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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226456Erstellt: 26. Oktober 2026

Sodium Chloride → ethyl (2E)-3-(6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-fluoro-3-pyridinyl)acrylate

https://huagongshe.com/reaction/226456

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktSodium hydrideHCID 24758—
EduktEthyl (dimethoxyphosphinoyl)acetateHCID 67555—
Edukt6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-fluoronicotinaldehydeHCID 86603756—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produktethyl (2E)-3-(6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-fluoro-3-pyridinyl)acrylateHCID 8660376236%

Reaktionsbedingungen

Temperatur24 °C

Reaktionsschritte

To an ice-cooled suspension of sodium hydride (38.5 mg) in THF (10 ml) was added ethyl (dimethoxyphosphoryl)acetate (206 mg), and the mixture was stirred at 24° C. for 40 minutes. To the mixture was added 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-fluoronicotinaldehyde (250 mg) at 24° C., the reaction mixture was stirred at same temperature for 30 minutes. The reaction mixture was poured into a mixture of AcOEt and 5% aqueous NaCl. The separated organic layer was washed with brine, dried over sodium sulfate and evaporated in vacuo. The resulting residue was purified by column chromatography on silica gel (8.2 g) using a mixed solvent of CH2Cl2 and MeOH(100:1 to 35:1). The fractions containing the objective compound were collected and evaporated under reduced pressure. Title compound (111 mg, 36%) was obtained as oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557127B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-53aa52e0cdf54b7fb1370e648422767d
Quellennotizuspto-grants-2009_07