HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1162335Erstellt: 25. Oktober 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 178433047, Verbindung
https://huagongshe.com/reaction/1162335
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | tert-Butyl 4-(2-hydroxyethylamino)piperidine-1-carboxylate | HCID 23131007 | — |
| Edukt | HCID 178433052 | HCID 178433052 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 178433047 | HCID 178433047 | 18% |
Reaktionsschritte
2-Methylimidazole-4-carboxylic acid (2.0 g) was suspended in acetonitrile (150 ml). HOBt (3.7 g) and WSC (4.6 g) were sequentially added thereto, and then mixed at room temperature for 20 minutes. To the reaction solution was added a solution of tert-butyl 4-(2-hydroxyethyl)amino-1-piperidinecarboxylate (4.7 g) obtained in Example 91a) and triethylamine (8.0 ml) in acetonitrile (50 ml), and mixed at room temperature for 15 hours. Acetonitrile was distilled off under reduced pressure, and then to the residue were added chloroform and water. The organic layer was collected by separation and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified with basic silica gel column (ethyl acetate:ethanol=5:1) to obtain the title compound as a colorless oil (1.0 g, 18%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07820673B2 |
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| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-06869875e4ca49cf8372c3e6c6c2ff19 |
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| Quellennotiz | uspto-grants-2010_10 |
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