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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429026Erstellt: 24. Oktober 2026

2-chloro-N-phenylquinazolin-4-amine → N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride

https://huagongshe.com/de/reaction/429026

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-chloro-N-phenylquinazolin-4-amineHCID 317908—
Edukt4-Amino-N-methylbenzenemethanesulfonamideHCID 2778131—
LösungsmittelEthanolHCID 702—
LösungsmittelIsoamyl AlcoholHCID 31260—
ProduktN-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochlorideHCID 9825278—

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

A solution of 2-chloro-4-phenylamino-quinazoline (0.92 g) (prepared as described in Example 1a and N-methyl-(4-aminophenyl)-methanesulfonamide (0.80 g) in 10 ml of isopentylalcohol is stirred under nitrogen at 170° C. for 15 min in a sealed vessel. The warm reaction mixture is diluted with 10 ml ethanol and the hydrochloride salt, which is crystallizing on cooling, is filtered off to yield N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride as light yellow crystals melting at 259-263° C.; Rf (A2) 0.11, FAB-MS: (M+H)+=420. Analytical data: C22H21N5O2S+HCl.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06316203B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-500a0498b86745cab095443c4c237f6d
Quellennotizuspto-grants-2001_11