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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268815Generated: November 2, 2026

Triethylamine → HCID 9843452, compound

https://huagongshe.com/reaction/1268815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTLR7/8 agonist 3HCID 10380870—
SolventDichloromethaneHCID 6344—
ProductHCID 9843452HCID 984345254%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(2-Amino-2-methylpropyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinoline-4-amine (111 mg, 0.355 mmol) was dissolved in 5 ml of anhydrous CH2Cl2 and cooled to 0° C. under N2. To the stirred solution were added Et3N (99 μL, 0.71 mmol) and methanesulfonyl chloride (28 μL, 0.36 mmol) and the reaction was allowed to warm to ambient temperature overnight. The reaction mixture was then quenched by addition of saturated NaHCO3 solution (5 mL). The organic layer was separated and washed with H2O (2×5 mL) and brine, dried over Na2SO4 and concentrated under reduced pressure to give a tan foam. Purification by column chromatography (SiO2, 2.5%–5% MeOH/CHCl3) gave N-{2-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide (75 mg) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199131B2
Source datasetuspto-grants-2007_04
ORD IDord-8aa0f6237e644581a60f654991f0fd52
Source noteuspto-grants-2007_04