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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2265958Erstellt: 26. Oktober 2026

4-Methylmorpholine → HCID 74382384, Verbindung

https://huagongshe.com/reaction/2265958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrateHCID 23149411—
Edukt3-(2-Diethylamino-6-trifluoromethyl-pyridin-3-yl)-acrylic acidHCID 68782284—
Edukt3-Ethynyl-5-fluoro-4-methansulfonylaminobenzylamine hydrochlorideHCID 86625519—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 74382384HCID 7438238483,3%

Reaktionsschritte

To a suspension of N-(4-aminomethyl-2-ethynyl-6-fluoro-phenyl)-methanesulfonamide HCl salt (476 mg, 1.66 mmol) in THF (5 mL) was added N-methylmorpholine (0.365 ml, 3.32 mmol). The mixture was stirred for 5 minutes, to which were added 3-(2-diethylamino-6-trifluoromethyl-pyridin-3-yl)-acrylic acid (434 mg, 1.51 mmol) and 4-(4,6-dimethoxy[1,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (DMTMM, 459 mg, 1.66 mmol). The mixture was stirred overnight at room temperature and was concentrated under reduced pressure. The residue was diluted with EtOAc and water. The organic layer was washed with saturated sodium bicarbonate, 1N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by recrystallization from CH2Cl2 to give the title compound (645 mg, 83%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07858621B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-131de14a8331421d977fd6a05c13f4b8
Quellennotizuspto-grants-2010_12