HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-chloro-N-phenylquinazolin-4-amine → N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-chloro-N-phenylquinazolin-4-amine | HCID 317908 | — |
| Edukt | 4-Amino-N-methylbenzenemethanesulfonamide | HCID 2778131 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Isoamyl Alcohol | HCID 31260 | — |
| Produkt | N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride | HCID 9825278 | — |
Reaktionsbedingungen
| Temperatur | 170 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06316203B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-500a0498b86745cab095443c4c237f6d |
| Quellennotiz | uspto-grants-2001_11 |