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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34910Erstellt: 24. Oktober 2026

Triethylamine → 4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine

https://huagongshe.com/de/reaction/34910

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-(4-Piperidinyl)-1H-indoleHCID 702235—
Edukt4-Oxo-3-thiazolidinylacetyl chlorideHCID 21297225—
LösungsmittelChloroformHCID 6212—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidineHCID 2129722227,5%

Reaktionsschritte

A solution of 4-oxo-3-thiazolidinylacetyl chloride (1.75 g) in tetrahydrofuran (5.00 ml) was added dropsise to a suspension of 3-(4-piperidyl)indole (2.00 g) and triethylamine (4.10 ml) in a mixture of tetrahydrofuran (15.0 ml) and chloroform (5.00 ml) at 4° to 7° C. with stirring. After the mixture was allowed to stir for 1 hour with ice-bath cooling, the resultant precipitate was removed by filtration and the solvent was evaporated in vacuo. The residue was mixed with saturated aqueous sodium hydrogen carbonate (10.0 ml) and the mixture was extracted with chloroform (20.0 ml). The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of methanol and acetone to give 4-(3-indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine (0.92 g) as slightly brown prisms.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04764514
Quelldatensatzuspto-grants-1988_08
ORD IDord-0003897d204849bf86b2e0ba626abee7
Quellennotizuspto-grants-1988_08