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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505391Generated: October 25, 2026

N-Iodosuccinimide → 5-Iodo-6-methoxy-3-nitropyridin-2-amine

https://huagongshe.com/reaction/505391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Amino-6-methoxy-3-nitropyridineHCID 3852428—
SolventAcetic AcidHCID 176—
Product5-Iodo-6-methoxy-3-nitropyridin-2-amineHCID 5735492899%

Reaction Steps

A suspension of 6-methoxy-3-nitro-2-pyridineamine (14.6 g, 86.4 mmol) and N-iodosuccinimide (29.2 g, 130 mmol) in acetic acid (280 ml) was stirred at room temperature for 21 hours and 30 minutes. The reaction mixture was concentrated and the residue was dissolved in ethyl acetate and 0.5N sodium hydroxide. The ethyl acetate layer was washed with a saturated sodium bicarbonate solution and a saturated brine solution, dried over anhydrous sodium sulfate, and concentrated. The residue was suspended in hexane, and a resulted precipitate was filtered and washed with hexane, thereby yielding the title compound (25.2 g, 85.5 mmol, 98.9%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781452B2
Source datasetuspto-grants-2010_08
ORD IDord-635e35f98e904c50ac3f494a9cf36466
Source noteuspto-grants-2010_08