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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 5-Amino-1,3-dipropylpyrimidine-2,4(1H,3H)-dione | HCID 19431565 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione | HCID 5098605 | 60.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04452788 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-6297c7883cda4f6280283646b3e9d580 |
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| Source note | uspto-grants-1984_06 |
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