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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435739Generated: October 30, 2026

4-Chloro-N-methylbenzenamine → HCID 9925034, compound

https://huagongshe.com/reaction/1435739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-N-methylbenzenamineHCID 70272—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 83240562HCID 83240562—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9925034HCID 992503422%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 4-chloro-6-(5-chloro-2-methyl-phenyl)-[1,3,5]triazin-2-yl-amine (106 mg, 0.42 mmol), (4-chloro-phenyl)-methyl-amine (0.15 ml, 1.25 mmol), tetrahydrofuran (5 ml), and diisopropylethylamine (0.75 ml, 4.2 mmol) was heated at 40° C. for 72 hours. The mixture was concentrated under reduced pressure and the residue was dissolved in dichloromethane (25 ml). The solution was washed with hydrochloric acid (1 M, 25 ml) and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with 2% methanol-dichloromethane followed by 5% methanol-dichloromethane. Recrystallization (ethyl acetate-hexane) provided the title compound (33 mg, 22% yield). 1H NMR (DMSO-d6) 7.78 (s, 1H), 7.37-7.46 (m, 4H), 7.26 (d, J=8.4 Hz, 1H), 7.10 (br s, 2H), 3.43 (s, 3H), 2.37 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618968B2
Source datasetuspto-grants-2009_11
ORD IDord-682b5e661728461c8974931673772162
Source noteuspto-grants-2009_11