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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16775Erstellt: 24. Oktober 2026

Pyridine → Methyl 4-(4-methylpiperazine-1-carbonyl)benzoate

https://huagongshe.com/de/reaction/16775

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktMonomethyl terephthalateHCID 15513—
Edukt1-MethylpiperazineHCID 53167—
EduktOxalyl chlorideHCID 65578—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-(4-methylpiperazine-1-carbonyl)benzoateHCID 1717822367,9%

Reaktionsschritte

Oxalyl chloride (0.533 mL, 6.11 mmol) was added dropwise to a stirred suspension of 4-(methoxycarbonyl)benzoic acid (1 g, 5.55 mmol) in DCM (20 mL) under nitrogen. The resulting suspension was stirred at room temperature for 30 mins. DMF (0.05 mL) was added dropwise under nitrogen. The resulting suspension was stirred for 90 mins. A solution of 1-methylpiperazine (0.554 mL, 5.00 mmol) and pyridine (1.211 mL, 14.99 mmol) in DCM (15 mL) was added dropwise at 0° C., over a period of 60 mins under nitrogen. The resulting solution was stirred at room temperature for 3 h. The reaction mixture was evaporated to dryness to afford the crude product (1.791 g) as a dark orange solid. The solid was redissolved in DCM and washed with NaHCO3. The organic layer was evaporated to dryness to afford methyl 4-(4-methylpiperazine-1-carbonyl)benzoate (0.890 g, 61.1%) as an orange gum, which solidified on standing. Used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-fb35064d694440779fad2aeb07bf3334
Quellennotizuspto-grants-2010_06