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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15960Erstellt: 25. Oktober 2026

Lithium Hexamethyldisilazide → 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridazine-3-carboxamide

https://huagongshe.com/reaction/15960

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium HexamethyldisilazideHCID 2733832—
EduktO-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
EduktMethyl 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 66673411—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridazine-3-carboxamideHCID 8660161599%

Reaktionsschritte

To a solution of methyl 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate (25 mg, 0.077 mmol) and O-(2-vinyloxy-ethyl)-hydroxylamine (24 mg, 0.23 mmol) in THF (2 mL) at 0° C. was added LiHMDS (0.54 mL, 0.54 mmol, 1 M in THF). The reaction mixture was warmed to room temperature and stirred for 1 hour. The reaction mixture was quenched with saturated aqueous NaHCO3 and diluted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude material that was purified by silica gel flash column chromatography (100% CH2Cl2 to 1.5% MeOH in CH2Cl2) to afford 30 mg (99%) of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732616B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3b25464ef122462787f2fbae1dbb57ee
Quellennotizuspto-grants-2010_06