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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427351Generated: November 3, 2026

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

https://huagongshe.com/reaction/2427351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsoamyl NitriteHCID 8053—
Reactant5,7-Difluorobenzo[d]thiazol-2-amineHCID 15050564—
CatalystCupric ChlorideHCID 24014—
SolventAcetonitrileHCID 6342—
Product2-Chloro-5,7-difluorobenzo[D]thiazoleHCID 2198574748%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968576B2
Source datasetuspto-grants-2011_06
ORD IDord-3d252d53c1cf48359c6f364134e0ca4c
Source noteuspto-grants-2011_06