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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718137Generated: October 29, 2026

Potassium Iodide → HCID 90417450, compound

https://huagongshe.com/reaction/718137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantTert-Butyl nitriteHCID 10906—
Reactant4-((6-aminopyridin-3-yl)oxy)-N-methylpicolinamideHCID 90410540—
SolventDiiodomethaneHCID 6346—
SolventEthyl AcetateHCID 8857—
ProductHCID 90417450HCID 9041745036.8%

Reaction Steps

A mixture of 4-((6-aminopyridin-3-yl)oxy)-N-methylpicolinamide (0.4 g, 1.64 mmol) and potassium iodide (1.36 g, 8.19 mmol) in methylene iodide (5.46 mL) was treated dropwise with t-butylnitrite (1.95 mL, 16.4 mmol). The mixture was stirred overnight at RT, diluted with EtOAc (75 mL), and washed with 10% sodium carbonate (50 mL), 10% thiosulfate (50 mL), and brine (50 mL). The organics were dried over sodium sulfate, evaporated to dryness and purified by silica gel chromatography ((EtOAc/Hex) to afford 4-((6-iodopyridin-3-yl)oxy)-N-methylpicolinamide (0.214 g, 36.8%). 1H NMR (400 MHz, DMSO-d6): δ 8.78 (br d, J=5.6 Hz, 1H), 8.54 (d, J=5.6 Hz, 1H), 8.40 (d, J=3.0 Hz, 1H), 7.95 (d, J=8.6 Hz, 1H), 7.50 (dd, J=8.6, 3.1 Hz, 1H), 7.45 (d, J=2.6 Hz, 1H), 7.23 (dd, J=5.6, 2.7 Hz, 1H), 2.78 (d, J=4.9 Hz, 3H); MS (ESI) m/z: 356.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193719B2
Source datasetuspto-grants-2015_11
ORD IDord-722e9a26c4ce47dbb1b2690bdfcf1934
Source noteuspto-grants-2015_11