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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41365Generated: October 24, 2026

2,4,6-Trimethylaniline → 2,5,6-trichloro-N-(2,4,6-trimethylphenyl)4-pyrimidinamine

https://huagongshe.com/en/reaction/41365

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylanilineHCID 6913—
Reactant2,4,5,6-TetrachloropyrimidineHCID 15690—
ReactantDiisopropylethylamineHCID 81531—
Solvent1,4-DioxaneHCID 31275—
Product2,5,6-trichloro-N-(2,4,6-trimethylphenyl)4-pyrimidinamineHCID 22170091—
Product4,5,6-trichloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamineHCID 22170094—

Reaction Conditions

Temperature55 °C

Reaction Steps

2,4,5,6-tetrachloropyrimidine (0.0134 mol), 1,4-dioxane (30 ml), 2,4,6-trimethyl aniline (0.0134 mol), and N,N-bis(1-methylethyl)ethanamine (0.0136 mol) were added to a flask under argon and stirred at 55° C. for 16 hours. The solvent was evaporated, and the residue was dissolved in CH2Cl2, then purified by column chromatography over silica gel (eluent: CH2Cl2/hexane ¼, and ½). The desired fractions were collected and their solvent was evaporated, yielding 0.15 g 4,5,6-trichloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamine (interm. 6) and 3.15 g 2,5,6-trichloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine (interm. 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530655B2
Source datasetuspto-grants-2013_09
ORD IDord-489dd9ecf56a4150bd590657d4a5ef5d
Source noteuspto-grants-2013_09