HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854073Generated: October 29, 2026
4-Nitrobenzaldehyde → HCID 178526539, compound
https://huagongshe.com/reaction/854073
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | 5-Nitropyridine-2,3-diamine | HCID 3480151 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 178526539 | HCID 178526539 | 83% |
Reaction Steps
To a stirred solution of 2,3-diamino-5-nitropyridine (3) (400 mg, 2.6 mmol) in nitrobenzene (50 mL) was added 4-nitrobenzaldehyde (393 mg, 2.6 mmol) and the mixture heated at 175° C. for 24 h. The solvent was removed by distillation under reduced pressure and the resulting orange solid collected by filtration using CH3CN. The filter cake was washed with ether and air dried to give 4 as an orange solid (0.614 g, 2.1 mmol, 83%) that was used as is without further purification. 1H NMR (500 MHz, DMSO-d6) δ14.58 (br s, 1H), 9.28 (apparent d, 1H), 8.88 (br s, 1H), 8.51 (d, J=8.39 Hz, 2H), 8.45 (d, J=8.28 Hz, 2H). EIMS M−1 284.3. Rf=0.55 (silica, 19:1 DCM/MeOH)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256287B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-d4cb2141e51d46b5a89615ed0aeba23f |
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| Source note | uspto-grants-2007_08 |
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