HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380526Generated: November 3, 2026
Potassium Carbonate → HCID 23325341, compound
https://huagongshe.com/reaction/1380526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | Magnesium orthosilicate | HCID 66225 | — |
| Reactant | HCID 13686022 | HCID 13686022 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23325341 | HCID 23325341 | 30.1% |
Reaction Steps
A mixture of 5.6 g (0.02 moles) of 2-(1-piperazinyl)-7-(4-pyridyl)[1,2,4]triazolo[1,5-a]pyrimidine (prepared as described in Example 47), 3.0 g (0.02 moles) of 4-bromobutyronitrile, 4.0 g of potassium carbonate and 50 ml of N,N-dimethylformamide was heated at reflux for 16 hours with stirring. The mixture was cooled and filtered. The filter was washed with N,N-dimethylformamide and the combined filtrate and wash was evaporated in vacuo to give a dark syrup. The syrup was dissolved in chloroform and passed through a pad of magnesium silicate washing with chloroform. The filtrate was evaporated to a syrup and crystallized from ethanol/ether. The precipitate was collected by filtration and washed with ether and gave 2.1 g of the desired product as golden crystals, mp 147°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04582833 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-3754cd183b8e4ce6bd08d089d3970db3 |
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| Source note | uspto-grants-1986_04 |
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