HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608650Generated: October 30, 2026
Potassium Carbonate → HCID 53896186, compound
https://huagongshe.com/reaction/1608650
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, (3-chloro-1-propenyl)- | HCID 94242 | — |
| Reactant | HCID 5298668 | HCID 5298668 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53896186 | HCID 53896186 | 49% |
Reaction Steps
0.75 g (3.3 mmoles) of 4-chloro-2-methyl-5-(1-piperazinyl)-3(2H)-pyridazinone prepared as described hereinafter under the title "Preparation of the starting substances" and 0.91 g (6.6 mmoles) of anhydrous potassium carbonate are suspended in 5 ml of anhydrous dimethyl formamide. Then a solution of 0.5 g (3.3 moles) of 3-phenyl-2-propenyl chloride in 5 ml of anhydrous dimethyl formamide are dropped to the suspension, and the reaction mixture is stirred at room temperature for 24 hours. The dimethyl formamide is evaporated in vacuo, a slight amount of water is added to the residue and the solution thus obtained is extracted with ethyl acetate. The organic phase is dried and evaporated and the residue is crystallized from ethanol. Thus 0.55 g (49%) of the desired compound is obtained. M.p.: 98°-100° C. Its monohydrochloride salt melts at 218°-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05395934 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-9c5df838263b40bd825c8dd0dfe264f6 |
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| Source note | uspto-grants-1995_03 |
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