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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793162Generated: October 31, 2026

HCID 21936597, compound → HCID 10108776, compound

https://huagongshe.com/reaction/1793162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21936597HCID 21936597—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 10108776HCID 1010877694.5%

Reaction Steps

Tert-butyl 2-[2-(4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (9.35 g, 23.4 mmol) was suspended in 150 mL of 2M HCl in EtOH and the mixture was heated to reflux with stirring. After 2 h, the reaction was cooled to room temperature and the HCl salt of the product was collected by vacuum filtration and rinsed with ether. The free base was made by dissolving the HCl salt in water and treating with 10% NaOH solution until the mixture was pH 12. The aqueous suspension was extracted with CH2Cl2 (10×50 mL). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated to give 6.62 g of 1-[2-(2-aminoethoxy)ethyl]-2-ethyl-1H-imidazo[4,5-c]quinolin-4-amine as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078523B2
Source datasetuspto-grants-2006_07
ORD IDord-026743350d314774b776e8b50d32dafc
Source noteuspto-grants-2006_07