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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1274146Erstellt: 25. Oktober 2026

2-Chloro-6,7-dimethoxy-4-quinazolinamine → 3-Amino-5-[N'-(4-amino-6,7-dimethoxy-quinazolin-2-yl)-hydrazino]-6-chloro-pyrazine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1274146

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
Edukt3-Amino-6-chloro-5-hydrazino-pyrazine-2-carboxylic acid methyl esterHCID 54167356—
LösungsmittelIsoamyl AlcoholHCID 31260—
Produkt3-Amino-5-[N'-(4-amino-6,7-dimethoxy-quinazolin-2-yl)-hydrazino]-6-chloro-pyrazine-2-carboxylic acid methyl esterHCID 4436188796,2%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Compound (51) (5 mmol) was added to a solution of 4-amino-2-chloro-6,7-dimethoxy quinazoline (0.96 g, 4 mmol) in isoamyl alcohol (10 mL) at 25° C. The mixture was then stirred at 120° C. for 12 h. After cooling to room temperature, the desired product was filtered and rinsed with acetone to give 1.62 g (96%) of the title compound: TLC (Rf =0.30; 10% CH3OH/CH2Cl2); 1H NMR (DMSO) δ 11.90 (br, 1H), 10.30 (br, 1H), 9.80 (br, 1H), 9.00 (br, 1H), 8.80 (br, 1H), 7.80 (s, 1H), 7.69 (d, 1H, J=2.0), 7.41 (s, 1H), 7.19 (s, 1H), 3.86 (s, 3H), 3.85 (s, 3H), 3.76 (s, 3H); HRMS (FAB) m/z 421.1152 (M+H)+ (C16H18N8O4Cl requires 421.1110); Anal. (C16H18N8O4Cl·1/4CH3OH) C, H, N.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06156758
Quelldatensatzuspto-grants-2000_12
ORD IDord-a7aa2f44b54b44b59dc4c8b9c4d396bd
Quellennotizuspto-grants-2000_12