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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 509960Erstellt: 27. Oktober 2026

sodium thiosulfite anhydrous → 6-[(5-Fluoro-2-methoxy-pyridin-3-ylmethyl)-amino]-pyridine-3-carbaldehyde

https://huagongshe.com/reaction/509960

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktsodium thiosulfite anhydrousHCID 15847209—
Edukt{6-[(5-Fluoro-2-methoxy-pyridin-3-ylmethyl)-amino]pyridin-3-yl}-methanolHCID 58259120—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-[(5-Fluoro-2-methoxy-pyridin-3-ylmethyl)-amino]-pyridine-3-carbaldehydeHCID 86653326—

Reaktionsschritte

To {6-[(5-fluoro-2-methoxy-pyridin-3-ylmethyl)-amino]-pyridin-3-yl}-methanol (92, 0.353 g, 1.34 mmol) dissolved in 8 mL of tetrahydrofuran, Dess-Maritn periodinane (0.626 g, 1.47 mmol) was added and the reaction stirred at room temperature for 1 hour. The reaction was poured into aqueous saturated sodium thiosulfite and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography eluting with ethyl acetate and hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound. MS (ESI) [M+H+]+=262.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096593B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-510c1f871672421eba91ddc709628ff1
Quellennotizuspto-grants-2015_08