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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217137Erstellt: 24. Oktober 2026

Chloranil → 6-Nitro-2-(1,3-benzodioxole-5-yl)-quinazoline

https://huagongshe.com/de/reaction/217137

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloranilHCID 8371—
Edukt1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
Edukt2-(Aminomethyl)-4-nitroaniline hydrochlorideHCID 23085707—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-Nitro-2-(1,3-benzodioxole-5-yl)-quinazolineHCID 5786315682,5%

Reaktionsschritte

To a suspension of 5-nitro-2-amino-benzylamine hydrochloride (31 g, 0.152 mol) in DCM (450 ml) was added at 0° C. TEA (52.6 ml, 0.38 mol) and a solution of piperonyloyl chloride (27.3 g, 0.16 mol) in DCM (80 ml). The mixture was stirred for 2 hours at r.t. The solvent was removed i.v. and the residue triturated with ethanol/water 1/9, then with diisopropyl ether. The obtained solid was dried and suspended in toluene (900 ml) and POCl3 (670 ml). The mixture was heated at reflux for 2 hours, then the solvent was removed i.v. and the residue was triturated with water/ammonia, washed with water, dried over P2O5. A mixture of the obtained product and chloranil (32.7 g, 0.129 mol) in toluene (500 ml) was heated at reflux for 2 hours. The mixture was concentrated i.v. and the residue was triturated with NaOH 1M, washed with water and with methanol. The obtained solid was dried i.v. (37 g, 82.5% yield). C15H9N3O4, MW: 295.26, mp 220-222° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193353B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-808266bd50b44deb9e23ca3d7e66ac90
Quellennotizuspto-grants-2012_06