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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trimethylaniline | HCID 6913 | — |
| Reactant | 2,4,5,6-Tetrachloropyrimidine | HCID 15690 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,5,6-trichloro-N-(2,4,6-trimethylphenyl)4-pyrimidinamine | HCID 22170091 | — |
| Product | 4,5,6-trichloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamine | HCID 22170094 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530655B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-489dd9ecf56a4150bd590657d4a5ef5d |
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| Source note | uspto-grants-2013_09 |
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