Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854073Generated: October 29, 2026

4-Nitrobenzaldehyde → HCID 178526539, compound

https://huagongshe.com/reaction/854073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
Reactant5-Nitropyridine-2,3-diamineHCID 3480151—
SolventNitrobenzeneHCID 7416—
ProductHCID 178526539HCID 17852653983%

Reaction Conditions

Temperature175 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256287B2
Source datasetuspto-grants-2007_08
ORD IDord-d4cb2141e51d46b5a89615ed0aeba23f
Source noteuspto-grants-2007_08