HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008729Generated: October 26, 2026
Potassium Carbonate → 1-(6-chloropyrimidin-4-yl)-cis-2,6-dimethylhexahydro-1H-azepine
https://huagongshe.com/reaction/1008729
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 | cis-2,6-dimethylhexahydro-1H-azepine hydrochloride | HCID 66594948 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(6-chloropyrimidin-4-yl)-cis-2,6-dimethylhexahydro-1H-azepine | HCID 86607462 | 62.1% |
Reaction Steps
Into 4 ml of acetonitrile were added 0.3 g of 4,6-dichloropyrimidine, 0.83 g of potassium carbonate and 0.43 g of cis-2,6-dimethylhexahydro-1H-azepine hydrochloride, and the mixture was stirred for 4 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 0.3 g of 1-(6-chloropyrimidin-4-yl)-cis-2,6-dimethylhexahydro-1H-azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973028B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-5e0d3251d062494bab40a5eb0d4ef864 |
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| Source note | uspto-grants-2011_07 |
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