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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006636Generated: October 31, 2026

Ammonia → 1-(4-Amino-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol

https://huagongshe.com/reaction/1006636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantN-[2-Chloro-4-(2-hydroxy-2-methylpropyl)amino-3-quinolinyl]-3-methoxypropanamideHCID 22672655—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product1-(4-Amino-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-olHCID 10086179—

Reaction Conditions

Temperature150 °C

Reaction Steps

N-[2-Chloro-4-(2-hydroxy-2-methylpropyl)amino-3-quinolinyl]-3-methoxypropanamide (6 g, Example 110) was added to 5% ammonia in methanol (60 mL). The mixture was heated in a Parr bomb for 5 hours at approximately 150° C. The solvent was evaporated under vacuum to give a brown residue. The residue was diluted with water and sodium bicarbonate then extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over magnesium sulfate then evaporated to provide a tan solid. The solid was purified by silica gel chromatography to provide 1.64 g of the desired product as a solid, m.p. 174-175° C. Analysis: Calculated: %C, 65.0; %H, 7.0; %N, 17.8; Found: %C, 64.8; %H, 7.0; %N, 17.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790961B2
Source datasetuspto-grants-2004_09
ORD IDord-2120041e2e30474386919eb922a341d3
Source noteuspto-grants-2004_09