HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762226Generated: October 31, 2026
Hydrochloric Acid → 5-Nitroso-2,4,6-pyrimidinetriamine
https://huagongshe.com/reaction/1762226
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Nitroso-2,4,6-pyrimidinetriamine | HCID 70504 | 91% |
Reaction Steps
A solution of 70 g of sodium nitrite in 120 g of water was added dropwise at room temperature to a suspension of 66 g of malononitrile and 96 g of guanidine hydrochloride in 200 g of water, and the pH was kept at 4 by the addition of hydrochloric acid. After the reaction had continued for 4 hours at room temperature, 21 g of sodium carbonate and 400 g of dimethylformamide were added. The water was distilled off under reduced pressure. Thereafter, the reaction mixture was heated at 140° C. for 1 hour, isomerization to 5-nitroso-2,4,6-triamino-pyrimidine taking place. After the reaction was complete, 400 ml of water were added, and the product was filtered off and washed with water. After the product had been dried, 140 g of a pure raspberry-red 5-nitroso-2,4,6-triaminopyrimidine were obtained. The melting point of the product was above 340° C. and the yield was 91 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831139 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-23c0f39b4120411d90c15cad7efc8c69 |
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| Source note | uspto-grants-1989_05 |
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