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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444972Generated: October 26, 2026

1-Allylpiperazine → N-[6-(4-Allylpiperazin-1-yl)pyrimidin-4-yl]-4-isopropylbenzenesulfonamide

https://huagongshe.com/reaction/444972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AllylpiperazineHCID 806422—
ReactantHCID 86003781HCID 86003781—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-[6-(4-Allylpiperazin-1-yl)pyrimidin-4-yl]-4-isopropylbenzenesulfonamideHCID 69145389—

Reaction Steps

430 mg (1.38 mmol) of N-(6-chloropyrimidin-4-yl)-4-isopropylbenzenesulfonamide from Example 18.1 were dissolved in 3 ml of dimethyl sulfoxide, after which 1.74 g (13.79 mmol) of N-allylpiperazine were added and the mixture was stirred overnight. Subsequently, the reaction mixture was stirred at 100° C., in a microwave oven, for 45 minutes. After the reaction mixture had cooled down to room temperature, it was diluted with 50 ml of water. After that, the aqueous reaction mixture was extracted with 50 ml of ethyl acetate and the precipitate was filtered off with suction, with 190 mg (34% of theory) of the title compound being obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476275B2
Source datasetuspto-grants-2013_07
ORD IDord-5c3dbaeeb53b4a388bda7136820bad7f
Source noteuspto-grants-2013_07