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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81943Generated: October 25, 2026

1,1-Dichloroethane → HCID 57557308, compound

https://huagongshe.com/reaction/81943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantAcetyl chlorideHCID 6367—
ReactantO-Desethyl ResiquimodHCID 9817345—
SolventPyridineHCID 1049—
ProductHCID 57557308HCID 57557308—

Reaction Steps

To a round-bottomed flask with stir bar was added 1-(4-amino-2-hydroxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol (1 g, 3.5 mmol) followed by dichloroethane (20 mL) and pyridine (3 mL). To the stirred suspension was added acetyl chloride (0.27 mL, 1.1 equivalents) and the reaction was stirred at ambient temperature for 30 min. The solvent was evaporated under reduced pressure to afford a solid. The product was isolated by two purifications by prep HPLC (ISCO Combiflash Separation System, Biotage Si 40+M column, eluted with a gradient of 0-7% methanol in dichloromethane with 1% ammonium hydroxide) to provide [4-amino-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]methyl acetate as an off white solid (130 mg), mp 203-205° C.; MS (ESI) m/z 329 (M+H); Anal. Calcd for C17H20N4O3.0.25CH4O: C, 61.59; H, 6.29; N, 16.66. Found C, 61.24; H, 6.22; N, 16.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846710B2
Source datasetuspto-grants-2014_09
ORD IDord-d23cf62164bc4367aaacad1b5b0f406a
Source noteuspto-grants-2014_09