HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 333960Erstellt: 24. Oktober 2026
tert-Butyl piperazine-1-carboxylate → (8-Methyl-4-quinolyl)piperazine
https://huagongshe.com/de/reaction/333960
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 4-Chloro-8-methylquinoline | HCID 12326335 | — |
| Lösungsmittel | 3-(3-Methoxypropoxy)-1-propanol | HCID 66984 | — |
| Produkt | (8-Methyl-4-quinolyl)piperazine | HCID 43840508 | 80% |
Reaktionsschritte
8-Methyl-4-chloroquinoline (355 mg, 2 mmol) was suspended in dipropyleneglycolmonomethylether (4 ml), a solution of tert-butyl piperazine-1-carboxylate (440 mg, 2.4 mmol) in dipropyleneglycolmonomethylether (4 ml) was added and the mixture was stirred at 140° C. overnight and the solvent was evaporated under reduced pressure. The residue was dissolved in a mixture of dichloromethane and trifluoroacetic acid (1:1, 4 ml) and stirred at room temperature for 90 minutes. The mixture was evaporated to dryness under reduced pressure and the residue was dissolved in dichloromethane. The solution was washed with 5% sodium bicarbonate solution and water, dried over sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by column chromatography (prepacked silica column, gradient ethyl acetate/methanol with the addition of 1% ammonia) to yield 364 mg of a solid (1.6 mmol, 80%). MS (APCI): m/z=227.9 [M+1]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08883791B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-b009f21a1158469280fafeb63b31bca4 |
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| Quellennotiz | uspto-grants-2014_11 |
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