HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390099Generated: October 25, 2026
5-Nitroso-2,4,6-pyrimidinetriamine → tetra-Aminopyrimidine
https://huagongshe.com/reaction/1390099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Nitroso-2,4,6-pyrimidinetriamine | HCID 70504 | — |
| Reactant | Tetraaminopyrimidine sulfate | HCID 79358 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | tetra-Aminopyrimidine | HCID 70487 | — |
Reaction Steps
A process for preparing 2,4,5,6-tetraaminopyrimidine sulfate (TAPS) comprising (1) reacting about one molecular proportion of 5-nitroso-2,4,6-triaminopyrimidine (NTAP) in water with about 2.0 to 2.5 molecular proportions of zinc dust and about 4.0 to 4.7 molecular proportions of a suitable acid to provide a reaction mixture having a pH below 7; (2) reacting said reaction mixture at a temperature of about 20° to 65° C. to form the acid salt of 2,4,5,6-tetraaminopyrimidine; (3) adjusting the pH to about 2.0 to 2.5 by adding said acid to form a solution of said salt; (4) separating the insoluble materials from step (3) to obtain a wet cake and a mother liquor; (5) adding sulfuric acid to said mother liquor to adjust the pH to about 0.2 to 0.5 while maintaining the temperature at about 20° to 60° C.; (6) cooling the reaction mixture of step (5) to about 0° to 10° C. the precipitate 2,4,5,6-tetraaminopyrimidine sulfate; and (7) recovering said precipitate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04247693 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-e3cac4be84bf4edcbb55972bccfc9a62 |
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| Source note | uspto-grants-1981_01 |
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