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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38249Erstellt: 23. Oktober 2026

Triethylamine → N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide

https://huagongshe.com/de/reaction/38249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPicolinoyl Chloride HydrochlorideHCID 135033—
Edukt1-(4-(4-Amino-2-chlorophenyl)piperazin-1-yl)-2-methylpropan-1-oneHCID 936926—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamideHCID 4264502518%

Reaktionsschritte

According to Scheme 4 Step 3: Picolinoyl chloride hydrochloride (0.93 mmol, 178 mg) and Et3N (1.86 mmol, 0.26 mL) were added to a solution of 1-(4-(4-amino-2-chlorophenyl)piperazin-1-yl)-2-methylpropan-1-one (0.62 mmol, 175 mg) in DCM (3 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over C18 column using water/ACN (60:40) as eluent to afford N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide (0.11 mmol, 42 mg, 18%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524726B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-bf9a8f47cc0d45d592b8c2e6d4a9879b
Quellennotizuspto-grants-2013_09