HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81943Generated: October 25, 2026
1,1-Dichloroethane → HCID 57557308, compound
https://huagongshe.com/reaction/81943
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | O-Desethyl Resiquimod | HCID 9817345 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57557308 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846710B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-d23cf62164bc4367aaacad1b5b0f406a |
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| Source note | uspto-grants-2014_09 |
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