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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1051235Erstellt: 26. Oktober 2026

Methanol → (S)-N4-(3-ethynylphenyl)-7-(tetrahydrofuran-3-yloxy)quinazoline-4,6-diamine

https://huagongshe.com/reaction/1051235

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktWaterHCID 962—
EduktAzane;hydrochlorideHCID 12820921—
Edukt(S)-N-(3-ethynylphenyl)-6-nitro-7-(tetrahydrofuran-3-yloxy)quinazolin-4-amineHCID 90014153—
KatalysatorIronHCID 23925—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(S)-N4-(3-ethynylphenyl)-7-(tetrahydrofuran-3-yloxy)quinazoline-4,6-diamineHCID 9001359948,9%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

(S)—N-(3-ethynylphenyl)-6-nitro-7-(tetrahydrofuran-3-yloxy)quinazolin-4-amine (4 g, 0.011 mol) and ammonia hydrochloride (2.4 g, 0.045 mol) was mixed in a solution of 150 mL methanol, 75 mL H2O, 50 ml EA, and then was heated to 70° C. Fe (4.8 g, 0.085 mol) was added and the reaction mixture was heated to reflux for 4 hours. The resulting reaction solution was filtered and concentrated under reduced pressure to remove most of solvent. The residue was diluted in 100 mL H2O, extracted with ethyl acetate (3×100 mL), the organic layers were concentrated to give (S)—N4-(3-ethynylphenyl)-7-(tetrahydrofuran-3-yloxy)quinazoline-4,6-diamine as grey solid 1.8 g (48.9% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09388170B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-78ad331bab724c7e9e1947e7fda91800
Quellennotizuspto-grants-2016_07