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HRID 1931823Erstellt: 25. Oktober 2026

1-Iodopropane → (+)-3-(2,3-Difluorophenyl)-1-propylpyrrolidin-3-OL

https://huagongshe.com/reaction/1931823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-IodopropaneHCID 33643—
Edukt1-Benzyl-3-(2,3-difluorophenyl)pyrrolidin-3-olHCID 68515849—
LösungsmittelDimethylformamideHCID 6228—
Produkt(+)-3-(2,3-Difluorophenyl)-1-propylpyrrolidin-3-OLHCID 2514381334,5%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

In a sealed tube a mixture of (+)-1-benzyl-3-(2,3-difluorophenyl)pyrrolidin-3-ol (0.40 g, 1.38 mmol), dimethyl formamide (3 mL) and iodopropane (1.35 mL, 13.8 mmol) was heated under microwave irradiation at 80° C. for 45 minutes. The resulting mixture was evaporated, morpholine (2 mL) was added and the mixture was heated under micro-wave irradiation at 130° C. for 30 minutes. Aqueous sodium carbonate (10%, 50 mL) was added and the aqueous phase was extracted with ethyl acetate (2×50 mL), the combined organic phase was washed with aqueous LiCl (5%, 50 mL), dried (Na2SO4) and evaporated. Purification by HPLC on Waters OBD C18, 5 μm (MeOH/33 mM NH3, 40:60 to 60:40) gave the title compound (0.115 g). [α]D=+22.8° (methanol). The amine was converted to the fumaric acid salt and recrystallized from methanol/diethyl ether/diisopropyl ether: M.p. 95-98° C.; MS m/z (relative intensity, 70 eV) 241 (M+, 8), 212, (bp), 182 (41), 84 (88), 57 (24).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08188301B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-c802337982cd4a5694776afe5a3fc48c
Quellennotizuspto-grants-2012_05