HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384698Erstellt: 25. Oktober 2026
Triethylamine → Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/384698
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Aminomethyl-1-N-Cbz-piperidine | HCID 21955499 | — |
| Edukt | N-(5-bromo-4-chloropyridin-2-yl)-2,2-dimethylpropanamide | HCID 59613421 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylate | HCID 59613492 | 87,2% |
Reaktionsschritte
Two capped microwave reaction vials each containing a solution of N-(5-bromo-4-chloropyridin-2-yl)pivalamide (0.55 g, 1.89 mmol), benzyl 4-(aminomethyl)piperidine-1-carboxylate (1.07 g, 2 eq.) and triethylamine (0.80 mL, 3 eq.) in NMP (3.8 mL) were heated at 210° C. by microwave irradiation for 1.5 hr and then allowed to cool. The contents of the two vials were combined and partitioned between EtOAc (15 mL) and sat. NaHCO3 (150 mL). The organic layer was retained whilst the aqueous was further extracted with EtOAc (15 mL). The organic extracts were combined, washed with brine (50 mL), dried (MgSO4) and concentrated. The crude material was purified by chromatography on a 40+M Biotage silica column, eluting with a gradient of EtOAc in dichloromethane, to give the title compound as a clear oil (0.83 g, 43%)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367658B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-a00b10751029486d80d9e3dfdd8c6e3b |
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| Quellennotiz | uspto-grants-2013_02 |
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