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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259861Erstellt: 26. Oktober 2026

Benzene → 4-(2-chlorophenyl)-6,8-dimethyl-3-(3-methyl-4H-1,4-benzothiazin-2-carbonyl) aminoquinoline

https://huagongshe.com/reaction/259861

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
Edukt2-AminothiophenolHCID 8713—
EduktDiketeneHCID 12661—
Edukt3-Amino-4-(2-chlorophenyl)-6,8-dimethylquinolineHCID 10446536—
KatalysatorTriethylamineHCID 8471—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt4-(2-chlorophenyl)-6,8-dimethyl-3-(3-methyl-4H-1,4-benzothiazin-2-carbonyl) aminoquinolineHCID 2317011226%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A mixture of 3-amino-4-(2-chlorophenyl)-6,8-dimethylquinoline (1.0 g), triethylamine (2 drops) and benzene (5 ml) was heated to 70° C., and diketene (0.25 ml) was dropwise added thereto. The mixture was further heated at 70° C. for 30 minutes, and then, dimethylsulfoxide (15 ml) and 2-aminothiophenol (0.4 g) were added thereto. The resultant mixture was heated at 130° C. for an hour, diluted with water and extracted with ethyl acetate. The ethyl acetate layer was washed with a solution of salt and dried (MgSO4). The solvent was removed and the residue was purified by a silica gel column chromatography with hexane-ethyl acetate (3:1,V/V), and then crystallized from ethyl acetate-ethyl ether to give 4-(2-chlorophenyl)-6,8-dimethyl-3-(3-methyl-4H-1,4-benzothiazin-2-ylcarbonyl) aminoquinoline (0.39 g, 26%) as yellowish prisms.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05523407
Quelldatensatzuspto-grants-1996_06
ORD IDord-47bfbe8bf51245bd94ad44f64906fae9
Quellennotizuspto-grants-1996_06