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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1017453Erstellt: 27. Oktober 2026

Dimethylformamide → 2-(3,5-Dimethoxy-phenyl)-N-methyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-acetamide

https://huagongshe.com/reaction/1017453

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt(3,5-Dimethoxyphenyl)acetic acidHCID 138316—
EduktMethyl-(6-morpholin-4-yl-4-tolyl-pyridin-3-yl)-amineHCID 69138572—
Produkt2-(3,5-Dimethoxy-phenyl)-N-methyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-acetamideHCID 993400975%

Reaktionsschritte

To a solution of 226 mg (1.15 mmol) 3,5-dimethoxy-phenylacetic acid in 7 ml N,N-dimethylformamide were added 244 mg (1.5 mmol) 1,1′-carbonyl-diimidazole and the solution was stirred for 30 min at room temperature. After addition of 283 mg (1 mmol) of methyl-(6-morpholin-4-yl-4-tolyl-pyridin-3-yl)-amine (as described in step f) for the preparation of Example 23), the reaction mixture was heated at 70° C. for 7 h. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved in 30 ml ethyl acetate. The organic phase was washed with water (2×30 ml), brine, dried (magnesium sulfate) and evaporated. Flash chromatography gave 347 mg (75%) of the title compound as a white foam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06479483B2
Quelldatensatzuspto-grants-2002_11
ORD IDord-9e2d9c65404243dbbd4c834c70325c08
Quellennotizuspto-grants-2002_11