HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 907793Erstellt: 25. Oktober 2026
Triethylamine → 3-(4-Isobutyrylpiperazine-1-carbonyl)benzaldehyde
https://huagongshe.com/reaction/907793
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Carboxybenzaldehyde | HCID 12077 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | 2-Methyl-1-(piperazin-1-yl)propan-1-one | HCID 2761409 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(4-Isobutyrylpiperazine-1-carbonyl)benzaldehyde | HCID 86639028 | 99,9% |
Reaktionsschritte
To a solution of 3-formylbenzoic acid (750 mg, 5 mmol) in anhydrous dichloromethane (15 mL) was added triethylamine (1.263 g, 12.5 mmol), 1-hydroxybenzotriazole (0.743 g, 5.5 mmol), followed by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.05 g, 5.5 mmol). After the addition, the mixture was stirred at room temperature for 40 mins. Then the mixture was cooled to 0° C., and 2-methyl-1-(piperazin-1-yl)propan-1-one (1.06 g, 5.5 mmol) was added portionwise. After the addition, the mixture was stirred at room temperature overnight. The mixture was diluted with dichloromethane (50 mL), washed with saturated sodium bicarbonate (50 mL×2), 10% citric acid (50 mL), brine (30 mL), dried over anhydrous sodium sulfate, and concentrated to give 3-(4-isobutyrylpiperazine-1-carbonyl)benzaldehyde (1.44 g, yield: 95%) as a gum. LC-MS (ESI) m/z: 289(M+1)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08012976B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-12f36c656e56440ab0456af098414e88 |
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| Quellennotiz | uspto-grants-2011_09 |
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