N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide

Base Information

• Chemical Name: N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide
• CAS No.: 126111-90-8
• Molecular Formula: C₂₈H₃₈Cl₂N₂O₅
• Molecular Weight: 553.526
• Mol file: 126111-90-8.mol

Synonyms:N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide

Chemical Property of N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide

There total 3 articles about N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide 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: 82.0%

1,15-Diphenyl-6,9,12-trioxa-2,16-diazaheptadecane (126111-87-3) + chloroacetyl chloride (79-04-9) → N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide (126111-90-8)

Guidance literature:

With potassium carbonate; In chloroform; water; for 2h; Ambient temperature;

DOI:10.1021/jo00297a068

Reference yield:

4,7,10-trioxa-1,13-diaminotridecane (4246-51-9) → N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide (126111-90-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 2) NaBH₄ / methanol, 1) 0 - 5 deg C, 15 min; 2) 0 - 5 deg C, 2 h

2: 82 percent / K₂CO₃ / CHCl₃; H₂O / 2 h / Ambient temperature

With sodium tetrahydroborate; potassium carbonate; In chloroform; water;

DOI:10.1021/jo00297a068

Reference yield:

benzaldehyde (100-52-7) → N-Benzyl-N-{3-[2-(2-{3-[benzyl-(2-chloro-acetyl)-amino]-propoxy}-ethoxy)-ethoxy]-propyl}-2-chloro-acetamide (126111-90-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 2) NaBH₄ / methanol, 1) 0 - 5 deg C, 15 min; 2) 0 - 5 deg C, 2 h

2: 82 percent / K₂CO₃ / CHCl₃; H₂O / 2 h / Ambient temperature

With sodium tetrahydroborate; potassium carbonate; In chloroform; water;

DOI:10.1021/jo00297a068

upstream raw materials:

1,15-Diphenyl-6,9,12-trioxa-2,16-diazaheptadecane

chloroacetyl chloride

4,7,10-trioxa-1,13-diaminotridecane

benzaldehyde

Downstream raw materials:

[2-(11,17-Dibenzyl-1,4,7-trioxa-11,14,17-triaza-cycloicos-14-yl)-ethyl]-ethyl-amine