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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238997Erstellt: 24. Oktober 2026

2,3-Dihydroxybutanedioic Acid → Erlotinib Hydrochloride

https://huagongshe.com/de/reaction/238997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dihydroxybutanedioic AcidHCID 875—
EduktBenzenamine, 3-ethynyl-HCID 104682—
Edukt4-Chloro-6,7-bis(2-methoxyethoxy)quinazolineHCID 11289942—
LösungsmittelEthanolHCID 702—
ProduktErlotinib HydrochlorideHCID 176871—

Reaktionsbedingungen

Temperatur27.5 °C

Reaktionsschritte

15.0 g of 4-chloro-6,7-bis(2-methoxyethoxy) quinazoline was suspended in 450 ml ethanol and 13.8 g of 3-aminophenyl acetylene was added at 25-30° C. Further 3.0 g tartaric acid was added. The reaction mass was stirred at 25-30° C. for 6 hours. Solid obtained was filtered, washed with water and dried under vacuum. This solid was suspended in water, basified with potassium hydroxide and stirred for 10 minutes. The resulting erlotinib base was isolated by filtration, washed with ethanol and dried under vacuum. The solid obtained was then suspended in water and acidified to pH 1.0-2.0 using hydrochloric acid. The reaction mixture was stirred for 2 hours, filtered, washed with water and dried at 40-45° C. to obtain 18.3 g of erlotinib hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642758B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-4cdbc0085e5e4bffada7bdf44fc86788
Quellennotizuspto-grants-2014_02