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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1259832Erstellt: 26. Oktober 2026

Water → Rac-2-(tert-butoxycarbonylamino-methyl)-3-(7-fluoro-2-methoxy-quinolin-8-yl)-propionic acid ethyl ester

https://huagongshe.com/reaction/1259832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktLithium HexamethyldisilazideHCID 2733832—
EduktEthyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
Edukt8-(Bromomethyl)-7-fluoro-2-(methyloxy)quinolineHCID 66737650—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktRac-2-(tert-butoxycarbonylamino-methyl)-3-(7-fluoro-2-methoxy-quinolin-8-yl)-propionic acid ethyl esterHCID 6718170175%

Reaktionsschritte

To a solution of LiHMDS (1M, 20 mL), cooled to −78° C., was added dropwise a solution of 3-tert-butoxycarbonylamino-propionic acid ethyl ester (2.01 g, 9.26 mmol; prepared according to Tetrahedron Lett. (2003), 44(14), 2807) in THF (20 mL). The solution was stirred at the same temperature for 90 min. A solution of 8-bromomethyl-7-fluoro-2-methoxy-quinoline (2.5 g, 1 eq., prepared according to WO 2007/081597) 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 separated 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 purified by CC (Hept-EA 2-1) to afford the title intermediate as a pale yellow oil which solidified after standing at rt for one day (2.83 g, 75% yield). MS (ESI, m/z): 407.3 [M+H+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08466168B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-5859d27fedf84df187a55bf7c8b9fad4
Quellennotizuspto-grants-2013_06