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HRID 907710Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Chloro-5,7-difluorobenzo[D]thiazole

https://huagongshe.com/de/reaction/907710

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIsoamyl NitriteHCID 8053—
Edukt5,7-Difluorobenzo[d]thiazol-2-amineHCID 15050564—
KatalysatorCupric ChlorideHCID 24014—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-Chloro-5,7-difluorobenzo[D]thiazoleHCID 2198574748%

Reaktionsschritte

To a solution containing copper chloride (II) (0.89 g, 6.64 mmol) and tri(ethylene glycol) dimethyl ether (6 mL) in acetonitrile (60 mL) was added isoamyl nitrite (0.97 g, 8.30 mmol) and the reaction mixture was stirred at rt for 30 minutes. To this suspension was added dropwise a solution of 5,7-difluoro-1,3-benzothiazol-2-amine (1.03 g, 5.53 mmol) in tri(ethylene glycol) dimethyl ether (20 mL) and acetonitrile (30 mL). The reaction mixture was stirred at rt for 10 minutes and heated at 50° C. for 2.5 h. The reaction mixture was cooled to rt, and then poured cautiously into cold aqueous 6 M HCl (400 mL). The solution was extracted with EtOAc. The organic layer was washed with HCl (1.0 M), water and brine, filtered, and concentrated. The residue was purified by flash chromatography (Biotage Flash 40M) using 5% ethyl acetate in hexane to afford 2-chloro-5,7-difluoro-1,3-benzothiazole (0.55 g, 48%). 1H NMR (400 MHz, CD2Cl2) 7.02 (m, 1H), 7.52 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08013166B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-24e6c5e3a1f94eb382fdcb143800b9b7
Quellennotizuspto-grants-2011_09