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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598034Generated: October 30, 2026

Methane → 1-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]-2-methylpropan-2-ol

https://huagongshe.com/reaction/598034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantN-{7-bromo-4-[(2-hydroxy-2-methylpropyl)amino][1,5]naphthyridin-3-yl}-3-methoxypropionamide hydrochlorideHCID 67052276—
SolventEthanolHCID 702—
SolventChloroform methanolHCID 21584188—
Product1-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]-2-methylpropan-2-olHCID 6705253073.6%

Reaction Steps

A mixture of N-{7-bromo-4-[(2-hydroxy-2-methylpropyl)amino][1,5]naphthyridin-3-yl}-3-methoxypropionamide hydrochloride (60.00 g, 138 mmol), potassium carbonate (60 g), water (300 mL), and ethanol (900 mL) was heated at reflux for 16 hours and then concentrated under reduced pressure. The precipitated solid was isolated by filtration, washed sequentially with water and methanol, and dried to provide a brown solid. This material was dissolved in a 3/1 mixture of chloroform/methanol and decolorized with activated charcoal to provide 38.5 g of 1-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]-2-methylpropan-2-ol as a white solid, mp 125° C. Anal. calcd for C16H19BrN4O2: % C, 50.67; % H, 5.05; % N, 14.77; Found: % C, 50.86; % H 4.94; % N, 15.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897609B2
Source datasetuspto-grants-2011_03
ORD IDord-e8d15552fb994b4aa9f9580d693a6a65
Source noteuspto-grants-2011_03