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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1067255Erstellt: 25. Oktober 2026

2,4,6-Trimethylpyridine → Pnu-183792

https://huagongshe.com/reaction/1067255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-TrimethylpyridineHCID 7953—
EduktMorpholineHCID 8083—
EduktMethanesulfonyl chlorideHCID 31297—
EduktN-(4-Chlorobenzyl)-6-(hydroxymethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamideHCID 15516933—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
ProduktPnu-183792HCID 49240642%

Reaktionsschritte

A solution of N-(4-chlorobenzyl)-6-(hydroxymethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide from the product of Example 2 (140 mg), collidine (0.061 mL), and DMAP (8.1 mg) in 6.7 mL anhydrous DMF is cooled to 0° C. Methanesulfonyl chloride (0.12 mL) is added dropwise. The reaction is stirred at room temperature for approx. 2-3 hrs. Morpholine (0.34 mL) is added. The product is precipitated by addition of H2O. The crude product is adsorbed onto silica and chromatographed eluting with 2% MeOH in CH2Cl2. Fractions homogenous by TLC are combined and condensed to afford 70.1 mg (42%) of the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06248736B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-afe528f57a42403bbc22a997d53feb40
Quellennotizuspto-grants-2001_06