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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353133Erstellt: 24. Oktober 2026

Di-tert-butyl dicarbonate → 4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamide

https://huagongshe.com/de/reaction/353133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDi-tert-butyl dicarbonateHCID 90495—
Edukt3-IsopropylanilineHCID 458679—
Edukt6,7-Dimethoxy-4-piperazin-1-yl-quinazolineHCID 2758484—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamideHCID 2270745163%

Reaktionsschritte

To a solution of 2.05 g (9.39 mmol) of di-tert-butyl dicarbonate in 30 ml of dichloromethane was added 108 mg (0.88 mmol) of 4-(N,N-dimethylamino)pyridine. After the mixture was stirred at room temperature for 5 minutes, 1.26 ml (8.95 mmol) of 3-isopropylaniline was added thereto, followed by further stirring at room temperature for 30 minutes. To the reaction mixture was added 548 mg (2.00 mmol) of 6,7-dimethoxy-4-piperazinylquinazoline obtained by the method described in South African Patent No. 67 06512 (1968), followed by stirring at room temperature for 30 minutes. After the solvent was evaporated, the residue was purified by silica gel chromatography and recrystallized from ethyl acetate to give the desired compound as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750218B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-bb64dae8372d4097a20658a543248991
Quellennotizuspto-grants-2004_06