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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814903Generated: October 26, 2026

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

https://huagongshe.com/reaction/1814903

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 1/4, and 1/2). 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 numberUS06878717B2
Source datasetuspto-grants-2005_04
ORD IDord-3cad05aead234cd0bcc81bc1fbc5f162
Source noteuspto-grants-2005_04