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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279352Erstellt: 25. Oktober 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-(4-Chlorobenzyl)-3-[(4-benzoylbutyryl)amino]homopiperidine

https://huagongshe.com/reaction/279352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Eduktdelta-Oxobenzenepentanoic acidHCID 73914—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 18426239—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt1-(4-Chlorobenzyl)-3-[(4-benzoylbutyryl)amino]homopiperidineHCID 9823008—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A solution of 3-amino-1-(4-chlorobenzyl)homopiperidine (24 mg, 0.10 mmol) and 4-benzoylbutyric acid (1.2 equiv.) in CHCl3 (1 mL) was treated with EDCI (23 mg), HOBt (16.2 mg) and Et3N (15.2 μL), and stirred at 25° C. for 16 h. The reaction mixture was diluted with CH2Cl2 (0.5 mL), washed with 2 N aqueous NaOH solution (2×0.75 mL), dried by filtration through a PTFE membrane and concentrated to afford 1-(4-chlorobenzyl)-3-[(4-benzoylbutyryl)amino}homopiperidine (compound No. 994) (43 mg, 99%): The purity was determined by RPLC/MS (98%); ESI/MS m/e 413 (M++H, C24H29ClN2O2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06362177B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-e90615f838734037a6c71d400c1016f1
Quellennotizuspto-grants-2002_03