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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262523Generated: November 2, 2026

Thionyl Chloride → 1,3-Diethyl-8-[4-(4-methyl-piperazine-1-sulfonyl)-phenyl]-3,7-dihydro-purine-2,6-dione

https://huagongshe.com/reaction/1262523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-MethylpiperazineHCID 53167—
Reactant4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acidHCID 15587300—
SolventDimethylformamideHCID 6228—
Product1,3-Diethyl-8-[4-(4-methyl-piperazine-1-sulfonyl)-phenyl]-3,7-dihydro-purine-2,6-dioneHCID 1558730781.9%

Reaction Steps

A mixture of 4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid (5.0 g, 0.014 moles) and N,N-dimethylformamide (150 ml) is cooled to 0° and treated with thionyl chloride (3.3 g, 0.027 moles). When the addition is complete, the reaction mixture is permitted to warm to ambient temperature and stirred vigorously until a thick slurry results. To this slurry is added N-methylpiperazine (13.7 g, 0.137 moles) in one portion, the mixture is stirred until a clear solution is obtained, and concentrated on a rotary evaporator. The residue is taken up in water, filtered, recrystallized from ethanol, and dried at 48° to yield 5.12 grams of 1-[[4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)phenyl]sulfonyl]4-methylpiperazine, mp 305°-307° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452788
Source datasetuspto-grants-1984_06
ORD IDord-00f000f3c47d4b03b7983fd1f44db36d
Source noteuspto-grants-1984_06