HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076901Generated: October 25, 2026
Potassium Carbonate → 1-(6-chloropyrimidin-4-yl)-trans-2,6-dimethylhexahydro-1H-azepine
https://huagongshe.com/reaction/2076901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | trans-2,6-dimethylhexahydro-1H-azepine hydrochloride | HCID 66594500 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(6-chloropyrimidin-4-yl)-trans-2,6-dimethylhexahydro-1H-azepine | HCID 86607465 | 93.2% |
Reaction Steps
Into 3 ml of acetonitrile were added 0.2 g of 4,6-dichloropyrimidine, 0.56 g of potassium carbonate and 0.31 g of trans-2,6-dimethylhexahydro-1H-azepine hydrochloride, and the mixture was stirred for 2 hours at 6° 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 0.30 g of 1-(6-chloropyrimidin-4-yl)-trans-2,6-dimethylhexahydro-1H-azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928110B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-64a72597ebe5427e8f0db6561d7eb640 |
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| Source note | uspto-grants-2011_04 |
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