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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 907793Erstellt: 25. Oktober 2026

Triethylamine → 3-(4-Isobutyrylpiperazine-1-carbonyl)benzaldehyde

https://huagongshe.com/reaction/907793

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-CarboxybenzaldehydeHCID 12077—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt2-Methyl-1-(piperazin-1-yl)propan-1-oneHCID 2761409—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(4-Isobutyrylpiperazine-1-carbonyl)benzaldehydeHCID 8663902899,9%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08012976B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-12f36c656e56440ab0456af098414e88
Quellennotizuspto-grants-2011_09