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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-(4-Piperidinyl)-1H-indole | HCID 702235 | — |
| Edukt | 4-Oxo-3-thiazolidinylacetyl chloride | HCID 21297225 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine | HCID 21297222 | 27,5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04764514 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-0003897d204849bf86b2e0ba626abee7 |
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| Quellennotiz | uspto-grants-1988_08 |
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