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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16692Erstellt: 23. Oktober 2026

Hydrochloric Acid → HCID 178426582, Verbindung

https://huagongshe.com/de/reaction/16692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-Amino-5-methylpyridineHCID 15348—
EduktSodium BicarbonateHCID 516892—
EduktTrimethylaluminum hexaneHCID 86584505—
EduktHCID 178499199HCID 178499199—
LösungsmittelChloroformHCID 6212—
ProduktHCID 178426582HCID 17842658261,6%

Reaktionsschritte

2-Amino-5-methylpyridine (81 mg) is dissolved in chloroform (5 ml). After adding 0.98 M trimethyl aluminum-hexane solution (763 μl) under ice-cooling, the reaction solution is stirred under ice-cooling for 10 minutes, and then at room temperature for 0.5 hours. To the resulting reaction solution is added methyl 3-({[trans-4-(3-oxomorpholin-4-yl)cyclohexyl]carbonyl}amino)furo[3,2-b]pyridine-2-carboxylate (150 mg) obtained in Reference Example 79, and the mixture is stirred at room temperature for 2 hours and at 50° C. under heating for 5 hours. To the reaction solution is added 10% hydrochloric acid (3 ml) under ice-cooling, and the mixture is stirred at room temperature for 0.5 hours. The reaction solution is then neutralized by adding saturated aqueous sodium hydrogen carbonate solution, and extracted with chloroform. The organic layer is washed with saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by NH-silica gel column chromatography (eluent: ethyl acetate followed by ethyl acetate/methanol=10/1). The resulting solid is suspended in diethyl ether, and collected by filtration to give the title compound (110 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737161B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-eae17f8ebaf8493a9c5aabf38ce0cd74
Quellennotizuspto-grants-2010_06