HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395610Generated: October 26, 2026
Imidazole → 2-(1-Imidazolyl)-4-dimethylamino-6-morpholino-1,3,5-triazine
https://huagongshe.com/reaction/2395610
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3,5-Triazin-2-amine, 4-chloro-N,N-dimethyl-6-(4-morpholinyl)- | HCID 10586342 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(1-Imidazolyl)-4-dimethylamino-6-morpholino-1,3,5-triazine | HCID 10564324 | 91.4% |
Reaction Steps
The obtained 2-chloro-4-dimethylamino-6-morpholino-1,3,5-triazine 492mg (2.02 mmol) was dissolved in DMF (20 ml), added with sodium hydroxide (182 mg, 4.55 mmol) and imidazole (308 mg, 4.52 mmol) and stirred at 110° C.-120° C. for 45 minutes. The reaction mixture was evaporated under reduced pressure. The residue obtained was added with dichloromethane and water, and then was shaken for mixing. The organic layer was separated from the mixture, washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography, using dichloromethane and methanol (95:5) as eluant, to obtain 508 mg (yield: 91.4%) of the titled compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05489591 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-ef8c3b85a43343ff9242c349ce1f5a3b |
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| Source note | uspto-grants-1996_02 |
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