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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944652Generated: October 29, 2026

2-Chloro-6-methoxybenzothiazole → HCID 131730290, compound

https://huagongshe.com/reaction/1944652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methoxybenzothiazoleHCID 273132—
Reactant1-CyclopropylpiperazineHCID 4742004—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 131730290HCID 13173029018.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-6-methoxybenzothiazole (0.20 g, 1.0 mmol) and 1-cyclopropyl-piperazine (0.25 g, 2.0 mmol) was stirred at 120° C. overnight. The reaction mixture was allowed to cool and dissolved in a mixture of ethyl acetate a NaHCO3 solution. The phases were separated and the organic phase was washed with water (3×) and then extracted with 0.25 M hydrochloric acid (20 mL). The acidic aqueous extract was concentrated and re-evaporated with ethanol. The residue was crystallized from a mixture of ethanol and ethyl acetate to give 60 mg (18%) of 2-(4-cyclopropylpiperazin-1-yl)-6-methoxybenzothiazole, hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394842B2
Source datasetuspto-grants-2013_03
ORD IDord-2c9967c6d67446d6b7e20f9b7cfeec33
Source noteuspto-grants-2013_03