HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14573Generated: October 25, 2026
Potassium Carbonate → 1-(6-chloro-5-fluoropyrimidin-4-yl)-trans-2,6-dimethylhexahydro-1H-azepine
https://huagongshe.com/reaction/14573
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4,6-Dichloro-5-fluoropyrimidine | HCID 11286675 | — |
| Reactant | trans-2,6-dimethylhexahydro-1H-azepine hydrochloride | HCID 66594500 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(6-chloro-5-fluoropyrimidin-4-yl)-trans-2,6-dimethylhexahydro-1H-azepine | HCID 86607464 | 100.4% |
Reaction Steps
Into 3 ml of acetonitrile were added 0.2 g of 4,6-dichloro-5-fluoropyrimidine, 0.50 g of potassium carbonate and 0.27 g of trans-2,6-dimethylhexahydro-1H-azepine hydrochloride, and the mixture was stirred for 2 hours at 60° C. The reaction mixture was cooled to near room temperature, a saturated ammonium chloride aqueous solution was added therein, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.31 g of 1-(6-chloro-5-fluoropyrimidin-4-yl)-trans-2,6-dimethylhexahydro-1H-azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732448B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-1e2a8994a3ec43769ce7ac0b6eef0f74 |
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| Source note | uspto-grants-2010_06 |
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