Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583906Generated: October 30, 2026

Triethylamine → HCID 9843452, compound

https://huagongshe.com/reaction/583906

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 numberUS06924293B2
Source datasetuspto-grants-2005_08
ORD IDord-177ecfeaa71c4fdf8f0a7f91f3baad60
Source noteuspto-grants-2005_08