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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621422Generated: November 2, 2026

Ethyl Acetate → 4-chloro-N-(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1621422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2,4-Dichloro-6-methyl-1,3,5-triazineHCID 16083—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantDiisopropylethylamineHCID 81531—
SolventDimethylformamideHCID 6228—
Product4-chloro-N-(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amineHCID 5954836095%

Reaction Steps

To a solution of 2,4-dichloro-6-methyl-1,3,5-triazine (190 g, 1159 mmol) in DMF (1500 mL) was added (4-methoxyphenyl)methanamine (159 g, 1159 mmol) slowly in 15 min while the temperature was controlled below 20° C. This was followed by the addition of N-ethyl-N-isopropylpropan-2-amine (222 mL, 1274 mmol) slowly over 15 min. After the completion of the reaction, EtOAc (2000 mL) was added and the mixture was washed with dilute brine (200 mL saturated NaCl plus 500 mL water), water (500 mL), saturated NH4Cl (250 mL), and finally water (250 mL). The organic layer was concentrated to afford 4-chloro-N-(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine as a solid (290.5 g, 1097 mmol, 95% yield). m/z 265.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-2dfca0d2ed3e47978f1ca3dd7affaa22
Source noteuspto-grants-2014_07