HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007117Generated: October 28, 2026
Dimethylformamide → N-(5-nitropyridin-2-yl) para-phenylenediamine
https://huagongshe.com/reaction/1007117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | p-Phenylenediamine, monohydrochloride | HCID 120279 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(5-nitropyridin-2-yl) para-phenylenediamine | HCID 24700317 | — |
Reaction Steps
Triethylamine (35 ml) was added into dimethylformamide (50 ml) including 2-chloro-5-nitropyridine (1) (9.5 g, 60 mmol) and para-phenylenediamine hydrochloride (10.9 g, 60 mmol), and stirred at the room temperature for 14 hours. After the reaction having been completed, the solution was poured into water, and the resultant solid was filtered and then N-(5-nitropyridin-2-yl) para-phenylenediamine was obtained as a brown solid. This solid was dissolved in ethanol (800 ml) and added with 5%-palladium carbon (2 g) so as to cause a hydrogen substitution, and then reduced at 70° C. under the normal pressure for 6 hours. After the reaction having been completed, the celite filtering was applied to remove the palladium carbon, and then it was washed by using a mixed solvent of ethyl acetate and hexane, thus obtained N-(5-amino-pyridin-2-yl) para-phenylenediamine (8.8 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794378B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-9f3add445076453383401c22a156d5df |
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| Source note | uspto-grants-2004_09 |
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