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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798873Generated: November 3, 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/1798873

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 numberUS08343993B2
Source datasetuspto-grants-2013_01
ORD IDord-077dd8d27e90400fb013dfd695703e24
Source noteuspto-grants-2013_01