HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278235Erstellt: 26. Oktober 2026
Ammonium Chloride → Tert-butyl 4-(2H-tetrazol-5-YL)piperidine-1-carboxylate
https://huagongshe.com/reaction/278235
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Sodium Azide | HCID 33557 | — |
| Edukt | Tert-butyl 4-cyanopiperidine-1-carboxylate | HCID 1514443 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Tert-butyl 4-(2H-tetrazol-5-YL)piperidine-1-carboxylate | HCID 18187701 | 60% |
Reaktionsschritte
A mixture of 2.10 g (10.0 mmol) of 1-(t-butoxycarbonyl)-4-cyanopiperidine (from Step A), 1.95 g (30.0 mmol) of sodium azide and 1.60 g (30.0 mmol) of ammonium chloride in 20 mL of DMF was stirred at 100° C. for 20 h. The mixture was cooled and partitioned between 200 mL of methylene chloride and 200 mL of 1.0 N HCl and the layers were separated. The organic layer was washed with 200 mL of water, dried over magnesium sulfate and concentrated. Flash chromatography on 50 g of silica gel using 4:1 v/v methylene chloride/ethyl acetate+1% acetic acid, then 2:1 v/v methylene chloride/ethyl acetate+1% acetic acid as the eluent afforded 1.51 g (60%) of the title compound:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06358979B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-204f252feebe4f45bd2e18f59a724327 |
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| Quellennotiz | uspto-grants-2002_03 |
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