzamide (74272-81-4) → L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide (161219-94-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 65 percent / dimethylformamide / 48 h / Ambient temperature

2: 56 percent / formic acid / 3 h / Ambient temperature

3: 90 percent / methanol / 24 h / Heating

With formic acid; In methanol; N,N-dimethyl-formamide;

DOI:10.1016/S0040-4020(01)85669-6

Reference yield:

L-N4--N1,N8-bis-(2,3-dibenzyloxybenzoyl)spermidine (161219-92-7) → L-N-<3-(2,3-dibenzyloxybenzamido)propyl>-N-<4-(2,3-dibenzyloxybenzamido)butyl>-2-(2-hydroxyphenyl)-trans-5-methyloxazoline-4-carboxamide (161219-94-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 56 percent / formic acid / 3 h / Ambient temperature

2: 90 percent / methanol / 24 h / Heating

With formic acid; In methanol;

DOI:10.1016/S0040-4020(01)85669-6

upstream raw materials:

2-hydroxybenzimino ethyl ether

L-N⁴-threonyl-N¹,N⁸-bis-(2,3-dibenzyloxy-benzoyl)spermidine

2,3-bis(benzyloxy)-N-(3-(4-(2,3-bis(benzyloxy)benzamido)butylamino)propyl)benzamide

L-N⁴--N¹,N⁸-bis-(2,3-dibenzyloxybenzoyl)spermidine

Downstream raw materials:

parabactin