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HRID 911301Erstellt: 24. Oktober 2026
Sodium Azide → 2-Pyridinemethanamine, 5-(2,2,2-trifluoroethoxy)-
https://huagongshe.com/de/reaction/911301
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Azide | HCID 33557 | — |
| Edukt | Pyridine, 2-(bromomethyl)-5-(2,2,2-trifluoroethoxy)- | HCID 57655951 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Pyridinemethanamine, 5-(2,2,2-trifluoroethoxy)- | HCID 57656092 | 54,6% |
Reaktionsschritte
Dissolve sodium azide (270 mg, 4.0 mmol) in DM (30 mL). Cool the solution to 0° C., then add 2-bromomethyl-5-(2,2,2-trifluoroethoxy)-pyridine (440 mg, 1.6 mmol) at 0° C. Slowly heat the mixture from 0° C. to 80° C. over 30 min. Cool the reaction, dilute with EtOAc (100 mL) and wash with 10% aqueous NaCl (3×25 mL). Collect the organic layer and concentrate in vacuo to a volume of 50 mL. Transfer the solution to a pressure vessel. Add 10% Pd/C (Degussa type E101, 50% water by wt, 500 mg) and pressurize the vessel under hydrogen (10 psi) for 1 h with stirring. Filter the mixture through Celite® and wash filter cake with warm methanol followed by DCM. Concentrate in vacuo, then purify by chromatography on silica gel eluting with DCM/2M ammonia in methanol (20:1) to obtain the title compound (180 mg, 54%). MS (ES+) m/z: 207 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08022062B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-8c7ec263325740aa99b5dd2952665214 |
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| Quellennotiz | uspto-grants-2011_09 |
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