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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369352Generated: October 30, 2026

3-Aminopyridine → HCID 22598273, compound

https://huagongshe.com/reaction/1369352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2,2,6,6-Tetramethylpiperidin-1-olHCID 549976—
SolventPyridineHCID 1049—
ProductHCID 22598273HCID 2259827351.2%

Reaction Steps

The procedure of Example 1 is repeated using 1.95 g (12.5 mmol) of 1-oxyl-2,2,6,6-tetramethylpiperidine, 3.90 g (38 mmol) of tert-butyl nitrite, 7.6 mg (0.0125 mmol) of (S,S)-(+)-N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 120 mL of pyridine and 2.35 g (25 mmol) of 3-aminopyridine at 70° C. The crude product obtained is purified by vacuum flash chromatography (heptane) to give 1.5 g of the title compound as a colorless oil in 50.8% yield. The structure is confirmed by 1Hnmr and mass spectrographic analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579328B2
Source datasetuspto-grants-2003_06
ORD IDord-7e2e83b2f9914d18be4d73c1caa9d966
Source noteuspto-grants-2003_06