N-(4-tert-Butylphenyl)-4,6-dichloro-1,3,5-triazin-2-amine

Base Information

• Chemical Name: N-(4-tert-Butylphenyl)-4,6-dichloro-1,3,5-triazin-2-amine
• CAS No.: 146887-20-9
• Molecular Formula: C13H14Cl2N4
• Molecular Weight: 297.187
• DSSTox Substance ID: DTXSID40598678
• Wikidata: Q82494460
• Mol file: 146887-20-9.mol

Synonyms:146887-20-9;N-(4-tert-Butylphenyl)-4,6-dichloro-1,3,5-triazin-2-amine;SCHEMBL5471034;DTXSID40598678;IBQFPEHHCPPHHY-UHFFFAOYSA-N;AKOS009154541;(4-tert-butyl-phenyl)-(4,6-dichloro-[1,3,5]triazin-2-yl)-amine

Chemical Property of N-(4-tert-Butylphenyl)-4,6-dichloro-1,3,5-triazin-2-amine

Chemical Property:

• XLogP3: 5.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 296.0595519
• Heavy Atom Count: 19
• Complexity: 277

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)C1=CC=C(C=C1)NC2=NC(=NC(=N2)Cl)Cl

Technology Process of N-(4-tert-Butylphenyl)-4,6-dichloro-1,3,5-triazin-2-amine

There total 2 articles about N-(4-tert-Butylphenyl)-4,6-dichloro-1,3,5-triazin-2-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: 83.0%

1,3,5-trichloro-2,4,6-triazine (108-77-0) + 4-tert-Butylaniline (769-92-6) → (4-tert-butylphenyl)-(4,6-dichloro-[1,3,5]triazin-2-yl)-amine (146887-20-9)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 - 20 ℃; for 3h; Inert atmosphere;

DOI:10.1021/acs.jmedchem.1c01551

Reference yield:

→ (4-tert-butylphenyl)-(4,6-dichloro-[1,3,5]triazin-2-yl)-amine (146887-20-9)

Guidance literature:

Reference yield: 70.0%

tert-butyl {2-[2-(2-aminoethoxy)ethoxy]ethyl}carbamate (153086-78-3) + (4-tert-butylphenyl)-(4,6-dichloro-[1,3,5]triazin-2-yl)-amine (146887-20-9) → tert-butyl (2-(2-(2-((4-((4-(tert-butyl)phenyl)amino)-6-chloro-1,3,5-triazin-2-yl)amino)ethoxy)ethoxy)ethyl)carbamate

Guidance literature:

With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; for 3h; Inert atmosphere;

DOI:10.1021/acs.jmedchem.1c01551

upstream raw materials:

1,3,5-trichloro-2,4,6-triazine

4-tert-Butylaniline

Downstream raw materials:

(5-{[4-(4-tert-Butyl-phenylamino)-6-chloro-[1,3,5]triazin-2-ylamino]-methyl}-2,4-diisopropyl-benzyl)-carbamic acid tert-butyl ester

1,3-N,N'-bis[4-chloro-6-(tert-butylamino)-1,3,5-triazin-2-yl]xylene diamine

4-chloro-2-(4'-tert-butylanilino)-6-dibutylamino-1,3,5-triazine

2-chloro-4-(4-tertbutylphenylamino)-6-(4-iodophenylamino)-1,3,5-triazine

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