Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062544Generated: November 2, 2026

Cyanuric chloride → 4-[[4-Chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrile

https://huagongshe.com/reaction/1062544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant4-AminobenzonitrileHCID 13396—
Reactant1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
ReactantMagnesiumHCID 5462224—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
SolventDiisopropylethylamineHCID 81531—
Product4-[[4-Chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrileHCID 486423104.2%

Reaction Steps

A solution of 2-(bromomethyl)-1,3-dichlorobenzene (about 10% of 0.383 mol) in diethylether (240 ml) was added to magnesium (0.383 mol) in diethylether (240 ml) under argon. Once the reaction started, the remainder of 2-(bromomethyl)-1,3-dichlorobenzene in diethylether was added. The solution was stirred at RT for 2.5 hours and then added via canula to a solution of 2,4,6-trichloro-1,3,5-triazine (0.319 mol) in benzene (480 ml) while keeping the temperature below 15° C. The reaction mixture was stirred for one hour in an ice bath, then for 2 hours at RT. A solution of 4-amino-benzonitrile (0.351 mol) in N,N-diisopropylethylamine (61.0 ml) and 1,4-dioxane (500 ml) was added and the reaction mixture was stirred at RT for 40 hours. The solvent was evaporated. Water and ethylacetate were added. The solution was stirred, then the solid was filtered off, washed with ethylacetate and water, yielding 129.9 g of 4-[[4-chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrile (intermediate 27; mp. 243-244° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962916B2
Source datasetuspto-grants-2005_11
ORD IDord-621d5965a54e4e849771a2f0b0ec59b9
Source noteuspto-grants-2005_11