Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2214833Erstellt: 25. Oktober 2026

p-Bromobenzenesulfonyl chloride → 4-(4-Bromobenzenesulfonyl)-1-{[4-ethoxycarbonylamino-1-(2-methyl-4-pyridyl)-4-piperidinyl]methyl}-2-piperazinone

https://huagongshe.com/reaction/2214833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Bromobenzenesulfonyl chlorideHCID 7396—
EduktTriethylamineHCID 8471—
EduktSodium CarbonateHCID 10340—
EduktHCID 21948312HCID 21948312—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(4-Bromobenzenesulfonyl)-1-{[4-ethoxycarbonylamino-1-(2-methyl-4-pyridyl)-4-piperidinyl]methyl}-2-piperazinoneHCID 1021066767,9%

Reaktionsschritte

Triethylamine (400 mg) was added to a solution of 1-{[4-ethoxycarbonylamino-1-(2-methyl-4-pyridyl)-4-piperidinyl]methyl}-2-piperazinone hydrochloride (440 mg) obtained in Reference Example 11 in dichloromethane (15 ml), 4-bromobenzenesulfonyl chloride (255 mg) was added at 0° C., and the mixture was stirred at room temperature for 1 hour. An aqueous sodium carbonate solution was added to the reaction solution, the material was extracted with dichloromethane, dried, concentrated, and purified by silica gel column chromatography (dichloromethane:10% aqueous ammonia-containing methanol=20:1) to obtain the title compound (403 mg) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07109200B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-a2eb2c7174664d53ad8e435e13acf648
Quellennotizuspto-grants-2006_09