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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50656Erstellt: 24. Oktober 2026

Diisopropylethylamine → [1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanone

https://huagongshe.com/de/reaction/50656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-(4-Chlorophenyl)cyclopentanecarboxylic acidHCID 97447—
EduktPiperidin-3-ylmethanolHCID 107308—
EduktPyBroPHCID 2733179—
LösungsmittelDichloromethaneHCID 6344—
Produkt[1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanoneHCID 22335026156,9%

Reaktionsschritte

A solution of piperdin-3-yl methanol (0.342 g, 2.97 mmol), 1-(4-chloro-phenyl)-cyclopentylcarboxylic acid (1.0 g, 4.45 mmol), diisopropylethyl amine (1.9, 15.00 mmol) in dichloromethane (7 mL) was stirred at room temperature. PyBroP (2.07 g, 4.45 mmol) was added and the reaction mixture continued stirring at room temperature. After 12 h the reaction mixture was quenched with 10% KOH. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to yield a crude oil. The crude material was purified using silica gel chromatography (95:5 hexane:ethyl acetate) to yield the desired compound (1.50 g). C18H24ClNO2, LRMS (m/z)=322 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713479B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-f01119f38d2b4a158dbe36d70edafa10
Quellennotizuspto-grants-2004_03