HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1801471Erstellt: 26. Oktober 2026
Water → Rac-2-(tert-butoxycarbonylamino-methyl)-3-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-propionic acid ethyl ester
https://huagongshe.com/reaction/1801471
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Edukt | Ethyl 3-{[(tert-butoxy)carbonyl]amino}propanoate | HCID 15933116 | — |
| Edukt | 8-Bromomethyl-7-fluoro-2-methoxy-[1,5]naphthyridine | HCID 67223878 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Rac-2-(tert-butoxycarbonylamino-methyl)-3-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-propionic acid ethyl ester | HCID 67181383 | 75% |
Reaktionsschritte
To a solution of LiHMDS (1M, 17 mL, 2.2 eq.), cooled to −78° C., was added dropwise a solution of 3-tert-butoxycarbonylamino-propionic acid ethyl ester (1.70 g, 7.82 mmol, prepared according to Tetrahedron Lett. (2003), 44, 2807-2811) in THF (20 mL). The solution was stirred at the same temperature for 90 min. A solution of 8-bromomethyl-7-fluoro-2-methoxy-[1,5]naphthyridine (2.12 g, 1 eq., prepared according to WO 2008/078305) in THF (10 mL) was quickly added and the reaction proceeded 2 h, keeping the internal temperature below −50° C. Water (100 mL) and EA (200 mL) were added. The two layers were decanted and the aq. layer was extracted with EA. The combined org. layers were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was chromatographed (Hept-EA 2-1) to afford the title intermediate as a yellow oil (2.38 g, 75% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08349828B2 |
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| Quelldatensatz | uspto-grants-2013_01 |
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| ORD ID | ord-7664b219bb7d48a3a80515b374aa490c |
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| Quellennotiz | uspto-grants-2013_01 |
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