HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 337414Erstellt: 24. Oktober 2026
Dimethylformamide → 1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide
https://huagongshe.com/de/reaction/337414
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 1-Carbobenzoxy-4-piperidinecarboxylic Acid | HCID 736489 | — |
| Edukt | 2-Amino-4-(2-furyl)-5-morpholinothiazole | HCID 23144158 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide | HCID 23144107 | 100% |
Reaktionsschritte
1-Benzyloxycarbonylpiperidine-4-carboxylic acid (5.00 g, 19.0 mmol) was dissolved in dichloromethane (80 mL), and thionyl chloride (6.93 mL, 95.0 mmol) and DMF (0.15 mL, 1.90 mmol) were added thereto, followed by stirring under heating and reflux for 3 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was dissolved in dichloromethane (2 mL). The resulting solution was added to a solution of 2-amino-4-(2-furyl)-5-morpholinothiazole (2.01 g, 8.00 mmol) in pyridine (32 mL) obtained in Step 1 of Example 29, and then N,N-dimethylaminopyridine (97.6 mg, 0.800 mmol) was added thereto, followed by stirring at room temperature for 1 hour. The solvent was distilled away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=1:1 to 1:3) to afford the entitled Compound 43 (4.96 g, 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889718B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-380679c20ae54fde87e24276a7e48ec9 |
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| Quellennotiz | uspto-grants-2014_11 |
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