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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262527Generated: October 25, 2026

Hydrochloric Acid → 4-(1,3-dipropyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid potassium salt

https://huagongshe.com/reaction/1262527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedioneHCID 5098605—
ReactantPotassium 4-carboxybenzenesulfonateHCID 23670833—
SolventWaterHCID 962—
Product4-(1,3-dipropyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid potassium saltHCID 2370272017%

Reaction Steps

A mixture of 5,6-diamino-1,3-dipropyl-2,4-(1H,3H)pyrimidinedione (16.0 g, 0.07 moles), 4-sulfobenzoic acid monopotassium salt (17.0 g, 0.0707 moles) and water (250 ml) is prepared, and the pH adjusted to 5.0 by the addition of 10% potassium hydroxide. To this solution is added ethyl-3-(3-dimethylaminopropyl)carbodiimide (13.6 g, 0.0707 moles) in one portion, and the pH maintained at 5.0±0.5 by the dropwise addition of 4 N hydrochloric acid. When the pH stabilizes, the reaction mixture is treated with sodium hydroxide (100 ml, 50%), boiled under reflux for ten minutes, treated with activated carbon, and filtered warm. The resulting solution is chilled in ice, treated with hydrochloric acid (12 N, 1350 ml), and filtered. The solids are dried, recrystallized from methanol, and dried at 78° to yield 5.12 grams of 4-(1,3-dipropyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid potassium salt, mp greater than 360°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452788
Source datasetuspto-grants-1984_06
ORD IDord-faa238c7a27a42e7abd425e4be929a7a
Source noteuspto-grants-1984_06