HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216019Erstellt: 25. Oktober 2026
Dicyclohexylcarbodiimide → Tert-butyl 4-(3-(4-fluorophenoxy)phenylcarbamoyl)-4-methylpiperidine-1-carboxylate
https://huagongshe.com/reaction/216019
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | HOAt | HCID 181649 | — |
| Edukt | 1-[(Tert-butoxy)carbonyl]-4-methylpiperidine-4-carboxylic acid | HCID 23282848 | — |
| Edukt | 3-(4-Fluorophenoxy)aniline | HCID 23506015 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Tert-butyl 4-(3-(4-fluorophenoxy)phenylcarbamoyl)-4-methylpiperidine-1-carboxylate | HCID 68989388 | — |
Reaktionsschritte
1-(tert-butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid (243 mg, 1.0 mmol), 3-(4-fluorophenoxy)aniline (203 mg, 1.0 mmol), DCC (206 mg, 1.0 mmol), and HOAt (138 mg, 1.01 mmol) were combined in EtOAc (50 mL) and DMF (5 mL). The reaction mixture was heated at 80° C. for 20 hours. Most of the EtOAc was evaporated, resulting in precipitation of a solid, which was removed by filtration. The filtrate was diluted with EtOAc, washed with 1 N aq. HCl, water, and brine, dried, and concentrated under vacuum to give the title compound. MS (ES+) [M+H]+=429.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08193202B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-6984cfa846b849f798264fda96d7ebfc |
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| Quellennotiz | uspto-grants-2012_06 |
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