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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 558164Erstellt: 25. Oktober 2026

Methanesulfonic Acid → (S)-3-[4-(3-fluorobenzyloxy) benzylamino]pyrrolidin-2-one

https://huagongshe.com/reaction/558164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
Edukt4-[(3-Fluorophenyl)methoxy]benzaldehydeHCID 880119—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt(3S)-3-aminopyrrolidin-2-oneHCID 12430456—
LösungsmittelMethanolHCID 887—
Produkt(S)-3-[4-(3-fluorobenzyloxy) benzylamino]pyrrolidin-2-oneHCID 54532112—

Reaktionsschritte

To a 2M solution of (S)-3-aminopyrrolidin-2-one (1.47 g, 14.6 mmol), prepared as described in Example 5, in anhydrous methanol 2.0 g of 3 Å molecular sieves and 0.77 g NaBH3CN (12 mmol) were added; after 10 minutes, 3.4 g (14.8 mmol) of 4-(3-fluorobenzyloxy)benzaldehyde in 40 ml of anhydrous methanol were added. The reaction was carried out for 3 hours, then the mixture filtered, the solution was evaporated yielding a residue which was directly flash-chromatographed on silica gel (eluant: CHCl3:CH3OH:NH3 (30%) 97:3:0.3, v:v:v) to give a white solid (3.4 g; 74%). The free base thus obtained was treated with a stoichiometric amount of methanesulfonic acid to give the title compound m.p. 140.5-143.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063039B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-a96668a128a64b0b8680f1fb3af5ecf8
Quellennotizuspto-grants-2011_11