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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346414Erstellt: 25. Oktober 2026

Ethanol → 4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-aminoquinazoline

https://huagongshe.com/reaction/346414

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktIsopropanolHCID 3776—
EduktHydrazine hydrate (1:1)HCID 24654—
Edukt4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-nitroquinazolineHCID 15480998—
KatalysatorNickelHCID 935—
LösungsmittelWaterHCID 962—
Produkt4-[(3,4-Dichloro-6-fluorophenyl)amino]-6-aminoquinazolineHCID 11544325—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A solution of 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-nitroquinazoline (709 mg, 2.076 mmol) in 140 ml of 1:9:10 water:ethanol:iso-propylalcohol was heated to reflux temperature (95° C.). Additional 60 ml of the solvents mixture was added until complete dissolution. The reaction mixture was then cooled to 65° C., and 200 μl hydrazine hydrate (4.12 mmol) and 0.5 ml Raney®Nickel (in water) were added subsequently thereto. The resulting mixture was heated up to 80–85° C., additional 0.5 ml Raney®Nickel and 50 μl of hydrazine hydrate (1.03 mmol) were added, and gentle reflux was maintained for about 15–20 minutes. Filtration and evaporation gave 4-[(3,4-dichloro-6-fluorophenyl)amino]-6-aminoquinazoline (compound 2) in 83% yield. m.p.=265° C.; MS (m/z): 323.4, 325.4 (M+); Anal. calcd.: C, 52.9; H, 2.78; N, 17.33. Found: C, 52.19; H, 2.99; N, 17.14. HPLC analysis. C-18 column, 55% acetate buffer, PH=3.8/45% acetonitrile, flow=1 ml/min; r.t=6.6 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07172749B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-27cadef5d46d497385dc647efc143730
Quellennotizuspto-grants-2007_02