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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944688Generated: October 31, 2026

Pyridine → 5-Bromo-2-(4-isopropylpiperazin-1-yl)benzothiazole

https://huagongshe.com/reaction/1944688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-IsopropylpiperazineHCID 78013—
Reactant5-Bromo-2-(methylthio)benzo[d]thiazoleHCID 2801271—
Product5-Bromo-2-(4-isopropylpiperazin-1-yl)benzothiazoleHCID 5958880077%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 5-bromo-2-(methylthio)benzothiazole (200 mg, 0.77 mmol), 1-isopropylpiperazine (985 mg, 7.7 mmol) and pyridine (610 mg, 7.7 mmol) was heated at 160° C. for 36 h. The reaction mixture was concentrated under reduced pressure and the residue was extracted with dichloromethane (3×10 mL). The combined organic extracts were washed with brine, dried (Na2SO4) and concentrated. The residue was purified by column chromatography on silica gel (eluent: 2% EtOAc in Petroleum ether) to give 200 mg (77%) of 5-bromo-2-(4-isopropylpiperazin-1-yl)benzothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394842B2
Source datasetuspto-grants-2013_03
ORD IDord-981fd4e095124cbf866dca6c462b877c
Source noteuspto-grants-2013_03