HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635210Generated: October 30, 2026
2,4-Dichloro-6-methylpyrimidine → HCID 15512220, compound
https://huagongshe.com/reaction/635210
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichloro-6-methylpyrimidine | HCID 79471 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Phenyl-1,2,3,6-tetrahydropyridine hydrochloride | HCID 2723860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15512220 | HCID 15512220 | 67.5% |
Reaction Steps
In 4 ml of ethanol was dissolved 415 mg of 2,4-dichloro-6-methylpyrimidine, and the solution was cooled with ice-water. To the solution were added 503 mg of 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride and 664 mg of diisopropylethylamine, followed by stirring overnight under cooling with ice. The reaction solution was poured into a saturated aqueous solution of sodium hydrogencarbonate and extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The desiccant was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=10/1 to 3/1) to give 491 mg of 4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)-2-chloro-6-methylpyrimidine as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187781B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-b7143ff13d6141cfb09569a48565fd3a |
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| Source note | uspto-grants-2001_02 |
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