(2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine

Base Information

• Chemical Name: (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine
• CAS No.: 220630-47-7
• Molecular Formula: C₂₂H₁₉ClN₁₀
• Molecular Weight: 458.913
• Mol file: 220630-47-7.mol

Synonyms:(2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine

Chemical Property of (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine

There total 7 articles about (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine 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: 58.0%

2-azido-5-chlorobenzyl iodide (220630-35-3) + (2-Azidobenzyl)(2-azido-5-methylbenzyl)amine (220630-44-4) → (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine (220630-47-7)

Guidance literature:

In 1,4-dioxane; for 8h; Heating;

DOI:10.1002/(SICI)1521-3765(19981204)4:12<2558::AID-CHEM2558>3.0.CO;2-3

Reference yield:

2-amino-5-chlorobenzyl alcohol (37585-25-4) → (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine (220630-47-7)

Guidance literature:

Multi-step reaction with 4 steps

1: 1.) NaNO₂, H₂SO₄, H₂O, 2.) NaN₃ / 1.) 0 deg C, 30 min, 2.) 25 deg C, 16 h

2: 91 percent / SOCl₂ / CH₂Cl₂ / 3 h / 0 °C

3: 86 percent / NaI / acetone / 12 h / 25 °C

4: 58 percent / dioxane / 8 h / Heating

With thionyl chloride; sodium azide; sulfuric acid; water; sodium iodide; sodium nitrite; In 1,4-dioxane; dichloromethane; acetone;

DOI:10.1002/(SICI)1521-3765(19981204)4:12<2558::AID-CHEM2558>3.0.CO;2-3

Reference yield:

2-azido-5-methylbenzyl chloride (146954-08-7) → (2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine (220630-47-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 20 percent / NH₃ / 48 h / 25 °C

2: 39 percent / dioxane / 3 h / Heating

3: 58 percent / dioxane / 8 h / Heating

With ammonia; In 1,4-dioxane;

DOI:10.1002/(SICI)1521-3765(19981204)4:12<2558::AID-CHEM2558>3.0.CO;2-3

upstream raw materials:

2-azido-5-chlorobenzyl iodide

(2-Azidobenzyl)(2-azido-5-methylbenzyl)amine

2-amino-5-chlorobenzyl alcohol

1-azido-2-(bromomethyl)benzene

Downstream raw materials:

(2-Azidobenzyl)(2-azido-5-chlorobenzyl)(2-azido-5-methylbenzyl)amine N-oxide

N-{5-chloro-2-[N'-(4-methylphenyl)ureido]benzyl}-N-{5-methyl-2-[N'-(4-methylphenyl)ureido]benzyl}-N-{2-[N'-(4-methylphenyl)ureido]benzyl}amine

N-(2-aminobenzyl)-N-(2-amino-5-chlorobenzyl)-N-(2-amino-5-methylbenzyl)amine