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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38251Erstellt: 24. Oktober 2026

Triethylamine → Tert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/38251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPicolinoyl Chloride HydrochlorideHCID 135033—
EduktTert-Butyl 4-(4-Amino-2-Chlorophenyl)Piperazine-1-CarboxylateHCID 18783766—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylateHCID 67441071100%

Reaktionsschritte

According to Scheme 5 Step 3: Picolinoyl chloride hydrochloride (3.68 mmol, 656 mg) and Et3N (7.37 mmol, 1.03 mL) were added to a solution of tert-butyl 4-(4-amino-2-chlorophenyl)piperazine-1-carboxylate (2.46 mmol, 766 mg) in DCM (40 mL) at 0° C. The reaction mixture was stirred at room temperature for 1 hour. 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 to afford tert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylate (2.46 mmol, 1.02 g, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524726B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-fbce41f4d7ee430591e03e6b74442165
Quellennotizuspto-grants-2013_09