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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397663Erstellt: 25. Oktober 2026

4-Fluorobenzenesulfonyl chloride → (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid

https://huagongshe.com/reaction/397663

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluorobenzenesulfonyl chlorideHCID 9588—
EduktN,N-Diethyl-2-propanamineHCID 521913—
Edukt(2S)-2-Piperidinecarboxylic acid L-tartrateHCID 69946027—
LösungsmittelAcetoneHCID 180—
LösungsmittelSodium HydroxideHCID 14798—
Produkt(2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acidHCID 76866296,1%

Reaktionsschritte

(2S)-2-Piperidinecarboxylic acid L-tartrate (10 g) [see Preparation 1] was dissolved in 1N aqueous sodium hydroxide solution (107.4 ml) and diethylisopropylamine (9.35 ml) was added followed by a solution of 4-fluorobenzenesulphonyl chloride (10.45 g) in acetone (107 ml) at 0° C. The reaction mixture was warmed to room temperature and stirred for 18 hours after which time the solvent was removed under reduced pressure and the residue diluted with 1N aqueous sodium hydroxide solution. The aqueous solution was washed with diethyl ether and acidified with concentrated hydrochloric acid. The product was extracted with ethyl acetate, the organic layers dried over magnesium sulphate and the solvent was removed under reduced pressure to afford (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid (9.89 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610707B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-870f1d9bb4b247fbb5b6db8f1ee452a0
Quellennotizuspto-grants-2003_08