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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 409704Erstellt: 23. Oktober 2026

Dimethylamine → N,N,2-trimethylbenzo[d]thiazole-6-sulfonamide

https://huagongshe.com/de/reaction/409704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktHexaneHCID 8058—
EduktTriethylamineHCID 8471—
Edukt2-Methyl-1,3-benzothiazole-6-sulfonyl chlorideHCID 3583019—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN,N,2-trimethylbenzo[d]thiazole-6-sulfonamideHCID 1495122493%

Reaktionsschritte

A solution of Compound 2 (5.0 g, 20.2 mmol) from step (b) of Example 1 dissolved in tetrahydrofuran (THF, 30 ml) was added drop wise to a mixture of 2M N,N-dimethyl amine in THF (12 mL, 24.2 mmol) and triethylamine (5.6 ml, 40.4 mmol). The resultant mixture was stirred at room temperature for 3 hours. Solvents were removed by rotary evaporation and the residue thus obtained was partitioned between chloroform (100 ml) and water (100 ml). The organic layer was then washed with water (2×, 100 ml) and brine (1×, 100 ml), dried over sodium sulfate and evaporated. The oily residue thus obtained was dissolved in ca. 5 ml of hot ethyl acetate and this solution was then slowly added to 45 ml hexane. The mixture was cooled in the refrigerator overnight and the white solid that precipitated was collected, washed with hexane and dried to yield 4.8 g (93%) of Compound 24 whose structure is given below:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08759526B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-4ac7c52dee7b4688b920d3754a450e92
Quellennotizuspto-grants-2014_06