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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262529Generated: November 2, 2026

Hydrochloric Acid → 5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/1262529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium DithioniteHCID 24489—
Reactant5-Amino-1,3-dipropylpyrimidine-2,4(1H,3H)-dioneHCID 19431565—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedioneHCID 509860560.8%

Reaction Steps

A mixture of 5-amino-1,3-dipropyl-2,4-(1H,3H)-pyrimidinedione (52.8 g, 0.25 moles), sodium nitrite (20.7 g, 0.30 moles) and water (1000 ml) is prepared and treated with hydrochloric acid (12 N, 30 ml, 0.35 moles) after the method of Blicke (J. Am. Chem. Soc., 76, 2798 (1954)]. 6-Amino-1,3-dipropyl-5-nitroso-2,4-(1H,3H)pyrmidinedione is collected as described and is used as obtained in the next step. The nitroso compound is suspended in water (500 ml) and treated with sodium dithionite, added portionwise in a quantity sufficient to effect decolorization of the purple nitroso compound. The resulting slurry is treated with sodium hydroxide (100 ml 50%), chilled, and filtered. The solids thus obtained are dried at 78° in a vacuum oven to yield 34.4 g of 5,6-diamino-1,3-dipropyl-2,4-(1H,3H)pyrimidinedione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452788
Source datasetuspto-grants-1984_06
ORD IDord-6297c7883cda4f6280283646b3e9d580
Source noteuspto-grants-1984_06