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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706501Generated: October 27, 2026

Potassium Carbonate → N-(4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzyl)-5-iodo-3-nitropyridin-2-amine

https://huagongshe.com/reaction/706501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-iodo-3-nitropyridineHCID 1514294—
Reactant(4-(Cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamineHCID 118113995—
SolventAcetonitrileHCID 6342—
ProductN-(4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzyl)-5-iodo-3-nitropyridin-2-amineHCID 11811400058.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of (4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamine (2.50 g, 7.95 mmol) and potassium carbonate (1.41 g, 10.20 mmol) in acetonitrile (10 mL) was added 2-chloro-5-iodo-3-nitropyridine (2.90 g, 10.20 mmol). The resulting mixture was heated to 80° C. After 2 h, the mixture was filtered, and the filtrate was concentrated. Chromatographic purification of the residue (silica gel, 20% ethyl acetate in petroleum ether elute) afforded 2.60 g (58%) of N-(4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzyl)-5-iodo-3-nitropyridin-2-amine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174986B2
Source datasetuspto-grants-2015_11
ORD IDord-c21ddea1c366453eade9cbb9fb2d3674
Source noteuspto-grants-2015_11