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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktLithium HexamethyldisilazideHCID 2733832—
EduktEthyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
Edukt8-Bromomethyl-7-fluoro-2-methoxy-[1,5]naphthyridineHCID 67223878—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktRac-2-(tert-butoxycarbonylamino-methyl)-3-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-propionic acid ethyl esterHCID 6718138375%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08349828B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-7664b219bb7d48a3a80515b374aa490c
Quellennotizuspto-grants-2013_01