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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411227Generated: October 27, 2026

Hydrogen Bromide → HCID 83698021, compound

https://huagongshe.com/reaction/2411227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
Reactant1-(4,6-Dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazineHCID 71252181—
SolventAcetic AcidHCID 176—
ProductHCID 83698021HCID 8369802162.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 5-amino-2,4-dimethylpyridine (883 mg) were added N,N-diisopropylethylamine (2.1 mL) and N,N-bis(2-chloroethyl)-p-toluenesulfonamide (2.08 g), and the mixture was stirred with heating under reflux. After completion of the reaction, water was added to the reaction mixture, the mixture was extracted with chloroform, and the solvent was evaporated. The obtained residue was purified by column chromatography (chloroform:methanol) to give 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg). The obtained 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg) was dissolved in acetic acid (2 mL), 40% hydrobromic acid (2 mL) was added, and the mixture was stirred at 100° C. After completion of the reaction, the reaction mixture was neutralized with aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The solvent was evaporated from the organic layer to give the title compound (131 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-567da05e6a364c3f873dd3bbccd9f107
Source noteuspto-grants-2014_08