HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796945Generated: October 25, 2026
2,4,6-Trimethylaniline → 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine
https://huagongshe.com/reaction/1796945
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trimethylaniline | HCID 6913 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromo-2,4-dichloropyrimidine | HCID 289973 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine | HCID 22170086 | 65% |
| Product | 5-bromo4-chloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamine | HCID 22170102 | 24% |
Reaction Steps
Reaction under argon atmosphere. A solution of 2,4,6-trimethylbenzenamine (0.00461 mol) in 1,4-dioxane (5 ml) was added to a solution of 5-bromo-2,4-dichloro-pyrimidine (0.00439 mol) in 1,4-dioxane (5 ml). N,N-bis(1-methylethyl)ethanamine (0.00548 mol) was added. The reaction mixture was stirred and refluxed for 20 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate, washed with a saturated aqueous sodium bicarbonate solution, water and brine, dried with sodium sulfate, filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: 1:5, 1:2 and 1:1 CH2Cl2: hexane). Two pure fraction groups were collected and their solvent was evaporated, yielding 0.35 g (24%) of 5-bromo-4-chloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamine (interm. 1) and 0.93 g (65%) of 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine (interm. 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034019B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-9a0e7025f382428e9013f6d75c4d12aa |
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| Source note | uspto-grants-2006_04 |
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