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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1820917Erstellt: 26. Oktober 2026

Hydrochloric Acid → HCID 23125711, Verbindung

https://huagongshe.com/reaction/1820917

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktThionyl ChlorideHCID 24386—
Edukt5-Methoxy-5-oxopentanoateHCID 6993194—
Edukt3-amino-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamideHCID 23062590—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelPyridineHCID 1049—
LösungsmittelChloroformHCID 6212—
ProduktHCID 23125711HCID 2312571185,2%

Reaktionsschritte

Monomethyl glutarate (3.32 g) is dissolved in chloroform (50 ml) and thereto are added thionyl chloride (1.75 ml) and N,N-dimethylformamide (one drop). After stirring for 1.5 hours at the same temperature, the reaction solution is cooled, and thereto are added 3-amino-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide (5.00 g) obtained in Reference Example 80 and pyridine (7.0 ml). After stirring for 2.5 hours at room temperature, the reaction solution is poured into 5% hydrochloric acid and extracted with chloroform. The organic layer is washed successively with saturated brine, a saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate, and evaporated to remove the solvent under reduced pressure. The resulting residue is suspended in diisopropyl ether and the precipitates are collected by filtration to give methyl 5-[(2-{[(5-chloropyridin-2-yl)amino]carbonyl}benzofuran-3-yl)amino]-5-oxopentanoate (6.16 g). APCI-MS M/Z:416/418[M+H]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07605158B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-c3542a4506fc4137b0d2af184aa3883b
Quellennotizuspto-grants-2009_10