HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641474Generated: November 3, 2026
2,6-Diaminopyridine → HCID 57710474, compound
https://huagongshe.com/reaction/1641474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Diaminopyridine | HCID 8861 | — |
| Reactant | HCID 57710475 | HCID 57710475 | — |
| Reactant | HCID 71346087 | HCID 71346087 | — |
| Reactant | HCID 86630726 | HCID 86630726 | — |
| Solvent | Fuming sulfuric acid | HCID 24681 | — |
| Product | HCID 57710474 | HCID 57710474 | — |
| Product | HCID 57710475 | HCID 57710475 | — |
Reaction Steps
In a second embodiment, the present invention further comprises the composition 2,6-diamino-3-nitropyridine-5-sulfonic acid (DANPS). This is the intermediate formed during the process of the present invention described above, which is undesirable in the diaminodinitropyridine product. 2,6-Diamino-3-nitropyridine-5-sulfonic acid is prepared by dissolving 2,6-diaminopyridine or 2,6-diaminopyridine hemisulfate salt in oleum to form 2,6-diaminopyridine-3-sulfonic acid and treating the resulting solution with one stoichiometric amount of concentrated (98%) nitric acid. The resulting 2,6-diamino-3-nitropyridine-5-sulfonic acid is isolated by slowly drowning the reaction mix in an excess of 20% sulfuric acid followed by filtration, and washing the filter cake with water and 5% aqueous ammonium hydroxide solution and drying. 2,6-Diamino-3-nitropyridine-5-sulfonic acid is useful as a chemical intermediate, for instance as a dye intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08115007B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-43195309b1714c2cb2ff72b852df596d |
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| Source note | uspto-grants-2012_02 |
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