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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1616071Erstellt: 26. Oktober 2026

2-Amino-5-fluoro-N-methoxy-N-methylbenzamide → 3-Methylpyridine-2-carboxaldehyde

https://huagongshe.com/reaction/1616071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-5-fluoro-N-methoxy-N-methylbenzamideHCID 53407572—
EduktHCID 178418918HCID 178418918—
EduktHCID 178426302HCID 178426302—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Methylpyridine-2-carboxaldehydeHCID 1501874—

Reaktionsschritte

To a solution of 2-amino-5-fluoro-N-methoxy-N-methylbenzamide (1.0 g, 5.05 mmol) in THF (4.2 mL) was added isopropylmagnesium chloride (2.0M in THF, 5.0 mL, 10.1 mmol) at −40° C. The temperature was allowed to rise to −10° C. over 40 min then was lowered to −40° C. in an acetonitrile/dry ice bath. 3-Methyl-2-pyridinylmagnesium bromide (0.25M in THF, 20.2 mL, 5.0 mmol) was added dropwise and the solution was allowed to rise to rt over one hour. The solution was partitioned between satd ammonium chloride solution and DCM; organic extracts were concentrated then purified by silica gel column chromatography eluting with a gradient of 10-70% EtOAc in hexane to afford 2-amino-5-fluorophenyl)(3-methylpyridin-2-yl)methanone as a yellow oil: LC-MS (ESI) m/z 231.2 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08765768B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-093185e68e544071a1aec297b85ac95c
Quellennotizuspto-grants-2014_07